Macroheterocyclic Compounds - a Key Building Block in New Functional Materials and Molecular Devices

Cite as

Koifman O.I., Ageeva T.A., Beletskaya I.P., Averin A.D., Yakushev A.A., Tomilova L.G.,.Dubinina T.V., Tsivadze A.Yu., Gorbunova Yu.G., Martynov A.G., Konarev D.V., Khasanov S.S., Lyubovskaya R.N., Lomova T.N., Korolev V.V., Zenkevich E.I., Blaudeck T. , Ch. von Borczyskowski, Zahn D.R.T., Mironov A.F., Bragina N.A., Ezhov A.V., Zhdanova K.A., Stuzhin P.A., Pakhomov G.L., Rusakova N.V., Semenishyn N.N., Smola S.S., Parfenyuk V.I., Vashurin A.S., Makarov S.V., Dereven’kov I.A., Mamardashvili N.Zh., Kurtikyan T.S., Martirosyan G.G., Burmistrov V.А., Aleksandriiskii V.V., Novikov I.V., Pritmov D.A., Grin M.A., Suvorov N.V., Tsigankov A.A., Fedorov A.Yu., Kuzmina N.S., Nyuchev A.V., Otvagin V.F., Kustov A.V., Belykh D.V., Berezin D.B., Solovieva A.B., Timashev P.S., Milaeva E.R., Gracheva Yu.A., Dodokhova M.A., Safronenko A.V., Shpakovsky D.B., Syrbu S.A., Gubarev Yu.A., Kiselev A.N., Koifman M.O., Lebedeva N.Sh., Yurina E.S. Macroheterocyclic Compounds – a Key Building Block in New Functional Materials and Molecular Devices Macroheterocycles 2020, 13, 311-467, DOI: 10.6060/mhc200814k

Oskar I. Koifman,^a,b@1 Tatyana A. Ageeva,^a Irina P. Beletskaya,^c,d@2 Alexei D. Averin,^c,d Alexei A. Yakushev,^c Larisa G. Tomilova,^c,e@3 Tatiana V. Dubinina,^c,e Aslan Yu. Tsivadze,^d,f Yulia G. Gorbunova,^d,f Alexander G. Martynov,^d@4 Dmitri V. Konarev,^g@5 Salavat S. Khasanov,^h Rimma N. Lyubovskaya,^g Tatyana N. Lomova,^b@6 Viktor V. Korolev,^b Eduard I. Zenkevich,^i@7 Thomas Blaudeck,^j,k Christian von Borczyskowski,^l Dietrich R.T. Zahn,^k,l Andrey F. Mironov,^m@8 Natal’ya A. Bragina,^m Artem V. Ezhov,^m@9 Kseniya A. Zhdanova,^m Pavel A. Stuzhin,^a@10 Georgy L. Pakhomov,ⁿ Nataliya V. Rusakova,^o@11 Nikolay N. Semenishyn,^o Sergey S. Smola,^o Vladimir I. Parfenyuk,^b@12 Arthur S. Vashurin,^a@13 Sergei V. Makarov,^a Ilia A. Dereven’kov,^a@14 Nugzar Zh. Mamardashvili,^b@15 Tigran S. Kurtikyan,^p Garik G. Martirosyan,^p@16 Vladimir А. Burmistrov,^a@17 Viktor V. Aleksandriiskii,^a Igor V. Novikov,^a Dmitriy A. Pritmov,^m Mikhail A. Grin,^m@18 Nikita V. Suvorov,^m Anatoliy A. Tsigankov,^q Alexey Yu. Fedorov,^r@19 Natalia S. Kuzmina,^r Alexander V. Nyuchev,^r Vasilii F. Otvagin,^r Andrey V. Kustov,^a,b Dmitry V. Belykh,^s Dmitry B. Berezin,^a@20 Anna B. Solovieva,^t@21 Peter S. Timashev,^t,u Elena R. Milaeva,^c@22 Yulia A. Gracheva,^c Margarita A. Dodokhova,^v Andrei V. Safronenko,^v Dmitry B. Shpakovsky,^c Sergey A. Syrbu,^b Yury A. Gubarev,^b@23 Alexey N. Kiselev,^b Mikhail O. Koifman,^a Natalia Sh. Lebedeva,^b and Elena S. Yurina^b

Dedicated to the 90th Anniversary of Ivanovo State University of Chemistry and Technology

^aResearch Institute of Macroheterocyclic Compounds, Ivanovo State University of Chemistry and Technology, 153000 Ivanovo, Russia

^bG.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences, 153045 Ivanovo, Russia

^cDepartment of Chemistry, M.V. Lomonosov Moscow State University, 119991 Moscow, Russia

^dA.N. Frumkin Institute of Physical Chemistry and Electrochemistry, 119991 Moscow, Russia

^eInstitute of Physiologically Active Compounds of the Russian Academy of Sciences, 142432 Chernogolovka, Moscow Region, Russia

^fN.S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russia

^gInstitute of Problems of Chemical Physics of the Russian Academy of Sciences, 142432 Chernogolovka, Moscow region, Russia

^hInstitute of Solid State Physics of the Russian Academy of Sciences, 142432 Chernogolovka, Moscow region, Russia

ⁱBelarussian National Technical University, 220013 Minsk, Belarus

^jFraunhofer Institute for Electronic Nano Systems (ENAS), Technologie-Campus 3, 09126 Chemnitz, Germany

^kChemnitz University of Technology, Research Center for Materials, Architectures and Integration of Nanomembranes (MAIN), 09107 Chemnitz, Germany

^lChemnitz University of Technology, Institute of Physics, 09107 Chemnitz, Germany

^mMIREA-Russian Technological University, 119454 Moscow, Russia

ⁿInstitute for Physics of Microstructures of the Russian Academy of Sciences, GSP-105, 603950 Nizhny Novgorod, Russia

^oA.V. Bogatsky Physico-Chemical Institute of the National Academy of Sciences of Ukraine, 65080 Odessa, Ukraine

^pScientific Technological Center of Organic and Pharmaceutical Chemistry NAS RA, Molecule Structure Research Centre, 0014 Yerevan, Armenia

^qInstitute of Biology Fundamental Problems of the Russian Academy of Sciences,142290 Pushchino, Moscow region, Russia

^rN.I. Lobachevsky State University of Nizhny Novgorod, 603950 Nizhny Novgorod, Russia

^sInstitute of Chemistry of Komi Republic Scientific Center of Russian Academy of Sciences, 167000 Syktyvkar, Russia

^tN.N. Semenov Federal Research Center for Chemical Physics of the Russian Academy of Sciences, 119991 Moscow, Russia

^uInstitute for Regenerative Medicine, I.M. Sechenov University, 119991 Moscow, Russia

^vRostov State Medical University, 344022 Rostov-on-the-Don, Russia

Corresponding authors E-mails: ^@1koifman@isuct.ru; ^@2beletska@org.chem.msu.ru; ^@3tom@med.chem.msu.ru; ^@4Martynov.Alexandre@gmail.com; ^@5konarev3@yandex.ru; ^@6tnl@isc-ras.ru; ^@7zenkev@tut.by;^@8mironov@mitht.ru; ^@9artem.ejov@gmail.com; ^@10stuzhin@isuct.ru; ^@11natavrusakova@gmail.com; ^@12vip@isc-ras.ru; ^@13asvashurin@mail.ru; ^@14derevenkov@gmail.com; ^@15ngm@isc-ras.ru; ^@16ggmartirosyan@gmail.com; ^@17burmistrov@isuct.ru; ^@18michael_grin@mail.ru; ^@19afedorovnn@yandex.ru; ^@20berezin@isuct.ru; ^@21ann.solovieva@gmail.com; ^@22milaeva@med.chem.msu.ru; ^@23yury.gu@gmail.com

DOI: 10.6060/mhc200814k
Macroheterocycles 2020 13(4) 311-467

The review discusses the latest advances in the directed synthesis and application of macroheterocyclic compounds in science, engineering and technology, viz. as catalysts for various processes in photo- and electrocatalysis, optical chemosensors for metal cations, selective receptors of organic compounds, inductors and selectors, in nonlinear optics, organic electronics, as magnets, photosensitizers for PDT of a number of oncological diseases and for antimicrobial PDT, etc.

References:

Click here to expand or collapse this section

1. Milgrom L.R. The Colours of Life: An Introduction to the Chemistry of Porphyrins and Related Compounds. Oxford: University Press, 1997. 256 p.

2. Battersby A.R. Nat. Prod. Rep. 2000, 17, 507-526.
https://doi.org/10.1039/b002635m

3. Tetrapyrroles: Birth, Life and Death (Warren M.J., Smith A.G., Ed.) N.Y.: Springer Science & Business Media, 2009. 406 p.

4. Serebrennikova O.V. Geochemistry of Porphyrins: Conditions of Accumulation and Direction of Metalloporphyrin Transformation in Sendimentary Rocks. In: Advances in Porphyrin Chemistry. Vol. 3. (Golubchikov O.A., Ed.) SPb.: St-PbGU, 2001. p. 326-349.

5. Keely B.J. Geochemistry of Chlorophylls. In: Chlorophylls and Bacteriochlorophylls. Advances in Photosynthesis and Respiration. Vol. 25. (Grimm B., Porra R.J., Rüdiger W., Scheer H., Ed.) Netherlands: Springer, 2006. р. 535-561.
https://doi.org/10.1007/1-4020-4516-6_37

6. Bandaranayake W.M. Nat. Prod. Rep. 2006, 23, 223-255.
https://doi.org/10.1039/b307612c

7. Kepp K.P. Coord. Chem. Rev. 2017, 344, 363-374.
https://doi.org/10.1016/j.ccr.2016.08.008

8. Collman J.P., Boulatov R., Sunderland C.J, Fu L. Chem. Rev. 2004, 104, 561-588.
https://doi.org/10.1021/cr0206059

9. Anderson J.L.R., Chapman S.K. Dalton Trans. 2005, 13-24.
https://doi.org/10.1039/b413046d

10. Bertini I., Cavallaro G., Rosato A. Chem. Rev. 2006, 106, 90-115.
https://doi.org/10.1021/cr050241v

11. Dereven'kov I.A., Salnikov D.S., Silaghi-Dumitrescu R., Makarov S.V., Koifman O.I. Coord. Chem. Rev. 2016, 309, 68-83.
https://doi.org/10.1016/j.ccr.2015.11.001

12. Saga Y., Yamashita M., Imanishi M., Kimura Y., Masaoka Y., Hidaka T., Nagasawa Y. ACS Omega 2020, 5, 6817−6825.
https://doi.org/10.1021/acsomega.0c00152

13. Lindsey J.S. Chem. Rev. 2015, 115, 6534-6620.
https://doi.org/10.1021/acs.chemrev.5b00065

14. Malyasova A.S., Khelevina O.G., Koifman O.I. Ross. Khim. Zh. 2017, 61, 3-10.

15. Krasnovsky Jr. А.А. Ross. Khim. Zh. 2017, 61, 17-41.

16. Scheer H. An Overview of Chlorophylls and Bacteriochlorophylls: Biochemistry, Biophysics, Functions and Applications. In: Chlorophylls and Bacteriochlorophylls. Advances in Photosynthesis and Respiration. Vol. 25. (Grimm B., Porra R.J., Rüdiger W., Scheer H., Eds.) Netherlands: Springer, 2006. p. 1-26.
https://doi.org/10.1007/1-4020-4516-6_1

17. Gunderson V.L., Wasielewski M.R. Supramolecular Chlorophyll Assemblies for Artificial Photosynthesis. In: Handbook of Porphyrin Science. Vol. 20. (Kadish K.M., Smith K.M., Guilard R., Eds.) World Scientific Publishing Co. Pte. Ltd.: Singapore, 2012. p. 45-105.
https://doi.org/10.1142/9789814335508_0022

18. Borbas K.E. Chlorins. In: Handbook of Porphyrin Science. Vol. 36. (Kadish K.M., Smith K.M., Guilard R., Eds.) World Scientific Publishing Co. Pte. Ltd.: Singapore, 2016. p. 1-149.

19. Storz J.F. Physiology 2016, 31, 223-232.
https://doi.org/10.1152/physiol.00060.2015

20. Yonetani T., Kanaori K. Biochim. Biophys. Acta 2013, 1834, 1873-1884.
https://doi.org/10.1016/j.bbapap.2013.04.026

21. Wilks A. Antioxidants & Redox Signaling 2002, 4, 603-614.
https://doi.org/10.1089/15230860260220102

22. Rovira C., Kunc K., Hutter J., Parrinello M. Inorg. Chem. 2001, 40, 11-17.
https://doi.org/10.1021/ic000143m

23. Jones A.R. Photochem. Photobiol. Sci. 2017, 16, 820-834.
https://doi.org/10.1039/C7PP00054E

24. Shell T.A., Lawrence D.S. Acc. Chem. Res. 2015, 48, 11, 2866-2874. https://doi.org/10.1021/acs.accounts.5b00331

25. Proinsias K., Giedyk M., Gryko D. Chem. Soc. Rev. 2013, 42, 6605-6619.
https://doi.org/10.1039/c3cs60062a

26. Ishihara S., Labuta J., Van Rossom W., Ishikawa D., Minami K., Hill J.P., Ariga K. Phys. Chem. Chem. Phys. 2014, 16, 9713-9746.
https://doi.org/10.1039/c3cp55431g

27. Mirkovic T., Ostroumov E.E., Anna J.M., van Grondelle R., Govindjee, Scholes G.D. Chem. Rev. 2017, 117, 249-293.
https://doi.org/10.1021/acs.chemrev.6b00002

28. Aratani N., Kim D., Osuka A. Acc. Chem. Res. 2009, 42, 1922-1934.
https://doi.org/10.1021/ar9001697

29. Otsuki J. J. Mater. Chem. A 2018, 6, 6710-6753.
https://doi.org/10.1039/C7TA11274B

30. Liu Y., Zhang S., Lindsey J.S. Nat. Prod. Rep. 2018, 35, 879-901.
https://doi.org/10.1039/C8NP00020D

31. Taniguchi M., Lindsey J.S. Chem. Rev. 2017, 117, 344-535.
https://doi.org/10.1021/acs.chemrev.5b00696

32. Dudkin S.V., Makarova E.A., Lukyanets E.A. Russ. Chem. Rev. 2016, 85, 700-730.
https://doi.org/10.1070/RCR4565

33. Chen C.-Y., Sun E., Fan D., Taniguchi M., McDowell B.E., Yang E., Diers J. R., Bocian D.F., Holten D., Lindsey J.S. Inorg. Chem. 2012, 51, 9443-9464.
https://doi.org/10.1021/ic301262k

34. Brückne C., Samankumara L., Ogikubo J., Syntheses of Bacteriochlorins and Isobacteriochlorins. In: Handbook of Porphyrin Science. Vol. 17. (Kadish K.M., Smith K.M., Guilard R., Eds.) Singapore: World Scientific Publishing Co. Pte. Ltd., 2012. p. 1-112.
https://doi.org/10.1142/9789814335508_0003

35. Szyszko B., Latos-Grażyński L. Chem. Soc. Rev. 2015, 44, 3588-3616.
https://doi.org/10.1039/C4CS00398E

36. Berezin D.B., Karimov D.R., Kustov A.V. Corrols and Their Derivatives: Synthesis, Properties, and Prospects for Practical Application. (Koifman O.I., Ed.) M.: LENAND, 2018. 304 p.

37. Paolesse R. Synthesis and Modification of Porphyrinoids. In: Topics in Heterocyclic Chemistry. Vol. 33. Springer-Verlag: Berlin, 2014. p. 1-34.
https://doi.org/10.1007/978-3-642-38533-9

38. Barata J.F.B., Neves M.G.P.M.S., Faustino M.A.F., Tomé A.C., Cavaleiro J.A.S. Chem. Rev. 2017, 117, 3192-3253.
https://doi.org/10.1021/acs.chemrev.6b00476

39. Porphyrins: Structure, Properties, Synthesis (Enikolopjan N.S., Ed.) M: Nauka, 1985. 333 p.

40. Askarov K.A., Ageeva T.A., Rashidova S.T. Wastes of Sericulture. Ways of Their Processing, Application Prospects (O.I. Koifman, Ed.) M.: Khimia, 2008. 219 р.

41. Mironov A.F. Rossiiskii Khimicheskii Zhurnal 2017, 61, 42-68.

42. Grin M.A., Mironov A.F. Rus. Chem. Bull., Int. Ed. 2016, 65, 333-349.
https://doi.org/10.1007/s11172-016-1307-1

43. Nyuchev A.V., Otvagin V.F., Gavryushin A.E., Romanenko Yu.I., Koifman O.I., Belykh D.V., Schmalz H.-G., Fedorov A.Yu. Synthesis 2015, 47, 3717-3726.
https://doi.org/10.1055/s-0034-1378876

44. Otvagin V.F., Nyuchev A.V., Kuzmina N.S., Grishin I.D., Gavryushin A.E., Romanenko Yu.V., Koifman O.I., Belykh D.V., Peskova N.N., Shilyagina N.Yu., Balalaeva I.V., Fedorov A.Yu. Eur. J. Med. Chem. 2018, 144, 740-750.
https://doi.org/10.1016/j.ejmech.2017.12.062

45. Koifman O.I., Ponomarev G.V. A Method of Obtaining Methylpheophorbide, 2013, Patent RF No 2490273.

46. Ponomarev G.V., Koifman O.I. Photosensitizer and Method of its Preparation, 2014, Patent RF No 2523380.

47. Chissov V.I., Skobelkin O.K., Mironov A.F. et.al. Pirogov Russian Journal of Surgery 1994, 12, 3-6.

48. Hayashi T., Hisaeda Y. Acc. Chem. Res. 2002, 35, 35-43.
https://doi.org/10.1021/ar000087t

49. Lindsey J.S. Acc. Chem. Res. 2010, 43, 300-311.
https://doi.org/10.1021/ar900212t

50. Beletskaya I.P., Tyurin V.S., Uglov A., Stern C., Guilard R. Survey of Synthetic Routes for Synthesis and Substitution in Porphyrins. In: Handbook of Porphyrin Science. Vol. 23. (Kadish K.M., Smith K.M., Guilard R., Eds.) World Scientific Publishing, 2012. p. 81-278.
https://doi.org/10.1142/9789814397605_0010

51. Smith K.M. New J. Chem. 2016, 40, 5644-5649.
https://doi.org/10.1039/C6NJ00820H

52. Brückner C. Acc. Chem. Res. 2016, 49, 1080-1092.
https://doi.org/10.1021/acs.accounts.6b00043

53. Smith R.M. Strategies fo the Synthesis of Octaalkylporphyrin Systems. In: The Porphyrin Handbook. Vol. 1. (Kadish K.M., Smith K.M., Guilard R., Eds.) Academic Press: San Diego, 2000. p. 1-43.

54. Lindsey J.S. Synthesis of meso-Substituted Porphyrins. In: The Porphyrin Handbook. Vol. 1. (Kadish K.M., Smith K.M., Guilard R., Eds.) Academic Press: San Diego, 2000. p. 45-118.

55. Semeykin A.S., Syrbu S.A., Koifman O.I. Izv. Vyss. Ucheb. Zav., Ser. Khim. I Khim Technol. 2004, 47, 46-55.

56. Lash T.D. Synthesis of Novel Porphyrinoid Chromophores. In: The Porphyrin Handbook. Vol. 2. (Kadish K.M., Smith K.M., Guilard R., Eds.) Academic Press: San Diego, 2000. p. 125-196.

57. Cheprakov A.V. The Synthesis of π-Extended Porphyrins. In: Handbook of Porphyrin Science Vol. 13. (Kadish K.M., Smith K.M., Guilard R., Eds.) World Scientific Publishing Co. Pte. Ltd.: Singapore, 2011. 1-149.
https://doi.org/10.1142/9789814322386_0010

58. Ishkov Yu.V., Zhilina Z.I., Vodzinskii S.V. In: Advances in Porphyrin Chemistry. Vol. 4. (Golubchikov O.A., Ed.) SPb.: St-PbGU, 2003. p. 31-44.

59. Smith B.E., Lash T.D. Tetrahedron 2010, 66, 4413-442.
https://doi.org/10.1016/j.tet.2010.04.069

60. Hiroto S., Miyake Y., Shinokubo H. Chem. Rev. 2016, 117, 2910-3043.
https://doi.org/10.1021/acs.chemrev.6b00427

61. Tanaka T., Osuka A. Chem. Soc. Rev. 2015, 44, 943-969.
https://doi.org/10.1039/C3CS60443H

62. Koifman O.I., Ageeva T.A. Porphyrin Polymers: Synthesis, Properties, Applications. M.: LENAND, 2018. 304 p.

63. Matano Y. Chem. Rev. 2017, 117, 3138-3191.
https://doi.org/10.1021/acs.chemrev.6b00460

64. Claessens C.G., Hahn U., Torres T. Chem. Rec. 2008, 8, 75-97.
https://doi.org/10.1002/tcr.20139

65. Kobayashi N. Synthesis and Characterization of Chiral Phthalocyanines. In: Handbook of Porphyrin Science. Vol. 23. (Kadish K.M., Smith K.M., Guilard R., Eds.) World Scientific, 2012. p. 373-440.
https://doi.org/10.1142/9789814397605_0012

66. Lomova T.N., Tyulyaeva E.Y., New Trends in the Direct Synthesis of Phthalocyanine/Porphyrin Complexes. In: Direct Synthesis of Metal Complexes. (Kharisov B., Ed.) Elsevier, 2018. p. 239-278.
https://doi.org/10.1016/B978-0-12-811061-4.00006-2

67. Koifman O.I., Ageeva T.A. Russ. Chem. Bull. 2015, 64, 2001-2011.
https://doi.org/10.1007/s11172-016-1111-y

68. Ageeva T.A., Golubev D.V., Gorshkova A.S., Ionov A.M., Koifman O.I., Mozhchil R.N., Rumyantseva V.D., Sigov A.S., Fomichev V.V. Macroheterocycles 2018, 11, 155-161.
https://doi.org/10.6060/mhc180171

69. Ageeva T.A., Golubev D.V., Gorshkova A.S., Ionov A.M., Kohylova E.V., Koifmah O.I., Mozhchil R.N., Rozhkova E.P., Rumyantseva V.D., Sigov A.S., Fomichev V.V. Macroheterocycles 2019, 12, 148-153.
https://doi.org/10.6060/mhc190442f

70. McConnell I., Li G., Brudvi G.W. Chem. Biol. 2010, 17, 434-447.
https://doi.org/10.1016/j.chembiol.2010.05.005

71. Bottari G., Trukhina O., Ince M., Torres T. Coord. Chem. Rev. 2012, 256, 2453-2477.
https://doi.org/10.1016/j.ccr.2012.03.011

72. Drain C.M., Varotto A., Radivojevic I. Chem. Rev. 2009, 109, 1630-1658.
https://doi.org/10.1021/cr8002483

73. Morisue M., Kobuke Y. Supramolecular Organization of Porphyrins and Phthalocyanines by Use of Biomimetic Coordination Methodology. In: Handbook of Porphyrin Science. Vol. 32. (Kadish K.M., Smith K.M., Guilard R., Eds.) World Scientific Publishing, 2014. p. 1-126.
https://doi.org/10.1142/9789814417297_0003

74. Mamardashvili G.M., Mamardashvili N.Zh., Koifman O.I. Russ. Chem. Rev. 2008, 77, 59-75.
https://doi.org/10.1070/RC2008v077n01ABEH003743

75. Koifman O.I., Mamardashvili N.Zh. Nanotechnologies in Russia 2009, 4, 253-261.
https://doi.org/10.1134/S1995078009050012

76. Beletskaya I., Tyurin V.S., Tsivadze A.Y., Guilard R., Stern C. Chem. Rev. 2009, 109, 1659-1713.
https://doi.org/10.1021/cr800247a

77. Koifman O.I., Ageeva T.A. Polymer Sci. Ser. C 2014, 56, 84-103.
https://doi.org/10.1134/S1811238214010056

78. Khelevina O.G., Malyasova A.S., Koifman O.I. Russ. J. Gen. Chem. 2020, 90, 1646-1659.
https://doi.org/10.1134/S1070363220090108

79. Ageeva T.A., Bush A.A., Golubev D.V., Gorshkova A.S., Kamentsev K.E., Koifman O.I., Rumyantseva V.D., Sigov A.S., Fomichev V.V. J. Organomet. Chem. 2020, 922, 121355.
https://doi.org/10.1016/j.jorganchem.2020.121355

80. Percástegui E.G., Jancik V. Coord. Chem. Rev. 2020, 407, 213165.
https://doi.org/10.1016/j.ccr.2019.213165

81. Functional Materials Based on Tetrapyrrole Macroheterocyclic Compounds (Koifman O.I., Ed.) М.: LENAND, 2019. 848 p.

82. Chan K.S., Zhou X., Luo B.S., Mak T.C.W. J. Chem. Soc. Chem. Commun. 1994, 271.
https://doi.org/10.1039/C39940000271

83. Chan K.S., Zhou X.A., Au M.T., Tam C.Y. Tetrahedron 1995, 51, 3129.
https://doi.org/10.1016/0040-4020(95)00069-K

84. Hyslop A.G., Kellett M.A., Iovine P.V., Therien M.J. J. Am. Chem. Soc. 1998, 120, 12676.
https://doi.org/10.1021/ja982410h

85. Ali H., van Lier J.E. Tetrahedron 1994, 50, 11933.
https://doi.org/10.1016/S0040-4020(01)89306-6

86. Shanmugathasan S., Johnson C.K., Edwards C., Matthews E.K., Dolphin D., Boyle R.W. J. Porphyrins Phthalocyanines 2000, 4, 228.
https://doi.org/10.1002/(SICI)1099-1409(200004/05)4:3<228::AID-JPP199>3.3.CO;2-Z

87. Chang J.C., Ma C.J., Lee G.H., Peng S.M., Yeh C.Y. Dalton Trans. 2005, 1504.
https://doi.org/10.1039/B417350C

88. Gauler R., Risch N. Eur. J. Org. Chem. 1998, 1193.
https://doi.org/10.1002/(SICI)1099-0690(199806)1998:6<1193::AID-EJOC1193>3.0.CO;2-K

89. Sergeeva N.N., Scala A., Bakar M.A., O'Riordan G., O'Brien J., Grassi G., Senge M.O. J. Org. Chem. 2009, 74, 7140.
https://doi.org/10.1021/jo901535c

90. Santos F.D., Cunha A.C., de Souza M.C.B.V., Tome A.C., Neves M.G.P.M.S., Ferreira V.F., Cavaleiro J.A.S. Tetrahedron Lett. 2008, 49, 7286.
https://doi.org/10.1016/j.tetlet.2008.10.024

91. Chen Y., Zhang X.P. J. Org. Chem. 2003, 68, 4432.
https://doi.org/10.1021/jo034063m

92. Takanami T., Hayashi M., Hino F., Suda K. Tetrahedron Lett. 2003, 44, 7353.
https://doi.org/10.1016/S0040-4039(03)01837-9

93. Khan M.M., Ali H., van Lier J.E. Tetrahedron Lett. 2001, 42, 1615.
https://doi.org/10.1016/S0040-4039(00)02303-0

94. Gao G.-Y., Chen Y., Zhang X.P. J. Org. Chem. 2003, 68, 6215.
https://doi.org/10.1021/jo034576t

95. Wang K., Osuka A., Song J. ACS Central Science, 2020, 6, 2159-2178.
https://doi.org/10.1021/acscentsci.0c01300

96. Gao G.-Y., Chen Y., Zhang X.P. Org. Lett. 2004, 6, 1837.
https://doi.org/10.1021/ol049440b

97. Gao G.-Y., Ruppel J.V., Allen B., Chen Y., Zhang X.P. J. Org. Chem. 2007, 72, 9060.
https://doi.org/10.1021/jo701476m

98. Artamkina G.A., Sazonov P.K., Shtern M.M., Grishina G.V., Veselov I.S., Semeikin A.S., Syrbu S.A., Koifman O.I., Beletskaya I.P. Synlett 2008, 45-48.
https://doi.org/10.1055/s-2007-992410

99. Artamkina G.A., Sazonov P.K., Shtern M.M., Grishina G.V., Veselov I.S., Semeikin A.S., Syrbu S.A., Koifman O.I., Beletskaya I.P. Russ. J. Org. Chem. 2008, 44, 421.
https://doi.org/10.1134/S1070428008030184

100. Mikhalitsyna E.A., Tyurin V.S., Beletskaya I.P. J. Porphyrins Phthalocyanines 2015, 19, 874.
https://doi.org/10.1142/S1088424615500637

101. Tyurin V.S., Mikhalitsyna E.A., Semeikin A.S., Beletskaya I.P. Macroheterocycles 2015, 8, 358.
https://doi.org/10.6060/mhc150769b

102. Polevaya Y.P., Tyurin V.S., Beletskaya I.P. J. Porphyrins Phthalocyanines 2014, 18, 20.
https://doi.org/10.1142/S1088424613500636

103. Yaschuk Y.P., Tyurin V.S., Beletskaya I.P. Macroheterocycles 2012, 5, 302.
https://doi.org/10.6060/mhc2012.121199b

104. Locos O.B., Arnold D.P. Org. Biomol. Chem. 2006, 4, 902.
https://doi.org/10.1039/b516989e

105. Song J., Jang S.Y., Yamaguchi S., Sankar J., Hiroto S., Aratani N., Shin J.Y., Easwaramoorthi S., Kim K.S., Kim D., Shinokubo H., Osuka T. Angew. Chem. Int. Ed. 2008, 47, 6004.
https://doi.org/10.1002/anie.200802026

106. Mikhalitsyna E.A., Tyurin V.S., Khrustalev V.N., Lonin I.S., Beletskaya I.P. Dalton Trans. 2014, 43, 3563.
https://doi.org/10.1039/c3dt52685b

107. Mikhalitsyna E.A., Tyurin V.S., Zamilatskov I.A., Khrustalev V.N., Beletskaya I.P. Dalton Trans. 2012, 41, 7624.
https://doi.org/10.1039/c2dt30123g

108. Ranyuk E.R., Filatov M.A., Averin A.D., Cheprakov A.V., Beletskaya I.P. Synthesis 2012, 44, 393.
https://doi.org/10.1055/s-0031-1289667

109. Yakushev A.A., Averin A.D., Maloshitskaya O.A., Syrbu S.A., Koifman O.I., Beletskaya I.P. Macroheterocycles 2016, 9, 65.
https://doi.org/10.6060/mhc151206a

110. Yakushev A.A., Averin A.D., Maloshitskaya O.A., Syrbu S.A., Koifman O.I., Beletskaya I.P. Mendeleev Commun. 2016, 26, 199.
https://doi.org/10.1016/j.mencom.2016.04.006

111. Averin A.D., Yakushev A.A., Maloshitskaya O.A., Syrbu S.A., Koifman O.I., Beletskaya I.P. Russ. Chem. Bull. 2017, 66, 1456.
https://doi.org/10.1007/s11172-017-1908-3

112. Yakushev A.A., Averin A.D., Maloshitskaya O.A., Koifman O.I., Syrbu S.A., Beletskaya I.P. Macroheterocycles 2018, 11, 135.
https://doi.org/10.6060/mhc180276a

113. Yakushev A.A., Chernichenko N.M., Anokhin M.V., Averin A.D., Buryak A.K., Denat F., Beletskaya I.P. Molecules 2014, 19, 940.
https://doi.org/10.3390/molecules19010940

114. Yakushev A.A., Averin A.D., Sakovich M.V., Vatsouro I.M., Kovalev V.V., Syrbu S.A., Koifman O.I., Beletskaya I.P. J. Porphyrins Phthalocyanines 2019, 23, 1551.
https://doi.org/10.1142/S1088424619501761

115. Braun A., Tcherniac J. Berichte der Deutschen Chemischen Gesellschaft 1907, 40, 2709-2714.
https://doi.org/10.1002/cber.190704002202

116. Linstead R. P. J. Chem. Soc. (Resumed) 1934, 1016-1017.
https://doi.org/10.1039/jr9340001016

117. Berezin B.D. Coordination Compounds of Porphyrins and Phthalocyanine. New York - Toronto: J. Wiley, 1981. 278 p.

118. Leznoff C.C., Lever A.B.P. In: Phthalocyanines. Properties and Applications (Leznoff C.C., Lever A.B.P., Eds.) New York: VCH, 1989, Vol. 1. 448 p.; 1993, Vol. 2. 305 p.; 1993, Vol. 3. 303 p.; 1996, Vol. 4. 536 p.

119. Allen C.M., Sharman W.M., Van Lier J.E. J. Porphyrins Phthalocyanines 2001, 5, 161-169.
https://doi.org/10.1002/jpp.324

120. Walter M.G., Rudine A.B., Wamser C.C. J. Porphyrins Phthalocyanines 2010, 14, 759-792.
https://doi.org/10.1142/S1088424610002689

121. Wang H., Qi D., Xie Z., Cao W., Wang K., Shang H., Jiang J. Chem. Commun. 2013, 49, 889-891.
https://doi.org/10.1039/C2CC38088A

122. Fukuda T., Biyajima T., Kobayashi N. J. Am. Chem. Soc. 2010, 132, 6278-6279.
https://doi.org/10.1021/ja100125e

123. Horii Y., Horie Y., Katoh K., Breedlove B.K., Yamashita M. Inorg. Chem., 2018, 57, 565-574.
https://doi.org/10.1021/acs.inorgchem.7b02124

124. Wang H., Kobayashi N., Jiang J. Chem. Eur. J. 2012, 18, 1047-1049.
https://doi.org/10.1002/chem.201103037

125. Korostei Y.S., Tarasova V.G., Pushkarev V.E., Borisova N.E., Vorobiev A.K., Tomilova L.G. Dyes and Pigments 2018, 159, 573-575.
https://doi.org/10.1016/j.dyepig.2018.07.030

126. Korostei Y.S., Pushkarev V.E., Tolbin A.Y., Dzuban A.V., Chernyak A.V., Konev D.V., Medvedeva T.O., Talantsev A.D., Sanina N.A., Tomilova L.G. Dyes and Pigments 2019, 170, 107648.
https://doi.org/10.1016/j.dyepig.2019.107648

127. Chen Y., Liu C., Ma F., Qi D., Liu Q., Sun H.-L., Jiang J. Chem. Eur. J. 2018, 24, 8066-8070.
https://doi.org/10.1002/chem.201800408

128. Pushkarev V.E., Tolbin A.Y., Zhurkin F.E., Borisova N.E., Trashin S.A., Tomilova L.G., Zefirov N.S. Chem. Eur. J. 2012, 18, 9046-9055.
https://doi.org/10.1002/chem.201200361

129. Korostei Y.S., Tolbin A.Y., Dzuban A.V., Pushkarev V.E., Sedova M.V., Maklakov S.S., Tomilova L.G. Dyes and Pigments 2018, 149, 201-211.
https://doi.org/10.1016/j.dyepig.2017.09.066

130. Wang K., Qi D., Wang H., Cao W., Li W., Jiang J. Chem. Eur. J. 2012, 18, 15948-15952.
https://doi.org/10.1002/chem.201202888

131. Balashova I.O., Pushkarev V.E., Shestov V.I., Tomilova L.G., Koifman O.I., Ponomarev G.V. Macroheterocycles 2015, 8, 233-238.
https://doi.org/10.6060/mhc150767p

132. Tomilova L.G., Pushkarev V.E., Balashova I.O., Shestov V.I., Ponomarev G.V., Koifman O.I., Platonova Y.B., Volov A.N. 2020, Patent RF No 2722309.

133. Quartarolo A.D., Pérusse D., Dumoulin F., Russo N., Sicilia E. J. Porphyrins Phthalocyanines 2013, 17, 980-988.
https://doi.org/10.1142/S1088424613500569

134. Yang K., Wang J., Zhao Z., Zhao F., Wang K., Zhang X., Zhang F. Org. Electron. 2020, 83, 105739.
https://doi.org/10.1016/j.orgel.2020.105739

135. Li W., Liu W., Zhang X., Yan D., Liu F., Zhan C. Macromol. Rapid Commun. 2019, 40, 1900353.
https://doi.org/10.1002/marc.201900353

136. Kobayashi N., Furuyama T., Satoh K. J. Am. Chem. Soc. 2011, 133, 19642-19645.
https://doi.org/10.1021/ja208481q

137. Lukyanets E.A., Nemykin V.N. J. Porphyrins Phthalocyanines 2010, 14, 1-40.
https://doi.org/10.1142/S1088424610001799

138. Kobayashi N., Nakajima S.-I., Ogata H., Fukuda T. Chem. Eur. J. 2004, 10, 6294-6312.
https://doi.org/10.1002/chem.200400275

139. Muranaka A., Yonehara M., Uchiyama M. J. Am. Chem. Soc. 2010, 132, 7844-7845.
https://doi.org/10.1021/ja101818g

140. Ince M., Hausmann A., Martínez-Díaz M.V., Guldi D.M., Torres T. Chem. Commun. 2012, 48, 4058-4060.
https://doi.org/10.1039/c2cc30632h

141. Dubinina T.V., Tomilova L.G., Zefirov N.S. Russ. Chem. Rev. 2013, 82, 865-895.
https://doi.org/10.1070/RC2013v082n09ABEH004353

142. Dubinina T.V., Trashin S.A., Borisova N.E., Boginskaya I.A., Tomilova L.G., Zefirov N.S. Dyes and Pigments 2012, 93, 1471-1480.
https://doi.org/10.1016/j.dyepig.2011.10.012

143. Makarov S.G., Suvorova O.N., Litwinski C., Ermilov E.A., Röder B., Tsaryova O., Dülcks T., Wöhrle D. Eur. J. Inorg. Chem. 2007, 2007, 546-552.
https://doi.org/10.1002/ejic.200600843

144. Dubinina T.V., Ivanov A.V., Borisova N.E., Trashin S.A., Gurskiy S.I., Tomilova L.G., Zefirov N.S. Inorg. Chim. Acta 2010, 363, 1869-1878.
https://doi.org/10.1016/j.ica.2010.02.011

145. Dubinina T.V., Paramonova K.V., Trashin S.A., Borisova N.E., Tomilova L.G., Zefirov N.S. Dalton Trans. 2014, 43, 2799-2809.
https://doi.org/10.1039/C3DT52726C

146. Dubinina T.V., Pushkarev V.E., Trashin S., Paramonova K.V., Tomilova L.G. Macroheterocycles 2012, 5, 366-370.
https://doi.org/10.6060/mhc2012.121213d

147. Berendonk T.U., Manaia C.M., Merlin C., Fatta-Kassinos D., Cytryn E., Walsh F., Bürgmann H., Sørum H., Norström M., Pons M.-N., Kreuzinger N., Huovinen P., Stefani S., Schwartz T., Kisand V., Baquero F., Martinez J.L. Nat. Rev. Microbiology 2015, 13, 310-317.
https://doi.org/10.1038/nrmicro3439

148. Cizmas L., Sharma V.K., Gray C.M., McDonald T.J. Environ. Chem. Lett. 2015, 13, 381-394.
https://doi.org/10.1007/s10311-015-0524-4

149. Larsson D.G.J. Upsala J. Med. Sci. 2014, 119, 108-112.
https://doi.org/10.3109/03009734.2014.896438

150. EU Action on Antimicrobial Resistance, https://ec.europa.eu/health/antimicrobial-resistance/eu-action-on-antimicrobial-resistance_en (date of access 20.11.2020).

151. WHO multi-country survey reveals widespread public misunderstanding about antibiotic resistance, https://www.who.int/en/news-room/detail/16-11-2015-who-multi-country-survey-reveals-widespread-public-misunderstanding-about-antibiotic-resistance (date of access 20.11.2020).

152. Unceta N., Sampedro M.C., Bakar N.K.A., Gómez-Caballero A., Goicolea M.A., Barrio R.J. J. Chromatogr. A 2010, 1217, 3392-3399.
https://doi.org/10.1016/j.chroma.2010.03.008

153. Berna M.J., Ackermann B.L., Murphy A.T. Anal. Chim. Acta 2004, 509, 1-9.
https://doi.org/10.1016/j.aca.2003.12.023

154. Ferrer I., Zweigenbaum J.A., Thurman E.M. J. Chromatogr. A 2010, 1217, 5674-5686.
https://doi.org/10.1016/j.chroma.2010.07.002

155. Feier B., Gui A., Cristea C., Săndulescu R. Anal. Chim. Acta 2017, 976, 25-34.
https://doi.org/10.1016/j.aca.2017.04.050

156. Cristea C., Florea A., Tertiș M., Săndulescu R. Immunosensors. In: Biosensors - Micro and Nanoscale Applications (Rinken T., Ed.). IntechOpen, 2015.
https://doi.org/10.5772/60524

157. Trashin S., Rahemi V., Ramji K., Neven L., Gorun S.M., De Wael K. Nat. Commun. 2017, 8, 16108.
https://doi.org/10.1038/ncomms16108

158. Khan S.U., Trashin S.A., Korostei Y.S., Dubinina T.V., Tomilova L.G., Verbruggen S.W., De Wael K., ChemPhotoChem 2020, 4, 300-306.
https://doi.org/10.1002/cptc.201900275

159. Merkel P.B., Kearns D.R. J. Am. Chem. Soc. 1972, 94, 7244-7253.
https://doi.org/10.1021/ja00776a003

160. Davies M.J. Methods 2016, 109, 21-30.
https://doi.org/10.1016/j.ymeth.2016.05.013

161. Valduga G., Nonell S., Reddi E., Jori G., Braslavsky S.E. Photochem. Photobiol. 1988, 48, 1-5.
https://doi.org/10.1111/j.1751-1097.1988.tb02778.x

162. Tanielian C., Wolff C., Esch M. J. Phys. Chem. 1996, 100, 6555-6560.
https://doi.org/10.1021/jp952107s

163. del Rey B., Keller U., Torres T., Rojo G., Agullo-Lopez F., Nonell S., Marti C., Brasselet S., Ledoux I., Zyss J. J. Am. Chem. Soc. 1998, 120, 12808-12817.
https://doi.org/10.1021/ja980508q

164. Dubinina T.V., Osipova M.M., Zasedatelev A.V., Krasovskii V.I., Borisova N.E., Trashin S.A., Tomilova L.G., Zefirov N.S. Dyes and Pigments 2016, 128, 141-148.
https://doi.org/10.1016/j.dyepig.2016.01.023

165. Wilkinson F., Helman W.P., Ross A.B. J. Phys. Chem. Ref. Data 1993, 22, 113-262.
https://doi.org/10.1063/1.555934

166. Potz R., Goeldner M., Hueckstaedt H., Cornelissen U., Tutass A., Homborg H. ChemInform 2000, 31 (16).
https://doi.org/10.1002/chin.200016159

167. Nyokong T. Coord. Chem. Rev. 2007, 251, 1707-1722.
https://doi.org/10.1016/j.ccr.2006.11.011

168. Burtsev I.D., Dubinina T.V., Platonova Y.B., Kosov A.D., Pankratov D.A., Tomilova L.G. Mendeleev Commun. 2017, 27, 466-469.
https://doi.org/10.1016/j.mencom.2017.09.012

169. Platonova Y.B., Morozov A.S., Burtsev I.D., Korostei Y.S., Ionidi V.Y., Romanovsky B.V., Tomilova L.G. Mendeleev Commun. 2018, 28, 198-199.
https://doi.org/10.1016/j.mencom.2018.03.030

170. Burtsev I.D., Platonova Y.B., Volov A.N., Tomilova L.G. Polyhedron 2020, 188, 114697.
https://doi.org/10.1016/j.poly.2020.114697

171. Moiseeva E.O., Platonova Y.B., Konev D.V., Trashin S.A., Tomilova L.G. Mendeleev Commun. 2019, 29, 212-214.
https://doi.org/10.1016/j.mencom.2019.03.033

172. Novikov R.A., Levina A.A., Borisov D.D., Volodin A.D., Korlyukov A.A., Tkachev Y.V., Platonova Y.B., Tomilova L.G., Tomilov Y.V. Organometallics 2020, 39, 2580-2593.
https://doi.org/10.1021/acs.organomet.0c00113

173. Burtsev I.D., Platonova Y.B., Volov A.N., Tomilova L.G. Macroheterocycles 2020, 13, 126-129.
https://doi.org/10.6060/mhc200286t

174. Platonova Y.B., Volov A.N., Tomilova L.G. J. Catalysis 2019, 373, 222-227.
https://doi.org/10.1016/j.jcat.2019.04.003

175. Platonova Y.B., Volov A.N., Tomilova L.G. Bioorg. Med. Chem. Lett. 2020, 30, 127351.
https://doi.org/10.1016/j.bmcl.2020.127351

176. Platonova Y.B., Volov A.N., Tomilova L.G. J. Catalysis 2020, 391, 224-228.
https://doi.org/10.1016/j.jcat.2020.08.019

177. Leyzerovich N.N., Shvedene N.V., Blikova Y.N., Tomilova L.G., Pletnev I.V. Electroanalysis 2001, 13, 246-252.
https://doi.org/10.1002/1521-4109(200103)13:3<246::AID-ELAN246>3.0.CO;2-7

178. Shvedene N.V., Otkidach K.N., Gumerov M.R., Tarakanov P.A., Tomilova L.G. J. Anal. Chem. 2015, 70, 72-80.
https://doi.org/10.1134/S1061934815010177

179. Blikova Y.N., Ivanov A.V., Tomilova L.G., Shvedene N.V. Russ. Chem. Bull. 2003, 52, 150-153.
https://doi.org/10.1023/A:1022456601080

180. Shvedene N.V., Abashev M.N., Arakelyan S.A., Otkidach K.N., Tomilova L.G., Pletnev I.V. J. Solid State Electrochem. 2019, 23, 543-552.
https://doi.org/10.1007/s10008-018-4159-9

181. Tolbin A.Y., Tomilova L.G. Russ. Chem. Rev. 2011, 80, 531-551.
https://doi.org/10.1070/RC2011v080n06ABEH004198

182. Shvedene N.V., Otkidach K.N., Ondar E.E., Osipova M.M., Dubinina T.V., Tomilova L.G., Pletnev I.V. J. Anal. Chem. 2017, 72, 95-104.
https://doi.org/10.1134/S1061934817010117

183. Sheik-Bahae M., Said A.A., Wei T., Hagan D.J., Stryland E.W.V. IEEE J. Quantum Electronics 1990, 26, 760-769.
https://doi.org/10.1109/3.53394

184. Oluwole D.O., Ngxeke S.M., Britton J., Nyokong T. J. Photochem. Photobiol., A: Chemistry 2017, 347, 146-159.
https://doi.org/10.1016/j.jphotochem.2017.07.032

185. Sekhosana K.E., Amuhaya E., Nyokong T. Polyhedron 2016, 105, 159-169.
https://doi.org/10.1016/j.poly.2015.12.045

186. Mgidlana S., Şen P., Nyokong T. J. Mol. Struct. 2020, 1220, 128729.
https://doi.org/10.1016/j.molstruc.2020.128729

187. Bankole O.M., Osifeko O., Nyokong T. J. Photochem. Photobiol., A: Chemistry 2016, 329, 155-166.
https://doi.org/10.1016/j.jphotochem.2016.06.025

188. Kuzmina E.A., Dubinina T.V., Borisova N.E., Tarasevich B.N., Krasovskii V.I., Feofanov I., Dzuban A.V., Tomilova L.G. Dyes and Pigments 2020, 174, 108075.
https://doi.org/10.1016/j.dyepig.2019.108075

189. Kuzmina E.A., Dubinina T.V., Zasedatelev A.V., Baranikov A.V., Makedonskaya M.I., Egorova T.B., Tomilova L.G. Polyhedron 2017, 135, 41-48.
https://doi.org/10.1016/j.poly.2017.06.048

190. Kuzmina E.A., Dubinina T.V., Dzuban A.V., Krasovskii V.I., Maloshitskaya O.A., Tomilova L.G. Polyhedron 2018, 156, 14-18.
https://doi.org/10.1016/j.poly.2018.08.076

191. Pan F., Gao S., Chen C., Song C., Zeng F. Mater. Sci. Eng.: R: Reports 2014, 83, 1-59.
https://doi.org/10.1016/j.mser.2014.06.002

192. Chen Y., Song H., Jiang H., Li Z., Zhang Z., Sun X., Li D., Miao G. Appl. Phys. Lett. 2014, 105, 193502.
https://doi.org/10.1063/1.4901747

193. Tseng R.J., Huang J., Ouyang J., Kaner R.B., Yang Nano Lett. 2005, 5, 1077-1080.
https://doi.org/10.1021/nl050587l

194. Kotova M.S., Drozdov K.A., Dubinina T.V., Kuzmina E.A., Tomilova L.G., Vasiliev R.B., Dudnik A.O., Ryabova L.I., Khokhlov D.R. Scientific Reports 2018, 8, 9080.
https://doi.org/10.1038/s41598-018-27332-1

195. Gonzalez-Anton R., Osipova M.M., Garcia-Hernandez C., Dubinina T.V., Tomilova L.G., Garcia-Cabezon C., Rodriguez-Mendez M.L. Electrochimica Acta 2017, 255, 239-247.
https://doi.org/10.1016/j.electacta.2017.09.168

196. Martynov A.G., Safonova E.A., Tsivadze A.Y., Gorbunova Y.G. Coord. Chem. Rev. 2019, 387, 325-347.
https://doi.org/10.1016/j.ccr.2019.02.004

197. Yamashita M. Bull. Chem. Soc. Jpn. 2020, bcsj.20200257.

198. Sessoli R., Gatteschi D., Caneschi A., Novak M.A. Nature 1993, 365, 141-143.
https://doi.org/10.1038/365141a0

199. Ishikawa N., Sugita M., Ishikawa T., Koshihara S.-Y., Kaizu Y. J. Am. Chem. Soc. 2003, 125, 8694-8695.
https://doi.org/10.1021/ja029629n

200. Ishikawa N., Sugita M., Ishikawa T., Koshihara S., Kaizu Y. J. Phys. Chem. B 2004, 108, 11265-11271.
https://doi.org/10.1021/jp0376065

201. Wang H., Wang B.W., Bian Y., Gao S., Jiang J. Coord. Chem. Rev. 2016, 306, 195-216.
https://doi.org/10.1016/j.ccr.2015.07.004

202. Ishikawa N., Iino T., Kaizu Y. J. Am. Chem. Soc. 2002, 124, 11440-11447.
https://doi.org/10.1021/ja027119n

203. Ishikawa N., Otsuka S., Kaizu Y. Angew. Chem. Int. Ed. 2005, 44, 731-3.
https://doi.org/10.1002/anie.200461546

204. Holmberg R.J., Polovkova M.A., Martynov A.G., Gorbunova Y.G., Murugesu M. Dalton Trans. 2016, 45, 9320-9327.
https://doi.org/10.1039/C6DT00777E

205. Lan Y., Klyatskaya S., Ruben M., Fuhr O., Wernsdorfer W., Candini A., Corradini V., Lodi Rizzini A., del Pennino U., Troiani F., Joly L., Klar D., Wende H., Affronte M. J. Mater. Chem., C 2015, 3, 9794-9801.
https://doi.org/10.1039/C5TC02011E

206. Polovkova M.A., Martynov A.G., Birin K.P., Nefedov S.E., Gorbunova Y.G., Tsivadze A.Y. Inorg. Chem. 2016, 55, 9258-9269.
https://doi.org/10.1021/acs.inorgchem.6b01292

207. Sakaue S., Fuyuhiro A., Fukuda T., Ishikawa N. Chem. Commun. 2012, 48, 5337.
https://doi.org/10.1039/c2cc31125a

208. Katoh K., Breedlove B.K., Yamashita M. Chem. Sci. 2016, 7, 4329-4340.
https://doi.org/10.1039/C5SC04669F

209. Sugimoto H., Higashi T., Maeda A., Mori M., Masuda H., Taga T. J. Chem. Soc., Chem. Commun. 1983, 1234-1235.
https://doi.org/10.1039/C39830001234

210. Maeda A., Sugimoto H. J. Chem. Soc. Faraday Trans. 2 1986, 82, 2019.
https://doi.org/10.1039/f29868202019

211. Ge J., Qiu Y., Wang H., Su J., Wang P., Chen Z. Chem. - An Asian J. 2020, 15, 3013-3019.
https://doi.org/10.1002/asia.202000655

212. Ge J.-Y., Wang H.-Y., Li J., Xie J.-Z., Song Y., Zuo J.-L. Dalton Trans. 2017, 46, 3353-3362.
https://doi.org/10.1039/C7DT00298J

213. Fukuda T., Kuroda W., Ishikawa N. Chem. Commun. 2011, 47, 11686.
https://doi.org/10.1039/c1cc14657b

214. Katoh K., Horii Y., Yasuda N., Wernsdorfer W., Toriumi K., Breedlove B.K., Yamashita M. Dalton Trans. 2012, 41, 13582-13600.
https://doi.org/10.1039/c2dt31400b

215. Horii Y., Katoh K., Sugimoto K., Nakanishi R., Breedlove B.K., Yamashita M. Chem. Eur. J. 2019, 3098-3104.
https://doi.org/10.1002/chem.201805368

216. Morita T., Damjanović M., Katoh K., Kitagawa Y., Yasuda N., Lan Y., Wernsdorfer W., Breedlove B.K., Enders M., Yamashita M. J. Am. Chem. Soc. 2018, 140, 2995-3007.
https://doi.org/10.1021/jacs.7b12667

217. Tolbin A.Y., Pushkarev V.E., Shulishov E.V., Tomilova L.G. J. Porphyrins Phthalocyanines 2012, 16, 341-350.
https://doi.org/10.1142/S108842461250037X

218. Horii Y., Katoh K., Breedlove B.K., Yamashita M. Chem. Commun. 2017, 53, 8561-8564.
https://doi.org/10.1039/C7CC03553E

219. Horii Y., Kishiue S., Damjanović M., Katoh K., Breedlove B.K., Enders M., Yamashita M. Chem. Eur. J. 2018, 24, 4320-4327.
https://doi.org/10.1002/chem.201705378

220. Martynov A.G., Polovkova M.A., Berezhnoy G.S., Sinelshchikova A.A., Dolgushin F.M., Birin K.P., Kirakosyan G.A., Gorbunova Y. G., Tsivadze A.Y. Inorg. Chem. 2020, 59, 9424-9433.
https://doi.org/10.1021/acs.inorgchem.0c01346

221. Martynov A.G., Gorbunova Y.G. Polyhedron 2010, 29, 391-399.
https://doi.org/10.1016/j.poly.2009.06.009

222. Martynov A.G., Gorbunova Y.G., Tsivadze A.Y. Dalton Trans. 2011, 40, 7165-7171.
https://doi.org/10.1039/c1dt10455a

223. Birin K.P., Gorbunova Y.G., Tsivadze A.Y. Magn. Reson. Chem. 2010, 48, 505-515.
https://doi.org/10.1002/mrc.2612

224. Gorbunova Y.G., Martynov A.G., Birin K.P., Tsivadze A.Y. Russ. J. Inorg. Chem. 2021, in press.

225. Wöhrle D., Schnurpfeil G., Makarov S.G., Kazarin A., Suvorova O.N. Macroheterocycles 2012, 5, 191-202.
https://doi.org/10.6060/mhc2012.120990w

226. The Porphyrin Handbook. Vol. 1-14. (Kadish K.M., Smith K.M., Guilard R., Eds.) San Diego: Academic Press, 2010.

227. Inabe T., Tajima H. Chem. Rev. 2004, 104, 5503-5534.
https://doi.org/10.1021/cr030649x

228. Yu D.E.C., Matsuda M., Tajima H., Kikuchi A., Taketsugu T., Hanasaki N., Naito T., Inabe T. J. Mater. Chem. 2009, 19, 718-723.
https://doi.org/10.1039/B814609H

229. Konarev D.V., Kuzmin A.V., Simonov S.V., Khasanov S.S., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Dalton Trans. 2012, 41, 13841-13847.
https://doi.org/10.1039/c2dt31587d

230. Konarev D.V., Khasanov S.S., Ishikawa M., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Inorg. Chem. 2013, 52, 3851-3859.
https://doi.org/10.1021/ic3025364

231. Konarev D.V., Zorina L.V., Khasanov S.S., Hakimova E.U., Lyubovskaya R.N. New J. Chem. 2012, 36, 48-51.
https://doi.org/10.1039/C1NJ20858F

232. Konarev D.V., Kuzmin A.V., Faraonov M.A., Ishikawa M., Nakano Y., Khasanov S.S., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Chem. Eur. J. 2015, 21, 1014-1028.
https://doi.org/10.1002/chem.201404925

233. Konarev D.V., Faraonov M.A., Kuzmin A.V., Khasanov S.S., Nakano Y., Batov M.S., Norko S.I., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. New J. Chem. 2017, 41, 6866-6874.
https://doi.org/10.1039/C7NJ00530J

234. Konarev D.V., Khasanov S.S., Kuzmin A.V., Nakano Y., Ishikawa M., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Cryst. Growth Des. 2017, 17, 753-762.
https://doi.org/10.1021/acs.cgd.6b01612

235. Konarev D.V., Kuzmin A.V., Khasanov S.S., Batov M.S., Otsuka A., Yamochi H., Kitagawa H., Lyubovskaya R.N. CrystEngComm 2018, 20, 385-401.
https://doi.org/10.1039/C7CE01918A

236. Konarev D.V., Kuzmin A.V., Batov M.S., Khasanov S.S., Otsuka A., Yamochi H., Kitagawa H., Lyubovskaya R.N. ACS Omega 2018, 3, 14875-14888.
https://doi.org/10.1021/acsomega.8b02221

237. Konarev D.V., Kuzmin A.V., Nakano Y., Faraonov M.A., Khasanov S.S., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Inorg. Chem. 2016, 55, 1390-1402.
https://doi.org/10.1021/acs.inorgchem.5b01906

238. Konarev D.V., Kuzmin A.V., Fatalov A.M., Khasanov S.S., Yudanova E.I., Lyubovskaya R.N. Chem. Eur. J. 2018, 24, 8415-8423.
https://doi.org/10.1002/chem.201800873

239. Konarev D.V., Zorina L.V., Khasanov S.S., Shestakov A.F., Fatalov A.M., Otsuka A., Yamochi H., Kitagawa H., Lyubovskaya R.N. Inorg. Chem. 2018, 57, 583-589.
https://doi.org/10.1021/acs.inorgchem.7b02351

240. Konarev D.V., Kuzmin A.V., Shestakov A.F., Khasanov S.S., Lyubovskaya R.N. Dalton Trans. 2019, 48, 4961-4972.
https://doi.org/10.1039/C9DT00655A

241. Konarev D.V., Kuzmin A.V., Khasanov S.S., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Eur. J. Inorg. Chem. 2016, 4099-4103.
https://doi.org/10.1002/ejic.201600680

242. Konarev D.V., Kuzmin A.V., Nakano Y., Khasanov S.S., Otsuka A., Yamochi H., Kitagawa H., Lyubovskaya R.N. Dalton Trans. 2018, 47, 4661-4671.
https://doi.org/10.1039/C8DT00459E

243. Konarev D.V., Kuzmin A.V., Khasanov S.S., Otsuka A., Yamochi H., Kitagawa H., Lyubovskaya R.N. Inorg. Chim. Acta 2020, 510, 119732.
https://doi.org/10.1016/j.ica.2020.119732

244. Konarev D.V., Troyanov S.I., Kuzmin A.V., Nakano Y., Khasanov S.S., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Organometallics 2015, 34, 879-889.
https://doi.org/10.1021/om501210s

245. Kubiak R., Janczak J. J. Alloys Compd. 1992, 189, 107-111.
https://doi.org/10.1016/0925-8388(92)90054-D

246. Janczak J., Kubiak R. Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 2003, 59, m237-m240.
https://doi.org/10.1107/S0108270103009417

247. Janczak J., Kubiak R., Śledź M., Borrmann H., Grin Y. Polyhedron 2003, 22, 2689-2697.
https://doi.org/10.1016/S0277-5387(03)00361-9

248. Janczak J., Kubiak R. Inorg. Chim. Acta 2003, 342, 64-76.
https://doi.org/10.1016/S0020-1693(02)01060-5

249. Konarev D.V., Khasanov S.S., Ishikawa M., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Chem. Asian J. 2017, 12, 910-919.
https://doi.org/10.1002/asia.201700138

250. Zhou W., Thompson J.R., Leznoff C.C., Lez D.B. Chem. Eur. J. 2017, 23, 2323-2331.
https://doi.org/10.1002/chem.201604155

251. Hiroto S., Furukawa K., Shinokubo H., Osuka A. J. Am. Chem. Soc. 2006, 128, 12380-12381.
https://doi.org/10.1021/ja062654z

252. Wong E.W.Y., Leznoff D.B. J. Porphyrins Phthalocyanines 2012, 16, 154-162.
https://doi.org/10.1142/S1088424611004440

253. Konarev D.V., Zorina L.V., Khasanov S.S., Lyubovskaya R.N. Dalton Trans. 2012, 41, 9170-9175.
https://doi.org/10.1039/C1DT11040C

254. Konarev D.V., Karimov D.R., Khasanov S.S., Shestakov A.F., Otsuka A., Yamochi H., Kitagawa H., Lyubovskaya R.N. Dalton. Trans. 2017, 46, 13994-14001.
https://doi.org/10.1039/C7DT02901B

255. Konarev D.V., Khasanov S.S., Kumin A.V., Nakano Y., Ishikawa M., Otsuka A., Yamochi H., Saito G., Lyubovskaya R.N. Inorg. Chem. 2017, 56, 1804-1813.
https://doi.org/10.1021/acs.inorgchem.6b01932

256. Kitagawa T., Lee Y., Takeuchi K. Chem. Commun. 1999, 1529-1530.
https://doi.org/10.1039/a903911b

257. Ishikawa N. Phthalocyanine-based Magnets. In: Functional Phthalocyanine Molecular Materials. Vol. 135. (Jiang J., Ed.) Berlin: Struct. Bonding, 2010. p. 211-228.
https://doi.org/10.1007/978-3-642-04752-7_7

258. Barraclough C.G., Martin R.L., Mitra S., Sherwood R.C. J. Chem. Phys. 1970, 53, 1638-1642.
https://doi.org/10.1063/1.1674236

259. Barraclough C.G., Gregson A.K., Mitra S. J. Chem. Phys. 1974, 60, 962-968.
https://doi.org/10.1063/1.1681174

260. Mitra S., Gregson A.K., Hatfield W., Weller R. Inorg. Chem. 1983, 22, 1729-1732.
https://doi.org/10.1021/ic00154a007

261. Evangelisti M., Bartolome J., de Jongh L.J., Filoti G. Phys. Rev. B 2002, 66, 144410.
https://doi.org/10.1103/PhysRevB.66.144410

262. Korepanov V.I., Sedlovets D.M. Macroheterocycles 2019, 12, 232-243.
https://doi.org/10.6060/mhc190864s

263. Giménez-Agulló N., de Pipaón C.S., Adriaenssens L., Filibian M., Martínez-Belmonte M., Escudero-Adán E.C., Carretta P., Ballester P., Galán-Mascarós J.R. Chem. Eur. J. 2014, 20, 12817-12825.
https://doi.org/10.1002/chem.201402869

264. Zhang P., Guo Y.-N., Tang J. Coord. Chem. Rev. 2013, 257, 1728-1763.
https://doi.org/10.1016/j.ccr.2013.01.012

265. Magnani N. Int. J. Quantum Chemistry 2014, 114, 755-759.
https://doi.org/10.1002/qua.24656

266. Kan J., Wang H., Sun W., Cao W., Tao J., Jiang J. Inorg. Chem. 2013, 52, 8505-8510.
https://doi.org/10.1021/ic400485y

267. Wang K., Zeng S., Wang H., Dou J., Jiang J. Inorg. Chem. Front. 2014, 1, 167-171.
https://doi.org/10.1039/c3qi00097d

268. Lomova T.N. Axially Coordinated Metalloporphyrins in Science and Application. Moscow: URSS, 2018. 700 p.

269. Beltran-Lopez J.F., Sazatornil M., Palacios E., Burriel R. J. Therm. Anal. Calorim. 2016, 125, 579-583.
https://doi.org/10.1007/s10973-016-5268-2

270. Liu J.-L., Chen Y.-C., Guo F.-S., Tong M.-L. Coord. Chem. Rev. 2014, 281, 26-49.
https://doi.org/10.1016/j.ccr.2014.08.013

271. Ishikawa N., Sugita M., Wernsdorfer W. Angew. Chem. Int. Ed. 2005, 44, 2931-2935.
https://doi.org/10.1002/anie.200462638

272. Sharples J.W., Collison D. Polyhedron SI 2013, 66, 15-27.
https://doi.org/10.1016/j.poly.2013.08.005

273. Korolev V.V., Korolev D.V., Lomova T.N., Mozhzhukhina E.G., Zakharov A.G. Russ. J. Phys. Chem. A 2012, 86, 504-508.
https://doi.org/10.1134/S0036024412030181

274. Korolev V.V., Romanov A.S., Arefyev I.M. Russ. J. Phys. Chem. A 2006, 80, 464-466.
https://doi.org/10.1134/S0036024406030277

275. Korolev V.V., Korolev D.V., Ramazanova A.G. J. Therm. Anal. Calorim. 2019, 136, 937-941.
https://doi.org/10.1007/s10973-018-7704-y

276. Korolev V.V., Klyueva M.E., Arefyev I.M., Ramazanova A.G., Lomova T.N., Zakharov A.G. Macroheterocycles 2008, 1, 68-71.
https://doi.org/10.6060/mhc2008.1.68

277. Klyueva M.E., Korolev V.V., Arefyev I.M., Lomova T.N. J. Porphyrins Phthalocyanines 2008, 12, 584.

278. Korolev V.V., Aref'ev I.M., Lomova T.N., Klyueva M.E., Zakharov A.G., Korolev D.V. Russ. J. Phys. Chem. A 2010, 84, 1631-1635.
https://doi.org/10.1134/S0036024410090335

279. Korolev V.V., Aref'ev I.M., Lomova T.N., Ovchenkova E.N., Klyueva M.E., Zakharov A.G., Korolev D.V. Russ. J. Phys. Chem. A 2012, 86, 1165-1170.
https://doi.org/10.1134/S0036024412070102

280. Lomova T.N., Korolev V.V., Ramazanova A.G., Ovchenkova E.N. J. Porphyrins Phthalocyanines 2015, 19, 1262-1269.
https://doi.org/10.1142/S1088424615501114

281. Korolev V.V., Lomova T.N., Ramazanova A.G., Mozhzhukhina E.G. Synth. Met. 2016, 220, 502-507.
https://doi.org/10.1016/j.synthmet.2016.07.026

282. Korolev V.V., Lomova T.N., Ramazanova A.G., Mozhzhukhina E.G. Mend. Commun. 2016, 26, 301-303.
https://doi.org/10.1016/j.mencom.2016.07.011

283. Korolev V.V., Lomova T.N., Ramazanova A.G., Korolev D.V., Mozhzhukhina E.G. J. Organomet. Chem. 2016, 819, 209-215.
https://doi.org/10.1016/j.jorganchem.2016.07.002

284. Lomova T.N., Korolev V.V., Bichan N.G., Ovchenkova E.N., Ramazanova A.G., Balmasova O.V., Gruzdev M.S. Synth. Met. 2019, 253, 116-121.
https://doi.org/10.1016/j.synthmet.2019.05.004

285. Korolev V.V., Lomova T.N., Ramazanova A.G. Radioelektr. Nanosistem. Inform. Tekhnol. [Radio Electronics. Nanosystems. Information Technology] 2019, 11, 199-216 (in Russ.).

286. Korolev V.V., Lomova T.N., Maslennikova A.N., Korolev D.V., Shpakovsky D.B., Zhang J., Milaeva E.R. J. Magn. Magn. Mater. 2016, 401, 86-90.
https://doi.org/10.1016/j.jmmm.2015.10.014

287. Miller J.S., Calabrese J.C., McLean R.S., Epstein A.J. Adv. Mater. 1992, 4, 498-501.
https://doi.org/10.1002/adma.19920040710

288. Miller J.S., Vazquez C., Calabrese J.C., McLean R.S., Epstein A.J. Adv. Mater. 1994, 6, 217-221.
https://doi.org/10.1002/adma.19940060306

289. Böhm A., Vazquez C., McLean R.S., Calabrese J.C., Kalm S.E., Manson J.L., Epstein A.J., Miller J.S. Inorg. Chem. 1996, 35, 3083-3088.
https://doi.org/10.1021/ic9516267

290. Brandon E.J., Arif A.M., Burkhart B.M., Miller J.S. Inorg. Chem. 1998, 37, 2792-2798.
https://doi.org/10.1021/ic9710768

291. Zhang Y.J. Alloys and Compounds 2019, 787, 1173-1186.
https://doi.org/10.1016/j.jallcom.2019.02.175

292. Ovchenkova E.N., Bichan N.G., Tsaturyan A.A., Kudryakova N.O., Gruzdev M.S., Gostev F.E., Shelaev I.V., Nadtochenko V.A., Lomova T.N. J. Phys. Chem. C 2020, 124, 4010-4023.
https://doi.org/10.1021/acs.jpcc.9b11661

293. Andreenko A.S., Belov K.P., Nikitin S.A. Uspehi fizicheskih nauk 1989, 158, 553-579. (in Russ.).
https://doi.org/10.3367/UFNr.0158.198908a.0553

294. Milaeva E.R., Gerasimova O.A., Zhang J., Shpakovsky D.B., Syrbu S.A., Semeykin A.S., Koifman O.I., Kireeva E.G., Shevtsova E.F., Bachurin S.O., Zefirov N.S. J. Inorg. Biochem. 2008, 102, 1348-1358.
https://doi.org/10.1016/j.jinorgbio.2008.01.022

295. Stuzhin P.A., Hamdush M., Ziener U. Inorg. Chim. Acta 1995, 236, 131-139.
https://doi.org/10.1016/0020-1693(95)04633-K

296. Edwards W.D., Weiner B., Zerner M.C. J. Phys. Chem. 1988, 92, 6188-6197.
https://doi.org/10.1021/j100333a006

297. Korolev D.V. Abstract of the Candidate's Dissertation in Chemistry. Ivanovo: G.A. Krestov Institute of Solution Chemistry of Russian Academy of Sciences, 2012. 16 p.

298. Lomova T.N., Korolev V.V., Zakharov A.G. Mater. Sci. Eng. B 2014, 186, 54-63.
https://doi.org/10.1016/j.mseb.2014.03.006

299. Anikin M.S., Tarasov E.N., Kudrevatykh N.V., Osadchenko V.H., Zinin A.V. Acta Phys. Pol., A 2015, 127, 635-637.
https://doi.org/10.12693/APhysPolA.127.635

300. Piskorsky P., Korolev D.V., Valeev R.A., Morgunov R.B., Kunitsyna E.I. Physics and Engineering of Permanent Magnets (Kablov E.N., Ed.) Moscow: VIAM, 2018. 392 p. (in Russ.).

301. Bichan N.G., Ovchenkova E.N., Gruzdev M.S., Lomova T.N. Zh. Strukt. Khimii [Russ. J. Struct. Chem.] 2018, 59, 734-741.
https://doi.org/10.26902/JSC20180332

302. Lomova T.N., Korolev V.V., Ramazanova A.G., Balmasova O.V., Mozhzhukhina E.G. XIII Intern. Conf. «Synthesis and Applications of Porphyrins and Their Analogs» (ICPC-13), Ivanovo: Ivanovo State University of Chemistry and Technology, 2019. p. 125.

303. Lomova T.N., Andrianova L.G., Berezin B.D. Zh. Fiz. Khim. 1987, 61, 2921-2928.

304. Korolev V.V., Lomova T.N., Ramazanova A.G., Balmasova O.V., Mozhzhukhina E.G. J. Porphyrins Phthalocyanines 2019, 23, 1110-1117.
https://doi.org/10.1142/S1088424619501220

305. Gurek A.G., Basova T., Luneau D., Lebrun C., Kol'tsov E., Hassan A.K., Ahsen V. Inorg. Chem. 2006, 45, 1667-1676.
https://doi.org/10.1021/ic051754n

306. Tishin A.M., Spichcin Y.I. The Magnetocaloric Effect and Its Applications, Institute of Physics Publishing, Bristol and Philadelphia, 2003. 476 p.
https://doi.org/10.1887/0750309229

307. Korolev D.V., Korolev V.V., Lomova T.N., Mozhzhukhina E.G., Zakharov A.G. IV Regional Conference of Young Scientists Theoretical and Experimental Chemistry of Liquid-phase Systems (Krestovsky reading) Ivanovo: G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences, 2010. p. 28 (in Russ.).

308. Kudrevatykh N.V., Volegov A.S. Magnetism of Rare Earth Metals and Their Intermetallic Compounds. Yekaterinburg, 2015, 198 p. (in Russ.) [Кудреватых Н.В., Волегов А.С. Магнетизм редкоземельных металлов и их интерметаллических соединений. Екатеринбургб 2015. 198 с.].

309. Shultz D.A., Sandberg K.A. J. Phys. Org. Chem. 1999, 12, 10-18.
https://doi.org/10.1002/(SICI)1099-1395(199901)12:1<10::AID-POC85>3.0.CO;2-G

310. Xiang L.C., Liu Q., Guo C.-C., Tan Z. J. Porphyrins Phthalocyanines 2010, 14, 825-831.
https://doi.org/10.1142/S1088424610002665

311. Mironov A.F. Macroheterocycles 2011, 4, 186-208.
https://doi.org/10.6060/mhc2011.3.08

312. Yoon I., Demberelnyamba D., Li J.Z., Shim Y.K. In: Handbook of Porphyrin Science. Vol. 33. (Kadish K.M., Smith K.M., Guilard R., Eds.) Singapore: World Scientific Publishing Co Pte Ltd, 2014. p. 167.
https://doi.org/10.1142/9789814417297_0010

313. Oluwole D., Yagodin A.V., Britton J., Martynov A.G., Gorbunova Y.G., Tsivadze A.Yu., Nyokong T. Dalton Trans. 2017, 46, 16190-16198.
https://doi.org/10.1039/C7DT03867D

314. Lan Y., Klyatskaya S., Ruben M. In: Lanthanides and Actinides in Molecular Magnetism (Layfeld R.A., Murugesu M., Eds.) Wiley-VCH Verlag GmbH & Co. KGaA, 2015. p. 223.
https://doi.org/10.1002/9783527673476.ch8

315. Damjanovic' M., Morita T., Katoh K. Yamashita M., Enders M. Chem. Eur. J. 2015, 21, 14421-14432.
https://doi.org/10.1002/chem.201501944

316. Bryant D.A., Hunter C.N., Warren M.J. J. Biol. Chem. 2020, 295, 6888-6925.
https://doi.org/10.1074/jbc.REV120.006194

317. Mathew S., Yella A., Gao P., Humphry-Baker R., Curchod B.F., Ashari-Astani N., Tavernelli I., Rothlisberger U., Nazeeruddin M.K., Grätzel M. Nat. Chem. 2014, 6, 242-247.
https://doi.org/10.1038/nchem.1861

318. La Rosa M., Payne E.H., Credi A. ChemistryOpen 2020, 9, 200-213.
https://doi.org/10.1002/open.201900336

319. Lemon C.M., Karnas E., Han X., Bruns O.T., Kempa T.J., Fukumura D., Bawendi M.G., Jain R.K., Duda D.G., Nocera J. Am. Chem. Soc. 2015, 137, 9832-9842.
https://doi.org/10.1021/jacs.5b04765

320. Zenkevich E.I., Gaponenko S.V., Sagun E.I., von Borczyskowski C. Reviews in Nanoscience and Nanotechnology (Chen W., Zhao Y., Juzenas P., Eds.) USA: American Scientific Publishers, 2013, 2(3). p. 184-207.
https://doi.org/10.1166/rnn.2013.1030

321. Jeong Y.-H., Son M., Yoon H., Kim P., Lee D.-H., Kim D., Jang W.-D. Angew. Chem. Int. Ed. 2014, 53, 6925-6928.
https://doi.org/10.1002/anie.201400835

322. Shao S., Rajendiran V., Jonathan F., Lovell J.F. Coord. Chem. Rev. 2019, 379, 99-120.
https://doi.org/10.1016/j.ccr.2017.09.002

323. Zenkevich E.I., von Borczyskowski C. Formation Principles and Excited States Relaxation in Self-Assembled Complexes: Multiporphyrin Arrays and "Semiconductor CdSe/ZnS Quantum Dot-Porphyrin" Nanocomposites. In: Handbook of Porphyrin Science with Application to Chemistry, Physics, Materials Science, Engineering, Biology and Medicine. Vol. 22 - Biophysical and Physicochemical Studies of Tetrapyrroles (Kadish K., Smith K.M., Guilard R., Eds.) Singapore: World Scientific Publishing Co. Pte. Ltd., 2012. p. 67-168.
https://doi.org/10.1142/9789814397605_0006

324. Fukuzumi S., Lee Y.-M., Nam W. ChemPhotoChem 2018, 2, 121-135.
https://doi.org/10.1002/cptc.201700146

325. Hood D., Sahin T., Parkes-Loach P.S., Jiao J., Harris Michelle A., Dilbeck P., Niedzwiedzki D.M., Kirmaier C., Loach P.A., Bocian D.F., Lindsey J.S., Holten D. ChemPhotoChem 2018, 2, 300-313.
https://doi.org/10.1002/cptc.201700182

326. Lee H., Hong K.I., Jang W.D. Coord. Chem. Rev. 2018, 354, 46-73.
https://doi.org/10.1016/j.ccr.2017.06.008

327. Khadria A., Fleischhauer J., Boczarow I., Wilkinson J.D., Kohl M.M., Anderson H.L. Science 2018, 4, 153-16.
https://doi.org/10.1016/j.isci.2018.05.015

328. Huang W.B., Gu W., Huang H.X., Wang J.B., Shen W.X., Lv Y.Y., Shen J. Dyes and Pigments 2017, 143, 427-435.
https://doi.org/10.1016/j.dyepig.2017.05.001

329. Gaponenko S.V., Demir H.V. Applied Nanophotonics. Cambridge: Cambridge University Press, 2018.
https://doi.org/10.1017/9781316535868

330. Pal K. Hybrid Nanocomposites: Fundamentals, Synthesis, and Applications. USA: Jenny Stanford Publishing, 1st Edit., 2019. 412 p.
https://doi.org/10.1201/9780429000966

331. Pleus R.C., Murashov V. Physico-Chemical Properties of Nanomaterials. USA: Pan Stanford, 2018. 338 p.
https://doi.org/10.1201/9781351168601

332. Petersen N.O. Foundations for Nanoscience and Nanotechnology. London: CRC Press, 2017.
https://doi.org/10.1201/9781315381381

333. Self-Assembled Organic-Inorganic Nanostructures: Optics and Dynamics (Zenkevich E., von Borczyskowski C., Eds.) Singapore: Pan Stanford, 2016. 408 p.

334. Liu M., Voznyy O., Sabatini R., García de Arquer F.P., Munir R., Balawi A.H., Lan X., Fan F., Walters G., Kirmani A.R., Hoogland S., Laquai F., Amassian A., Sargent E.H. Nat. Mater. 2017, 16, 258-263.
https://doi.org/10.1038/nmat4800

335. Safi M., Domitrovic T., Kapur A., Zhan N., Aldeek F., Johnson J.E., Mattoussi H. Bioconjugate Chem. 2017, 28, 64−74.
https://doi.org/10.1021/acs.bioconjchem.6b00609

336. Kundu S., Patra A. Chem. Rev. 2017, 117, 712-757.
https://doi.org/10.1021/acs.chemrev.6b00036

337. Sayevich V., Guhrenz C., Dzhagan V.M., Sin M., Werheid M., Cai B., Borchardt L., Widmer J., Zahn D.R.T., Brunner E., Lesnyak V., Gaponik N., Eychmueller A. ACS Nano 2017, 11, 1559-157.
https://doi.org/10.1021/acsnano.6b06996

338. Kovalenko M.V., Manna L., Cabot, Hens Z., Talapin D.V., Kagan C.R., Klimov V.I., Rogach A.L., Reiss P., Milliron D.J., Guyot-Sionnnest P., Konstantatos G., Parak W.J., Hyeon T., Korgel B.A., Murray C.B., Heiss W. ACS Nano 2015, 9, 1012-1057.
https://doi.org/10.1021/nn506223h

339. Orlova A.O., Gromova Yu.A., Maslov V.G., Prudnikau A.V., Artemyev M.V., Fedorov A.V., Baranov A.V. J. Applied Phys. 2013, 113, 214305.
https://doi.org/10.1063/1.4809645

340. Wolfbeis O.S. Chem. Soc. Rev. 2015, 44, 4743-4768.
https://doi.org/10.1039/C4CS00392F

341. McBride J.R, Pennycook T.J., Pennycook S.J., Rosenthal S.J. ACS Nano 2013, 7, 8358-8365.
https://doi.org/10.1021/nn403478h

342. Stupak A., Blaudeck T., Zenkevich E., Krause S., von Borczyskowski C. Phys. Chem. Chem. Phys. 2018, 20, 18579-18600.
https://doi.org/10.1039/C8CP02846J

343. Plehn T., Ziemann D., May V. Phys. Chem. Chem. Phys. 2018, 20, 26870-26884.
https://doi.org/10.1039/C8CP03978J

344. Boles M.A., Ling D., Hyeon T., Talapin D.V. Nat. Mater. 2016, 15, 141-153.
https://doi.org/10.1038/nmat4526

345. Duim H., Fang H.-H., Adjokatse S., ten Brink G.H., Marques M.A.L., Kooi B.J., Blake G.R., Botti S., Loi1 M.A. Appl. Phys. Rev. 2019, 6, 031401.
https://doi.org/10.1063/1.5088342

346. Zeng B., Palui G., Zhang C., Zhan N., Wang W., Ji X., Chen B., Mattoussi H. Chem. Mater. 2018, 30, 225−238.
https://doi.org/10.1021/acs.chemmater.7b04204

347. Brown P.R., Kim D., Lunt R.R., Zhao N., Bawendi M.G., Grossman J.C., Bulovi V. ACS Nano 2014, 8, 5863-5872.
https://doi.org/10.1021/nn500897c

348. Kilin D.S., Tsemekham K., Zenkevich E.I., Prezho O.V. von Borczyskowski C. J. Photochem. Photobiol. A 2007, 190, 342-351.
https://doi.org/10.1016/j.jphotochem.2007.02.017

349. Voznyy O. J. Phys. Chem. C 2011, 115, 15927-15932.
https://doi.org/10.1021/jp205784g

350. Kilina S.V., Tamukong P.K., Kilin D.S. Acc. Chem. Res. 2016, 49, 2127−2135.
https://doi.org/10.1021/acs.accounts.6b00196

351. Zenkevich E., Shulga A., Cichos F., Petrov E.P., Blaudeck T., von Borczyskowski C. J. Phys. Chem. B 2005, 109, 8679-8692.
https://doi.org/10.1021/jp040595a

352. Blaudeck T., Zenkevich E.I., Cichos F., von Borczyskowski C. J. Phys. Chem. C 2008, 112, 20251-20257.
https://doi.org/10.1021/jp8074817

353. Blaudeck T., Zenkevich E.I., Abdel-Mottaleb M., Szwaykowska K., Kowerko D., Cichos F., von Borczyskowski C. ChemPhysChem 2012, 13, 959-972.
https://doi.org/10.1002/cphc.201100711

354. Zenkevich E.I., Blaudeck T., Kowerko D., Stupak A.P., Cichos F., von Borczyskowski C. Macroheterocycles 2012, 5, 98-114.
https://doi.org/10.6060/mhc2012.120571z

355. Zhong C., Sangwan V.K., Kang J., Luxa J., Sofer Z., Hersam M.C., Weiss E.A. J. Phys. Chem. Lett. 2019, 10, 493−499.
https://doi.org/10.1021/acs.jpclett.8b03543

356. Raevskaya A., Rozovik O., Novikova A., Selyshchev O., Stroyuk O., Dzhagan V., Goryacheva I., Gaponik N., Zahn D.R.T., Eychmüller A. RSC Adv. 2018, 8, 7550-7557.
https://doi.org/10.1039/C8RA00257F

357. Pong B.-K., Trout B.L., Lee J.-Y. Langmuir 2008, 24, 5270-5276.
https://doi.org/10.1021/la703431j

358. Schapotschnikow P., Hommersom B., Vlugt T.J.H. J. Phys. Chem. C 2009, 113, 12690-12698.
https://doi.org/10.1021/jp903291d

359. Kowerko D., Krause S., Amecke N., Abdel-Mottaleb M., Schuster J. von Borczyskowski C. Int. J. Mol. Sci. 2009, 10, 5239-5256.
https://doi.org/10.3390/ijms10125239

360. Kowerko D., Schuster J., Amecke N., Abdel-Mottaleb M., Dobrawa R., Würthner F., von Borczyskowski C. Phys. Chem. Chem. Phys. 2010, 12, 4112-4123.
https://doi.org/10.1039/b910308b

361. Chernook A.V., Shulga A.M., Zenkevich E.I., Rempel U., von Borczyskowski C. J. Phys. Chem. 1996, 100, 1918-1926.
https://doi.org/10.1021/jp951108h

362. Chernook A.V., Rempel U., von Borczyskowski C., Zenkevich E.I., Shulga A.M. Chem. Phys. Lett. 1996, 254, 229-241.
https://doi.org/10.1016/0009-2614(96)00244-8

363. Lecture Notes in Nanoscale Science and Technology. Core/Shell Quantum Dots. Synthesis, Properties and Devices Vol. 18. (Tong X., Wang Z.M., Eds.) Switzerland: Springer Nature AG. 2020.
https://doi.org/10.1007/978-3-030-46596-4

364. Zhang C., Jin Z., Zeng B., Wang W., Palui G., Mattoussi H. J. Phys. Chem. B 2020, 124, 4631−4650.
https://doi.org/10.1021/acs.jpcb.0c02177

365. Stroyuk O., Raievska O., Zahn D.R.T. Unique Luminescent Properties of Composition-/Size-Selected Aqueous Ag-In-S and Core/Shell Ag-In-S/ZnS Quantum Dots. In: Lecture Notes in Nanoscale Science and Technology. Core/Shell Quantum Dots. Synthesis, Properties and Devices. Vol. 18. (Tong X., Wang Z.M., Eds.) Switzerland: Springer Nature AG, 2020. p. 67−122.
https://doi.org/10.1007/978-3-030-46596-4_3

366. Agranovich V.M., Galanin M.D. Electronic Excitation Energy Transfer in Condensed Matter. Amsterdam, New York: North-Holland Pub. Co., 1982. 371 p.

367. Zenkevich E.I., Sagun E.I., Shulga A.M., Knyukshto V.N., Yarovoi A.A., Stupak A.P., von Borczyskowski C. Opt. Spectrosc. 2007, 103, 998−1009.
https://doi.org/10.1134/S0030400X0712020X

368. Klimov V. Nanocrystall Quantum Dots. Washington: CRS Press LLC, 2010.

369. Dabbousi B.O., Redriguez-Vejo J., Mikulec F.V., Heine J.R., Mattousi H., Ober R., Jensen K.F., Bawendi M.G. J. Phys. Chem. B 1997, 101, 9463−9475.
https://doi.org/10.1021/jp971091y

370. Zenkevich E.I., Blaudeck Th., Heidernätsch M., Cichos F., von Borczyskowski C. Theor. Exper. Chem. 2009, 45, 23-34.
https://doi.org/10.1007/s11237-009-9058-9

371. Zenkevich E.I., Stupak A.P., Kowerko D., von Borczyskowski C. Chem. Phys. 2012, 406, 21−29.
https://doi.org/10.1016/j.chemphys.2012.02.008

372. Zenkevich E., Stupak A., Göhler C., Krasselt C., von Borczyskowski C. ACS Nano 2015, 9, 2886−2903.
https://doi.org/10.1021/nn506941c

373. Inerbaev T.M., Masunov A.E., Khondaker S.I., Dobrinescu A., Plamadă A.-V., Kawazoe Y. J. Chem. Phys. 2009, 131, 044106.
https://doi.org/10.1063/1.3135193

374. Kilina S., Kilin D., Tretiak S. Chem. Rev. 2015, 115, 5929-5978.
https://doi.org/10.1021/acs.chemrev.5b00012

375. Dayal S., Burda C. J. Am. Chem. Soc. 2007, 129, 7977−7981.
https://doi.org/10.1021/ja071457c

376. Liptay T.J., Ram R.J. Appl. Phys. Lett. 2006, 89, 223132.
https://doi.org/10.1063/1.2400107

377. De Mello Donegá. Nanoparticles. Berlin, Heidelberg: Springer-Verlag, 2014.
https://doi.org/10.1007/978-3-662-44823-6

378. Fischer T., Heinrich K., Spudat C., Martin J., Otto T., Gessner T., Kroll L. Microelectron. Eng. 2015, 146, 57−61.
https://doi.org/10.1016/j.mee.2015.03.064

379. Möbius M., Ma X.-Y., Martin J., Doty M.F., Otto T., Gessner T. Proc. SPIE 2015, 9370, 93701X.
https://doi.org/10.1117/12.2185047

380. Möbius M., Martin J., Hartwig M., Baumann R.R., Otto T., Gessner T. AIP Adv. 2016, 6, 085309.
https://doi.org/10.1063/1.4961145

381. Korten T., Nitzsche B., Gell C., Ruhnow F., Leduc C., Diez S. Fluorescence Imaging of Single Kinesin Motors on Immobilized Microtubules. In: Methods in Molecular Biology (Single Molecule Analysis) Vol. 783. (Peterman E., Wuite G., Eds.) Springer Protocols: Humana Press, 2011. p. 121-137.
https://doi.org/10.1007/978-1-61779-282-3_7

382. Korten S., Albet-Torres N., Paderi F., ten Siethoff L., Diez S., Korten T., te Kronnie G., Månsson A. Lab Chip 2013, 13, 866-876.
https://doi.org/10.1039/c2lc41099k

383. Selyshchev O., Dzhagan V., Zenkevich E., Stroyuk A., Raevskaya A., Sheinin V., Kulikova O., Koifman O., Zahn D.R.T. Electronic Interaction Between Ag-In-S, Ag-In-S/ZnS Quantum Dots and Quaternary Amine Aromatic Molecules - A Photoluminescence Quenching Study. In: Book of Abstracts of the 14th International Symposium on Functional π-Electron Systems (June 2-7) 2019, Berlin. p. #106.

384. Sheinin V., Kulikova O., Zenkevich E., Selyshchev O., Dzhagan V., Stroyuk A., Raevskaya A., Koifman O., Zahn D.R.T. Tetra(N-methyl-4-pyridyl)porphyrin Sonde Report on the Surface of AIS/ZnS/GSH Quantum Dots in Water. In: Book of Abstr. of the 1st International Conference on Noncovalent Interactions (2-6 September) 2019, Lisbon. p. P82.

385. Zenkevich E., Sheinin V., Kulikova O., Selyshchev O., Dzhagan V., Stroyuk O., Raievska O., Koifman O., von Borczyskowski C., Zahn D.R.T. Self-Assembled Nanocomposites Based on Semiconductor Quantum Dots and Porphyrin Molecules: Interface Chemistry, Optical Properties and Energy Relaxation Processes. In: Book of Abstracts of Webinar on Materials Science and Nanotechnology. Coalesce Research Group, 33 Market Point Dr., Greenwille SC 29607, USA (July 29-30) 2020. p. 11.

386. Carella A., Borbone F., Centore R. Front. Chem. 2018, 6, 481.
https://doi.org/10.3389/fchem.2018.00481

387. Arooj Q., Wilson G.J., Wang F. Materials 2019, 12, 4024.
https://doi.org/10.3390/ma12244024

388. Iftikhar H., Sonai G.G., Hashmi S.G., Nogueira A.F., Lund P.D. Materials 2019, 12, 1998.
https://doi.org/10.3390/ma12121998

389. Widhiyanuriyawan D., Trihutomo P., Soeparman S., Yuliati L. Scientific World Journal 2020, 2020, 7910702.
https://doi.org/10.1155/2020/7910702

390. Koyyada G., Chitumalla R.K., Thogiti S., Kim J.H., Jang J., Chandrasekharam M., Jung J.H. Molecules 2019, 24, 3554.
https://doi.org/10.3390/molecules24193554

391. Luceño-Sánchez J.A., Díez-Pascual A.M., Capilla R.P. Int. J. Mol. Sci. 2019, 20, 976.
https://doi.org/10.3390/ijms20040976

392. Ezhov A.V., Vyalba F.Yu., Zhdanova K.A., Mironov A.F., Zhizhin K.Yu., Bragina N.A. Fine Chemical Technologies 2018, 13(2), 21-30. (in Russ.).
https://doi.org/10.32362/2410-6593-2018-13-2-21-30

393. Longo C., De Paoli M.-A. J. Braz. Chem. Soc. 2003, 14(6), 889-901.
https://doi.org/10.1590/S0103-50532003000600005

394. Ezhov A.V., Zhdanova K.A., Bragina N.A., Mironov A.F. Macroheterocycles 2016, 9(4), 337-352.
https://doi.org/10.6060/mhc160752e

395. Vittal R., Ho K.-C. Renewable and Sustainable Energy Reviews 2017, 70, 920-935.
https://doi.org/10.1016/j.rser.2016.11.273

396. Eguchi K., Koga H., Sekizawa K., Sasaki K. J. Ceramic Soc. Japan 2000, 108(12), 1067-1071.
https://doi.org/10.2109/jcersj.108.1264_1067

397. Septiawan T.Y., Sumardiasih S., Obina W.M., Supriyanto A., Khairuddin, Cari C. AIP Conference Proceedings 2017, 1868, 060010.
https://doi.org/10.1063/1.4995174

398. Banik A., Ansari M.S., Qureshi M. ACS Omega 2018, 3, 14482-14493.
https://doi.org/10.1021/acsomega.8b02520

399. Saeidi M., Abrari M., Ahmadi M. Appl. Phys. A 2019, 125, 409.
https://doi.org/10.1007/s00339-019-2697-3

400. Valerio T.L., Maia G.A.R., Gonçalves L.F., Viomar A., Banczek E. do P., Rodrigues P.R.P. Mater. Res. 2019, 22(suppl. 1), e20180864.
https://doi.org/10.1590/1980-5373-mr-2018-0864

401. Chen L.H., Xue B.F., Luo Y.H. Chin. Phys. Lett. 2007, 24(2), 555-558.

402. Chen D., Zhang Q., Wang G. Electrochem. Commun. 2007, 9, 2755-2759.
https://doi.org/10.1016/j.elecom.2007.09.013

403. Jung Y.S., Yoo B., Lim M.K., Kim K.J. Electrochim. Acta 2009, 54, 6286-6291.
https://doi.org/10.1016/j.electacta.2009.06.006

404. Gu P., Yang D., Zhu X., Sun H., Wangyang P., Li J., Tian H. AIP Adv. 2017, 7, 105219.
https://doi.org/10.1063/1.5000564

405. Lu J.F., Bai J., Xu X.B., Li Z.H., Cao K., Cui J., Wang M.K. Chin. Sci. Bull. 2012, 57(32), 4131-4142.
https://doi.org/10.1007/s11434-012-5409-3

406. Wang M., Grätzel C., Zakeeruddin S.M., Grätzel M. Energy Environ. Sci. 2012, 5, 9394-9405.
https://doi.org/10.1039/c2ee23081j

407. Stergiopoulos T., Rozi E., Karagianni C.-S., Falaras P. Nanoscale Res. Lett. 2011, 6, 307.
https://doi.org/10.1186/1556-276X-6-307

408. Cao Y., Zhang J., Bai Y., Li R., Zakeeruddin S.M., Grätzel M., Wang P. J. Phys. Chem., C 2008, 112, 13775-13781.
https://doi.org/10.1021/jp805027v

409. Önen T., Karakuş M.Ö., Coşkun R., Çetin H. J. Photochem. Photobiol., A: Chemistry 2019, 385, 112082.
https://doi.org/10.1016/j.jphotochem.2019.112082

410. Shen S.-Y., Dong R.-X., Shih P.-T., Ramamurthy V., Lin J.-J., Ho K.-C. ACS Appl. Mater. Interfaces 2014, 6(21), 18489-18496.
https://doi.org/10.1021/am505394v

411. Pujiarti H., Arsyad W.S., Shobih, Muliani L., Hidayat R. IOP Conf. Series: J. Physics: Conf. Series 2018, 1011, 012020.
https://doi.org/10.1088/1742-6596/1011/1/012020

412. Duan Y., Tang Q., Chen Y., Zhao Z., Lv Y., Hou M., Yang P., He B., Yu L. J. Mater. Chem., A 2015, 3, 5368-5374.
https://doi.org/10.1039/C4TA06393G

413. Nam S.-H., Lee K.H., Yu J.-H., Boo J.-H. Appl. Sci. Converg. Technol. 2019, 28(6), 194-206.
https://doi.org/10.5757/ASCT.2019.28.6.194

414. Shalini S., Balasundaraprabhu R., Satish Kumar T., Prabavathy N., Senthilarasu S., Prasanna S. Int. J. Energy Res. 2016, 40, 1303-1320.
https://doi.org/10.1002/er.3538

415. Sharma K., Sharma V., Sharma S.S. Nanoscale Res. Lett. 2018, 13, 381.
https://doi.org/10.1186/s11671-018-2760-6

416. Qin Y., Peng Q. Int. J. Photoenergy 2012, 2012, 291579.
https://doi.org/10.1155/2012/291579

417. Abate A., Planells M., Hollman D.J., Stranks S.D., Petrozza A., Kandada A.R.S., Vaynzof Y., Pathak S.K., Robertson N., Snaith H.J. Adv. Energy Mater. 2014, 4, 1400166.
https://doi.org/10.1002/aenm.201400166

418. Hu Y., Ivaturi A., Planells M., Boldrini C.L., Biroli A.O., Robertson N. J. Mater. Chem., A 2016, 4, 2509.
https://doi.org/10.1039/C5TA09133K

419. Hwang S., Lee J.H., Park C., Lee H., Kim C., Park C., Lee M.H., Lee W., Park J., Kim K., Park N.G., Kim C. Chem. Commun. 2007, 46, 4887.
https://doi.org/10.1039/b709859f

420. Mane S.B., Cheng C.F., Sutanto A.A., Datta A., Dutta A., Hung C.H. Tetrahedron 2015, 71, 7977.
https://doi.org/10.1016/j.tet.2015.08.068

421. Al-horaibi S.A., Gaikwad S.T., Rajbhoj A.S. Adv. Mat. Lett. 2018, 9(5), 353-362.
https://doi.org/10.5185/amlett.2018.1740

422. Chen G., Sasabe H., Igarashi T., Hong Z., Kido J. J. Mater. Chem., A 2015, 3, 14517.
https://doi.org/10.1039/C5TA01879J

423. Khopkar S., Shankarling G. Dyes and Pigments 2019, 170, 107645.
https://doi.org/10.1016/j.dyepig.2019.107645

424. Qin C., Wong W.-Y., Han L. Chem. Asian. J. 2013, 8, 1706-1719.
https://doi.org/10.1002/asia.201300185

425. Jamalullail N., Mohamad I.S., Norizan M.N., Baharum N.A. IEEE 15th Student Conference on Research and Development (SCOReD) 2017, 344-349.

426. Pamain A., Pogrebnaya T., King'ondu C.K. Res. J. Eng. Appl. Sci. 2014, 3(5), 332-336.

427. Liu Q., Gao N., Liu D., Liu J., Li Y. Appl. Sci. 2018, 8, 1697.
https://doi.org/10.3390/app8091697

428. Selopal G.S., Wu H.-P., Lu J., Chang Y.-C., Wang M., Vomiero A., Concina I., Diau E.W.-G. Scientific Reports 2016, 6, 18756.
https://doi.org/10.1038/srep18756

429. Tsao H.N., T. Moehl C.Yi, Yum J.H., Zakeeruddin S.M., Nazeeruddin M.K., Grätzel M., ChemSusChem 2011, 4, 591-594 DOI: 10.1002/cssc.201100120

430. Angaridis P., Lazarides T., Coutsolelos A.C. Polyhedron 2014, 82, 19-32.
https://doi.org/10.1016/j.poly.2014.04.039

431. Ladomenou K., Kitsopoulos T.N., Sharma G.D., Coutsolelos A.G. RSC Adv. 2014, 4, 21379-21404.
https://doi.org/10.1039/C4RA00985A

432. Obraztsov I., Kutner W., D'Souza F. Sol. RRL 2017, 1, 1600002.
https://doi.org/10.1002/solr.201600002

433. Zhang L., Cole J.M. ACS Appl. Mater. Interfaces 2015, 7(6), 3427-3455.
https://doi.org/10.1021/am507334m

434. Daphnomili D., Landrou G., Singh S.P., Thomas A., Yesudas K., Bhanuprakash K., Sharma G.D., Coutsolelos A.G. RSC Adv. 2012, 2, 12899-12908.
https://doi.org/10.1039/c2ra22129b

435. Lu J., Xu X., Li Z., Cao K., Cui J., Zhang Y., Shen Y., Li Y., Zhu J., Dai S., Chen W., Cheng Y., Wang M. Chem. Asian. J. 2013, 8, 956-962.
https://doi.org/10.1002/asia.201201136

436. Mai C.-L., Moeh T., Hsieh C.-H., Decoppet J.-D., Zakeeruddin S.M., Grätzel M., Yeh C.-Y. ACS Appl. Mater. Interfaces 2015, 7(27), 14975-14982.
https://doi.org/10.1021/acsami.5b03783

437. Brennan B.J., Portolés M.J.L., Liddell P.A., Moore T.A., Moore A.L., Gust D. Phys. Chem. Chem. Phys. 2013, 15, 16605-16614.
https://doi.org/10.1039/c3cp52156g

438. Odobel F., Blart E., Lagrée M., Villieras M., Boujtita H., El Murr N., Caramoric S., Bignozzi C.A. J. Mater. Chem. 2003, 13, 502-510.
https://doi.org/10.1039/b210674d

439. López-Duarte I., Wang M., Humphry-Baker R., Ince M., Martínez-Díaz M.V., Nazeeruddin M.K., Torres T., Grätzel M. Angew. Chem. Int. Ed. 2012, 51, 1895-1898.
https://doi.org/10.1002/anie.201105950

440. He H., Gurunga A., Si L. Chem. Commun. 2012, 48, 5910-5912.
https://doi.org/10.1039/c2cc31440a

441. Ma T., Inoue K., Noma H., Yao K., Abe E. J. Photochem. Photobiol., A: Chemistry 2002, 152, 207-212.
https://doi.org/10.1016/S1010-6030(02)00025-4

442. Gou F., Jiang X., Li B., Jing H.-W., Zhu Z. ACS Appl. Mater. Interfaces 2013, 5(23), 12631-12637.
https://doi.org/10.1021/am403987b

443. Gou F., Jiang X., Fang R., Jing H., Zhu Z. ACS Appl. Mater. Interfaces 2014, 6, 6697-6703.
https://doi.org/10.1021/am500391w

444. Zhang N., Zhang B., Yan J., Xue X., Peng X., Li Y., Yang Y., Ju C., Fan C., Feng Y. Renewable Energy 2015, 77, 579-585.
https://doi.org/10.1016/j.renene.2014.12.066

445. Keawin T., Tarsang R., Sirithip K., Prachumrak N., Sudyoadsuk T., Namuangruk S., Roncali J., Kungwan N., Promarak V., Jungsuttiwong S. Dyes and Pigments 2017, 136, 697-706.
https://doi.org/10.1016/j.dyepig.2016.09.035

446. Ishida M., Park S.W., Hwang D., Koo Y.B., Sessler J.L., Kim D.Y., Kim D. J. Phys. Chem., C 2011, 115, 19343-19354.
https://doi.org/10.1021/jp202307b

447. Matsuzaki H., Murakami T.N., Masaki N., Furube A., Kimura M., Mori S. J. Phys. Chem., C 2014, 118, 17205-17212.
https://doi.org/10.1021/jp500798c

448. Si L., He H. J. Phys. Chem., A 2014, 118(19), 3410-3418.
https://doi.org/10.1021/jp412609k

449. Imahori H., Hayashi S., Hayashi H., Oguro A., Eu S., Umeyama T., Matano Y. J. Phys. Chem., C 2009, 113, 18406-18413.
https://doi.org/10.1021/jp907288h

450. Kroeze J.E., Hirata N., Koops S., Nazeeruddin Md.K., Schmidt-Mende L., Grätzel M., Durrant J.R. J. Am. Chem. Soc. 2006, 128(50), 16376-16383.
https://doi.org/10.1021/ja065653f

451. Zhang L., Cole J.M. J. Mater. Chem., A 2017, 5, 19541-19559.
https://doi.org/10.1039/C7TA05632J

452. Xue X., Zhang W., Zhang N., Ju C., Peng X., Yang Y., Liang Y., Feng Y., Zhang B. RSC Adv. 2014, 4, 8894-8900.
https://doi.org/10.1039/c3ra46212a

453. Chen J., Ko S., Liu L., Sheng Y., Han H., Li X. New J. Chem. 2015, 39, 3736-3746.
https://doi.org/10.1039/C4NJ02263G

454. Lu F., Zhang J., Zhou Y., Zhao Y., Zhang B., Feng Y. Dyes and Pigments 2016, 125, 116-123.
https://doi.org/10.1016/j.dyepig.2015.10.010

455. Magnano G., Marinotto D., Cipolla M.P., Trifiletti V., Listorti A., Mussini P.R., Di Carlo G., Tessore F., Manca M., Orbelli Biroli A., Pizzotti M. Phys. Chem. Chem. Phys. 2016, 18, 9577-9585.
https://doi.org/10.1039/C6CP00129G

456. Higashino T., Kawamoto K., Sugiura K., Fujimori Y., Tsuji Y., Kurotobi K., Ito S., Imahori H. ACS Appl. Mater. Interfaces 2016, 8(24), 15379-15390.
https://doi.org/10.1021/acsami.6b03806

457. Ananthakumar S., Balaji D., Kumar J.R., Babu S.M. SN Appl. Sci. 2019, 1, 186.
https://doi.org/10.1007/s42452-018-0054-3

458. Bessho T., Zakeeruddin S.M., Yeh C.-Y., Diau E.W.-G., Grätzel M. Angew. Chem. Int. Ed. 2010, 49, 6646-6649.
https://doi.org/10.1002/anie.201002118

459. Michaels H., Rinderle M., Freitag R., Benesperi I., Edvinsson T., Socher R., Gagliardi A., Freitag M. Chem. Sci. 2020, 11, 2895-2906.
https://doi.org/10.1039/C9SC06145B

460. Truta L.A.A.N.A., Moreira F.T.C., Sales M.G.F. Biosens. Bioelectron. 2018, 107, 94-102.
https://doi.org/10.1016/j.bios.2018.02.011

461. Guo W., Xue X., Wang S., Lin C., Wang Z.L. Nano Lett. 2012, 12, 2520-2523.
https://doi.org/10.1021/nl3007159

462. Pu X., Song W., Liu M., Sun C., Du C., Jiang C., Huang X., Zou D., Hu W., Wang Z.L. Adv. Energy Mater. 2016, 6, 1601048.
https://doi.org/10.1002/aenm.201601048

463. Yun S., Qin Y., Uhl A.R., Vlachopoulos N., Yin M., Li D., Han X., Hagfeldt A. Energy Environ. Sci. 2018, 11, 476-526.
https://doi.org/10.1039/C7EE03165C

464. Honda K, Fujishima A. Nature 1972, 238, 37-38.
https://doi.org/10.1038/238037a0

465. Watanabe M. Sci. Technol. Adv. Mater. 2017, 18(1), 705-723.
https://doi.org/10.1080/14686996.2017.1375376

466. Youngblood W.J., Lee S.-H.A., Maeda K., Mallouk T.E. Acc. Chem. Res. 2009, 42(12), 1966-1973.
https://doi.org/10.1021/ar9002398

467. Gan J., Lu X., Tong Y. Nanoscale 2014, 6, 7142-7164.
https://doi.org/10.1039/c4nr01181c

468. Abe R. J. Photochem. Photobiol., C: Photochem. Rev. 2010, 11, 179-209.
https://doi.org/10.1016/j.jphotochemrev.2011.02.003

469. Yun S., Vlachopoulos N., Qurashi A., Ahmad S., Hagfeldt A. Chem. Soc. Rev. 2019, 48, 3705-3722.
https://doi.org/10.1039/C8CS00987B

470. Swierk J.R., Mallouk T.E. Chem. Soc. Rev. 2013, 42, 2357-2387.
https://doi.org/10.1039/C2CS35246J

471. Swierk J.R., Méndez-Hernádez D.D., McCool N.S., Liddell P., Terazono Y., Pahk I., Tomlin J.J., Oster N.V., Moore T.A., Moore A.L., Gust D., Mallouk T.E. Proc. Nat. Acad. Sci. 2015, 112(6), 1681-1686.
https://doi.org/10.1073/pnas.1414901112

472. Sherman B.D., Bergkamp J.J., Brown C.L., Moore A.L., Gust D., Moore T.A. Energy Environ Sci. 2016, 9, 1812-1817.
https://doi.org/10.1039/C6EE00258G

473. Kang S.H., Jeong M.J., Eom Y.K., Choi I.T., Kwon S.M., Yoo Y., Kim J., Kwon J., Park J.H., Kim H.K. Adv. Energy Mater. 2017, 7, 1602117.
https://doi.org/10.1002/aenm.201602117

474. Melville O.A., Lessard B.H., Bender T.P. ACS Appl. Mater. Interfaces 2015, 7, 13105−13118.
https://doi.org/10.1021/acsami.5b01718

475. de la Torre G., Bottari G., Torres T. Adv. Energy Mater. 2017, 7(10), 1601700.
https://doi.org/10.1002/aenm.201601700

476. Brinkmann H., Kelting C., Makarov S., Tsaryova O., Schnurpfeil G., Wöhrle D., Schlettwein D. Phys. Status Solidi (A) Appl. Mater. Sci. 2008, 205(3), 409−420.
https://doi.org/10.1002/pssa.200723391

477. Stuzhin P.A. Fluorinated Phthalocyanines and Their Analogues In: Fluorine in Heterocyclic Chemistry. Vol. 1. 5-Membered Heterocycles and Macrocycles. (Nenajdenko V.G., Ed.). Heidelberg: Springer, 2014. p. 621−681.
https://doi.org/10.1007/978-3-319-04346-3_15

478. Stuzhin P.A., Ercolani C. Porphyrazines with Annulated Heterocycles. In: Porphyrin Handbook. Vol. 15. (Kadish K.M., Smith K.M., Guilard R., Ed.) Amsterdam: Elsevier Science, 2003. p. 263−364.
https://doi.org/10.1016/B978-0-08-092389-5.50011-0

479. Donzello M.P., Ercolani C., Novakova V., Zimcik P., Stuzhin P.A. Coord. Chem. Rev. 2016, 309, 107−179.
https://doi.org/10.1016/j.ccr.2015.09.006

480. Novakova V., Donzello M.P., Ercolani C., Zimcik P., Stuzhin P.A. Coord. Chem. Rev. 2018, 361, 1−73.
https://doi.org/10.1016/j.ccr.2018.01.015

481. Lonchakov A.V., Rakitin O.A., Gritsan N.P., Zibarev A.V. Molecules 2013, 18(8), 9850−9900.
https://doi.org/10.3390/molecules18089850

482. Rakitin O.A. Tetrahedron Lett. 2020, 61(34), 152230.
https://doi.org/10.1016/j.tetlet.2020.152230

483. Konstantinova L.S., Knyazeva E.A., Rakitin O.A. Rev. Org. Preparations and Procedures Int. 2014, 46(6), 475−544.
https://doi.org/10.1080/00304948.2014.963454

484. Stuzhin P.A., Bauer E.M., Ercolani C. Inorg. Chem. 1998, 37(7), 1533−1539.
https://doi.org/10.1021/ic9609259

485. Bauer E.M., Ercolani C., Galli P., Popkova I.A., Stuzhin P.A. J. Porphyrins Phthalocyanines 1999, 3(5), 371−379.
https://doi.org/10.1002/(SICI)1099-1409(199906)3:5<371::AID-JPP140>3.0.CO;2-F

486. Donzello M.P., Ercolani C., Stuzhin P.A. Coord. Chem. Rev. 2006, 250(11-12), 1530-1561.
https://doi.org/10.1016/j.ccr.2006.02.009

487. Cozzolino A., Yang Q., Vargas-Baca I. Cryst. Growth Des. 2010, 10, 4959-4964.
https://doi.org/10.1021/cg101060s

488. Stuzhin P.A., Mikhailov M.S., Yurina E.S., Bazanov M.I., Koifman O.I., Pakhomov G.L., Travkin V.V., Sinelshchikova A.A. Chem. Comm. 2012, 48(81), 10135-10137.
https://doi.org/10.1039/c2cc35580a

489. Otlyotov A.A., Ryzhov I.V., Kuzmin I.A., Zhabanov Y.A., Mikhailov M.S., Stuzhin P.A. Int. J. Molec. Sci. 2020, 21(8), 2923.
https://doi.org/10.3390/ijms21082923

490. Stuzhin P.A., Ivanova S.S., Hamdoush M., Kirakosyan G.A., Kiselev A., Popov A., Sliznev V., Ercolani C. Dalton Trans. 2019, 48(37), 14049-14061.
https://doi.org/10.1039/C9DT02345C

491. Bauer E.M., Cardarilli D., Ercolani C., Stuzhin P.A., Russo U. Inorg. Chem. 1999, 38(26), 6114-6120.
https://doi.org/10.1021/ic990855g

492. Pia Donzello M., Viola E., Giustini M., Ercolani C., Monacelli F. Dalton Trans. 2012, 41(20), 6112-6121.
https://doi.org/10.1039/c2dt12381a

493. Angeloni S., Bauer E.M., Ercolani C., Popkova I.A., Stuzhin P.A. J. Porphyrins Phthalocyanines 2001, 5(12), 881-888.
https://doi.org/10.1002/jpp.558

494. Tarakanova E.N., Hamdoush M., Eroshin A.V., Ryzhov I.V., Zhabanov Y.A., Stuzhin P.A. Polyhedron 2021, 193, 114877.
https://doi.org/10.1016/j.poly.2020.114877

495. Donzello M.P., Agostinetto R., Ivanova S.S., Fujimori M., Suzuki Y., Yoshikawa H., Shen J., Awaga K., Ercolani C., Kadish K.M., Stuzhin P.A. Inorg. Chem. 2005, 44(23), 8539-8551.
https://doi.org/10.1021/ic050866b

496. Miyoshi Y., Takahashi K., Fujimoto T., Yoshikawa H., Matsushita M.M., Ouchi Y., Kepenekian M., Robert V., Donzello M.P., Ercolani C., Awaga K. Inorg. Chem. 2012, 51(1), 456-462.
https://doi.org/10.1021/ic201880g

497. Onay H., Yerli Y., Öztürk R. Transition Met. Chem. 2009, 34(2), 163-166.
https://doi.org/10.1007/s11243-008-9172-x

498. Hamdoush M., Ivanova S.S., Pakhomov G.L., Stuzhin P.A. Macroheterocycles 2016, 9(3), 230-233.
https://doi.org/10.6060/mhc160424s

499. Hamdoush M., Nikitin K., Skvortsov I., Somov N., Zhabanov Yu., Stuzhin P.A. Dyes and Pigments 2019, 170, 107584.
https://doi.org/10.1016/j.dyepig.2019.107584

500. Kudrik E.V., Bauer E.M., Ercolani C., Chiesi-Villa A., Rizzoli C., Gaberkorn A., Stuzhin P.A. Mendeleev Commun. 2001, 11(2), 45-47.
https://doi.org/10.1070/MC2001v011n02ABEH001372

501. Donzello M.P., Ercolani C., Gaberkorn A.A., Kudrik E.V., Meneghetti M., Marcolongo G., Rizzoli C., Stuzhin P.A. Chem. Eur. J. 2003, 9(17), 4009-4024.
https://doi.org/10.1002/chem.200304929

502. Gaberkorn A.A., Donzello M.-P., Stuzhin P.A. Russ. J. Org. Chem. 2006, 42(6), 929-935.
https://doi.org/10.1134/S1070428006060200

503. Stuzhin P.A., Pimkov I.V., Ul-Haq A., Ivanova S.S., Popkova I.A., Volkovich D.I., Kuzmitskii V.A., Donzello M.-P. Russ. J. Org. Chem. 2007, 43(12), 1854-1863.
https://doi.org/10.1134/S1070428007120202

504. Svec J., Zimcik P., Novakova L., Rakitin O.A., Amelichev S., Stuzhin P.A., Novakova V. Eur. J. Org. Chem. 2015, 3, 596-604.
https://doi.org/10.1002/ejoc.201403329

505. Stuzhin P.A. Synthesis, Structure and Physico-chemical properties of Azaporphyrins and Porphyrazines. Diss. doc. chem sci. Ivanovo: ISUCT, 2004.

506. Volkovich D.I., Kuzmitsky V.A., Stuzhin P.A. J. Appl. Spectrosc. 2008, 75(5), 621-636.
https://doi.org/10.1007/s10812-008-9113-7

507. Cai X., Zhang Y., Zhang X., Jiang J. J. Molec. Struc.: THEOCHEM 2007, 812(1-3), 63-70.
https://doi.org/10.1016/j.theochem.2007.02.010

508. Donzello M.-P., Ercolani C., Kadish K.M., Ricciardi G., Rosa A., Stuzhin P.A. Inorg. Chem. 2007, 46(10), 4145-4157.
https://doi.org/10.1021/ic070038d

509. Tverdova N.V., Giricheva N.I., Savelyev D.S., Mikhailov M.S., Vogt N., Koifman O.I., Stuzhin P.A., Girichev G.V. Macroheterocycles 2017, 10(1), 27-30.
https://doi.org/10.6060/mhc170399g

510. Zhabanov Y.A., Sliznev V.V., Ryzhov I.V., Stuzhin P.A. J. Porphyrins Phthalocyanines 2020, 24(9), 1146-1154.
https://doi.org/10.1142/S1088424620500285

511. Zhabanov Yu.A., Tverdova N.V., Giricheva N.I., Girichev G.V., Stuzhin P.A. J. Porphyrins Phthalocyanines 2017, 21(4-6), 439-452.
https://doi.org/10.1142/S1088424617500444

512. Fujimori M., Suzuki Y., Yoshikawa H., Awaga K. Angew. Chem. Int. Ed. 2003, 42(47), 5863-5865.
https://doi.org/10.1002/anie.200352571

513. Suzuki Y., Fujimori M., Yoshikawa H., Awaga K. Chem. Eur. J. 2004, 10(20), 5158-5164.
https://doi.org/10.1002/chem.200400394

514. Donzello M.P., Fujimori M., Miyoshi Y., Yoshikawa H., Viola E., Awaga K., Ercolani C. J. Porphyrins Phthalocyanines 2010, 14(4), 343-348.
https://doi.org/10.1142/S1088424610002082

515. Miyoshi Y., Kubo M., Fujinawa T., Suzuki Y., Yoshikawa H., Awaga K. Angew. Chem. Int. Ed. 2007, 46(29), 5532-5536.
https://doi.org/10.1002/anie.200700702

516. Eguchi K., Heutz S., Awaga K. J. Porphyrins Phthalocyanines 2017, 21(4-6), 322-326.
https://doi.org/10.1142/S1088424617500171

517. Eguchi K., Nanjo C., Awaga K., Tseng H.-H., Robaschik P., Heutz S. Phys. Chem. Chem. Phys. 2016, 18(26), 17360-17365.
https://doi.org/10.1039/C6CP01932C

518. Stuzhin P.A., Mikhailov M.S., Travkin V.V., Gudkov E.Y., Pakhomov G.L. Macroheterocycles 2012, 5(2), 162-165.
https://doi.org/10.6060/mhc2012.120573p

519. Stuzhin P.A., Mikhailov M.S., Travkin V.V., Pakhomov G.L. Zinc(II) Tetra(1,2,5-thiadiazolo)porphyrazine Complex in Thin Film Photovoltaic Structures. In: Recent Developments in Coordination, Bioinorganic, and Applied Inorganic Chemistry. Vol. 11. (Melnik M., Segl'a P., Tatarko M., Eds.) Bratislava: Press of Slovak University of Technology, 2013. p. 318-323. ISBN 978-80-227-3918-4.
https://doi.org/10.13140/2.1.2341.3761

520. Hou J., Wang Y., Eguchi K., Nanjo C., Takaoka T., Sainoo Y., Awaga K., Komeda T. Appl. Surface Sci. 2018, 440, 16-19.
https://doi.org/10.1016/j.apsusc.2018.01.001

521. Wang Y., Hou J., Eguchi K., Nanjo C., Takaoka T., Sainoo Y., Awaga K., Komeda T. ACS Omega 2020, 5(12), 6676-6683.
https://doi.org/10.1021/acsomega.9b04453

522. Miyoshi Y., Fujimoto T., Yoshikawa H., Matsushita M.M., Awaga K., Yamada T., Ito H. Org. Electron. 2011, 12(2), 239-243.
https://doi.org/10.1016/j.orgel.2010.11.005

523. Fujimoto T., Miyoshi Y., Matsushita M.M., Awaga K. Chem. Commun. 2011, 47(20), 5837-5839.
https://doi.org/10.1039/c0cc05198e

524. Nanjo C., Fujimoto T., Matsushita M.M., Awaga K. J. Phys. Chem., C 2014, 118(26), 14142-14149.
https://doi.org/10.1021/jp502056s

525. Koptyaev A.I., Khamdoush M., Fedoseev A.N., Travkin V.V., Pakhomov G.L. Macroheterocycles 2018, 11(4), 412-417.
https://doi.org/10.6060/mhc181114p

526. Pakhomov G.L., Travkin V.V., Hamdoush M., Zhabanov Yu.A., Stuzhin P.A. Macroheterocycles 2017, 10(4-5), 548-551.
https://doi.org/10.6060/mhc171038s

527. Park J.M., Lee J.H., Jang W.-D. Coord. Chem. Rev. 2020, 407, 213157-213185.
https://doi.org/10.1016/j.ccr.2019.213157

528. Konovalova N.V., Evstigneeva R.P., Luzgina V.N. Russ. Chem. Rev. 2001, 70, 939-970.
https://doi.org/10.1070/RC2001v070n11ABEH000682

529. Borovkov V.V., Mamardashvili N.Zh., Inoue Y. Russ. Chem. Rev. 2006, 75, 737-748.
https://doi.org/10.1070/RC2006v075n08ABEH003630

530. Kruk N.N. J. Appl. Spectrosc. 2008, 75, 461-482.
https://doi.org/10.1007/s10812-008-9088-4

531. Flamigni L., Gryko D.T. Chem. Soc. Rev. 2009, 38, 1635-1646.
https://doi.org/10.1039/b805230c

532. De Souza F., Chitta R., Ohkubo K. et al. J. Am. Chem. Soc. 2008, 130, 14263-14272.
https://doi.org/10.1021/ja804665y

533. Adeyemi O.O., Malinovskii V.L., Biner S.M. et al. Chem. Commun. 2012, 48, 9589-9591.
https://doi.org/10.1039/c2cc34183b

534. Andrianova L.G., Lomova T.N., Berezin B.D. Zhurn. Neorgan. Khimii 1984, 29, 1697-1701. (in Russ.).

535. Miyazaki Y., Satake A., Kobuke Y. J. Mol. Cat. A: Chem. 2008, 283, 129-139.
https://doi.org/10.1016/j.molcata.2007.12.016

536. Ni Y., Marchal G., Yu G. et al. Acad. Radiol. 1995, 2, 687-699.
https://doi.org/10.1016/S1076-6332(05)80437-4

537. He H., Zhu X., Hou A. Dalton Trans. 2004, 23, 4064-4073.
https://doi.org/10.1039/B410600H

538. He H., Wong W.-K., Li K.-F., Cheah K.-W. Synth. Met. 2004, 143, 81-87.
https://doi.org/10.1016/j.synthmet.2003.10.011

539. He H., Sykes A.G., May P.S., He G. Dalton Trans. 2009, 36, 7454-7461.
https://doi.org/10.1039/B909243A

540. Foley T., Harrison B., Knefely A. et al. Inorg. Chem. 2003, 42, 5023-5032.
https://doi.org/10.1021/ic034217g

541. Xin Z., Wei L., Ming J., Fa L. Synth. React. Inorg. Met. Org. Nano-Met. Chem. 2000, 30, 1747-1758.
https://doi.org/10.1080/00945710009351866

542. Li D.-M., Zhao Z.-X., Liu S.-Q. et al. Synth. Commun. 2000, 30, 4017-4026.
https://doi.org/10.1080/00397910008087017

543. Li D.-M., Zhao Z.-X., Sun H.-R. et al. Synth. React. Inorg. Met. Org. Nano-Met. Chem. 2000, 30, 1899-1915.
https://doi.org/10.1080/00945710009351877

544. Zhao Z., Liu G. Synth. React. Inorg. Met. Org. Nano-Met. Chem. 2002, 32, 465-473.
https://doi.org/10.1081/SIM-120003789

545. Wong W.-K., Hou A., Guo J. et al. J. Chem. Soc., Dalton Trans. 2001, 20, 3092-3098.
https://doi.org/10.1039/b104993n

546. Jiang F.-L., Wong W.-K., Zhu X.-J. et al. Eur. J. Inorg. Chem. 2007, 21, 3365-3374.
https://doi.org/10.1002/ejic.200700153

547. Zhu X.-J., Zhang T., Zhao S. et al. Eur. J. Inorg. Chem. 2011, 22, 3314-3320.
https://doi.org/10.1002/ejic.201100025

548. Hindre F., Plouzennec M., Certaines J. et al. J. Magn. Reson. Imaging 1993, 3, 59-65.
https://doi.org/10.1002/jmri.1880030111

549. Li G., Slansky A., Dobhal M.P., Goswami L.N. Bioconjugate Chem. 2005, 16, 32-42.
https://doi.org/10.1021/bc049807x

550. Nah M., Oh J.B., Kim H.K. et al. J. Phys. Chem. A. 2007, 111, 6157-6164.
https://doi.org/10.1021/jp0688512

551. Beeby A., Dickins R., Fitzgerald S. et al. Chem. Commun. 2000, 13, 1183-1184.
https://doi.org/10.1039/b002452j

552. Kang T.S., Harrison B.S., Foley T.J. et al. Adv. Mat. 2003, 15, 1093-1097.
https://doi.org/10.1002/adma.200304692

553. Guo L., Yan B. Inorg. Chem. Commun. 2011, 14, 1833-1837.
https://doi.org/10.1016/j.inoche.2011.08.020

554. Zhu X., Wong W.-K., Wong W.-Y., Yang X. Eur. J. Inorg. Chem. 2011, 4651-4674.
https://doi.org/10.1002/ejic.201100481

555. Mironov А.F. Russ. Chem. Rev. 2013, 82, 333-351.
https://doi.org/10.1070/RC2013v082n04ABEH004300

556. Shuhui B., Hu J., Wang Q., Liu X., Zhen Z. Photochem. Photobiol. Sci. 2008, 7, 474-479.
https://doi.org/10.1039/b715809b

557. Tolbin A., Pushkarev V., Tomilova L. Mendeleev Commun. 2008, 18, 94-95.
https://doi.org/10.1016/j.mencom.2008.03.015

558. Kasuga K., Tsutsui M. Coord. Chem. Rev. 1980, 32, 67-95.
https://doi.org/10.1016/S0010-8545(00)80370-7

559. Smola S.S., Snurnikova O.V., Fadeyev E.N. et al. Macroheterocycles 2012, 5, 343-349.
https://doi.org/10.6060/mhc2012.121193r

560. Semenishyn N.N., Smola S.S., Rusakova N.V. et al. Macroheterocycles 2017, 10, 268-272.
https://doi.org/10.6060/mhc170621r

561. Semenishyn N.N., Smola S.S., Rusakova N.V. et al. Macroheterocycles 2018, 11, 262-268.
https://doi.org/10.6060/mhc180691r

562. Gross Z., Galili N., Saltsman I. Angew. Chem. Int. Ed. 1999, 38, 1427-1429.
https://doi.org/10.1002/(SICI)1521-3773(19990517)38:10<1427::AID-ANIE1427>3.0.CO;2-1

563. Semenishyn N., Gross Z. Dalton Trans. 2013, 42, 3775-3778.
https://doi.org/10.1039/c2dt32842a

564. Buckley H.L., Anstey M.R., Gryko D.T., Arnold J. Chem. Commun. 2013, 49, 3104-3106.
https://doi.org/10.1039/c3cc38806a

565. Semenishyn N.N., Rusakova N.V. Macroheterocycles 2016, 9, 163-168.
https://doi.org/10.6060/mhc160425r

566. Day N.U., Wamser C.C., Walter M.G. Polym. Int. 2015, 64, 833-857.
https://doi.org/10.1002/pi.4908

567. Asif Mahmood et al. J. Mater. Chem. A. 2018, 6, 16769-16797.
https://doi.org/10.1039/C8TA06392C

568. Shirakawa H. et al. J. Chem. Soc., Chem. Commun. 1977, 16, 578-580.
https://doi.org/10.1039/c39770000578

569. Mac Diarmid A.G. Synthetic Metals 2001, 125(1), 11-22.
https://doi.org/10.1016/S0379-6779(01)00508-2

570. Heeger A.J. Rev. Modern Phys. 2001, 73(3), 681-700.
https://doi.org/10.1103/RevModPhys.73.681

571. Liu L., Yang D., Tian H., Ji Y. Optics Commun. 2012, 285, 171–177.
https://doi.org/10.1016/j.optcom.2011.08.066

572. Light Scattering in Solids I. Introductory Concepts (Cardona M., Ed.). Springer Berlin Heidelberg 1983. XV 366 p.
https://doi.org/10.1007/3-540-11913-2

573. Troger F. et al. Springer Berlin Heidelberg 2012, 161-251.

574. Bower D.I. Infrared Dichroism, Polarized fluorescence and Raman spectroscopy. In: Structure and Properties of Oriented Polymers (Ward I.M., Ed.). Springer Netherlands, 1997. p. 181-233.
https://doi.org/10.1007/978-94-011-5844-2

575. Sosorev A.Yu., Trukhanov V.A., Maslennikov D.R. et al. ACS Appl. Mater. Interfaces 2020, 12(8), 9507-9519.
https://doi.org/10.1021/acsami.9b20295

576. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I., Koifman O.I. Mendeleev Commun. 2019, 29, 309-311.
https://doi.org/10.1016/j.mencom.2019.05.023

577. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I. Adv. Colloid Interface Sci. 2018, 253, 23-34.
https://doi.org/10.1016/j.cis.2018.02.001

578. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I. Electrochim. Acta 2018, 292, 256-267.
https://doi.org/10.1016/j.electacta.2018.09.127

579. Chulovskaya S.A., Kuzmin S.M., Parfenyuk V.I. Macroheterocycles 2015, 8, 259-265.
https://doi.org/10.6060/mhc150662k

580. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I. J. Electroanal. Chem. 2016, 772, 80-88.
https://doi.org/10.1016/j.jelechem.2016.04.024

581. Kuzmin S.M., Chulovskaya S.A., Tesakova M.V., Semeikin A.S., Parfenyuk V.I. Macroheterocycles 2014, 7, 218-224.
https://doi.org/10.6060/mhc140511k

582. Kuzmin S.M., Chulovskaya S. A., Parfenyuk V.I. Macroheterocycles 2013, 6, 334-339.
https://doi.org/10.6060/mhc131057k

583. Tesakova M.V., Semeikin A.S., Parfenyuk V.I. J. Porphyrins Phthalocyanines 2016, 20, 793-803.
https://doi.org/10.1142/S1088424616500930

584. Kuz'min S.M., Chulovskaya S.A., Parfenyuk V.I. Russ. J. Electrochem. 2014, 50(5), 429-437.
https://doi.org/10.1134/S1023193514050073

585. Lunt R.R., Benziger J.B., Forrest S.R. Adv. Mater. 2010, 22, 1233-1236.
https://doi.org/10.1002/adma.200902827

586. Mikhnenko O.V., Lin J., Shu Y., Anthony J.R., Blom P.W.M., Nguyen T.-Q. et al. Phys. Chem. Chem. Phys. 2012, 14, 14196-14201.
https://doi.org/10.1039/c2cp41359k

587. Menke S.M., Holmes R.J. Energy Environ Sci. 2014, 7, 499-512.
https://doi.org/10.1039/C3EE42444H

588. Walter M.G., Wamser C.C. J. Phys. Chem. C. 2010, 114, 7563-7574.
https://doi.org/10.1021/jp910016h

589. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I. Electrochim. Acta 2020, 342, 136064.
https://doi.org/10.1016/j.electacta.2020.136064

590. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I., Koifman O.I. Mendeleev Commun. 2020. DOI 10.1016/j.mencom.2020.11.030.
https://doi.org/10.1016/j.mencom.2020.11.030

591. Fateeva A., Devautour-Vinot S., Heymans N., Devic T., Grenèche J.-M., Wuttke S., Miller S., Lago A., Serre C., Weireld G.D., Maurin G., Vimont A., Férey G. Chem. Mater. 2011, 23, 4641-4651.
https://doi.org/10.1021/cm2025747

592. Fateeva A., Chater P.A., Ireland C.P., Tahir A.A., Khimyak Y.Z., Wiper P.V., Darwent J.R., Rosseinsky M.J. Angew. Chem. Int. 2012, 51, 7440-7444.
https://doi.org/10.1002/anie.201202471

593. Yang X.L., Xie M.H., Zou C., He Y., Chen B., O'Keeffe M. et al. J. Am. Chem. Soc. 2012, 13, 10638-10645.
https://doi.org/10.1021/ja303728c

594. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I. J. Porphyrins Phthalocyanines 2015, 19, 1053-1062.
https://doi.org/10.1142/S1088424615500807

595. Parfenyuk V.I., Tesakova M.V., Chulovskaya S.A., Kuzmin S.M. Macroheterocycles 2019, 12, 154-164.
https://doi.org/10.6060/mhc190232p

596. Tesakova M.V., Koifman O.I., Parfenyuk V.I. J. Porphyrins Phthalocyanines 2018, 22, 632-639.
https://doi.org/10.1142/S1088424618500864

597. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I. Mater. Chem. Phys. 2020, 241, 122394.
https://doi.org/10.1016/j.matchemphys.2019.122394

598. Popov I.A., Kuzmin S.M., Chulovskaya S.A., Semeikin A.S., Parfenyuk V.I. Macroheterocycles 2012, 5(2), 131-135.
https://doi.org/10.6060/mhc2012.120254k

599. Kuzmin S.M., Chulovskaya S.A., Koifman O.I., Parfenyuk V.I. Electrochem. Commun. 2017, 83, 28-32.
https://doi.org/10.1016/j.elecom.2017.08.016

600. Tesakova M.V., Lutovac M., Parfenyuk V.I. J. Porphyrins Phthalocyanines 2018, 22, 1047-1053.
https://doi.org/10.1142/S108842461850102X

601. Kuzmin S.M., Chulovskaya S.A., Parfenyuk V.I. Electrochimica Acta 2020, 342, 136064.
https://doi.org/10.1016/j.electacta.2020.136064

601. Filimonova Yu. A., Chulovskaya S. A., Kuzmin S. M., Parfenyuk V. I. Electroplating and surface treatment. 2020, 28, 21-28 [in Russian].

602. Masa J., Ozoemena K., Schuhmann W., Zagal J.H. J. Porphyrins Phthalocyanines 2012, 16, 762-784.
https://doi.org/10.1142/S1088424612300091

603. Tryk D.A., Cabrera C.R., Fujishima A., Spataru N. In: The Electrochemical Society Proceedings (Prakash J., Chu D., Scherson D., Enayetullah M., Tae Bae I., Eds.) Pennington, New Jersey, 2005. p. 45.

604. Taylor R.J., Humffray A.A. J. Electroanal. Chem. Interfacial Electrochem. 1975, 64, 63-84.
https://doi.org/10.1016/S0022-0728(75)80278-6

605. Qin H., Xu L., Zhong D. J. Phys. Chem. C 2020, 124, 5167-5173.
https://doi.org/10.1021/acs.jpcc.9b10664

606. Hu Q., Rezaee E., Li M., Chen Q., Cao Y., Mayukh M., McGrath D.V., Xu Z.X. ACS Appl. Mater. Interfaces 2019, 11, 36535-36543.
https://doi.org/10.1021/acsami.9b09490

607. Song C., Li Y., Gao C., Zhang H., Chuai Y., Song D. Mater. Lett. 2020, 270, 127666.
https://doi.org/10.1016/j.matlet.2020.127666

608. Boileau N.T., Melville O.A., Mirka B., Cranston R., Lessard B.H. RSC Adv. 2019, 9, 2133-2142.
https://doi.org/10.1039/C8RA08829B

609. Lo P.C., Rodríguez-Morgade M.S., Pandey R.K., Ng D., Torres T., Dumoulin F. Chem. Soc. Rev. 2020, 49, 1041-1056.
https://doi.org/10.1039/C9CS00129H

610. Valli F., García Vior M.C., Roguin L.P., Marino J. Free Radic. Biol. Med. 2020, 152, 743-754.
https://doi.org/10.1016/j.freeradbiomed.2020.01.018

611. Su H.C., Tran T.T., Bosze W., Myung N.V. Sens. Actuators Reports 2020, 2, 100011.
https://doi.org/10.1016/j.snr.2020.100011

612. Wang L., Wang L., Yang G., Xie Q., Zhong S., Su X., Hou Y., Zhang B. Langmuir 2020, 36, 4532-4539.
https://doi.org/10.1021/acs.langmuir.9b03636

613. Morlanés N., Almaksoud W., Rai R.K., Ould-Chikh S., Ali M.M., Vidjayacoumar B., Al-Sabban B.E., Albahily K., Basset J.M. Catal. Sci. Technol. 2020, 10, 844-852.
https://doi.org/10.1039/C9CY02326G

614. Neamtu M., Nadejde C., Brinza L., Dragos O., Gherghel D., Paul A. Sci. Rep. 2020, 10, 1-12.
https://doi.org/10.1038/s41598-020-61980-6

615. Thomas A.L. Phthalocyanine Research and Applications. CRC Press, 1990. 304 p.

616. Terao R., Nakazono T., Parent A.R., Sakai K. Chempluschem 2016, 81, 1064-1067.
https://doi.org/10.1002/cplu.201600263

617. Filippova A., Vashurin A., Znoyko S., Kuzmin I., Razumov M., Chernova A., Shaposhnikov G., Koifman O. J. Mol. Struct. 2017, 1149, 17-26.
https://doi.org/10.1016/j.molstruc.2017.07.086

618. Vashurin A., Filippova A., Znoyko S., Voronina A., Lefedova O., Kuzmin I., Maizlish V., Koifman O. J. Porphyrins Phthalocyanines 2015, 19, 983-996.
https://doi.org/10.1142/S1088424615500753

619. Vashurin A., Kuzmin I., Razumov M., Golubchikov O., Koifman O. Macroheterocycles 2018, 11, 11-20.
https://doi.org/10.6060/mhc180168v

620. Filippova A.A., Kerner A.A., Znoiko S.A., Tikhomirova T.V., Vashurin A.S. Russ. J. Inorg. Chem. 2020, 65, 247-254.
https://doi.org/10.1134/S0036023620020047

621. Voronina A.A., Filippova A.A., Znoiko S.A., Vashurin A.S., Maizlish V.E. Russ. J. Inorg. Chem. 2015, 60, 1407-1414.
https://doi.org/10.1134/S0036023615110236

622. Reid N., Barat R. Chem. Eng. Commun. 2016, 203, 714-723.
https://doi.org/10.1080/00986445.2015.1067802

623. Saka E.T., Çağlar Y. Catal. Lett. 2017, 147, 1471-1477.
https://doi.org/10.1007/s10562-017-2054-0

624. Dai D., Yang Z., Yao Y., Chen L., Jia G., Luo L. Catal. Sci. Technol. 2017, 7, 934-942.
https://doi.org/10.1039/C6CY02317G

625. Sun X., Wang L., Tan Z. Catal. Lett. 2015, 145, 1094-1102.
https://doi.org/10.1007/s10562-015-1500-0

626. Baturhan O.E., Sağlam M.B., Özkaya A.R. Synth. Met. 2020, 263, 116351.
https://doi.org/10.1016/j.synthmet.2020.116351

627. Chen B., Bu Y., Yang J., Nian W., Hao S. Chem. Eng. J. 2020, 399, 125675.
https://doi.org/10.1016/j.cej.2020.125675

628. Li L., Wu H., Chen H., Zhang J., Xu X., Wang S., Wang S., Sun H. Chemosphere 2020, 256, 127160.
https://doi.org/10.1016/j.chemosphere.2020.127160

629. Wang C., Shao N., Xu J., Zhang Z., Cai Z. J. Hazard. Mater. 2020, 388, 121751.
https://doi.org/10.1016/j.jhazmat.2019.121751

630. Gong J., Li D., Huang J., Ding L., Tong Y., Li K., Zhang C. Catal. Lett. 2014, 144, 487-497.
https://doi.org/10.1007/s10562-013-1178-0

631. Vashurin A., Kuzmin I., Mayzlish V., Razumov M., Golubchikov O., Koifman O. J. Serbian Chem. Soc. 2016, 81, 1025-1036.
https://doi.org/10.2298/JSC160105048V

632. Vashurin A., Maizlish V., Pukhovskaya S., Voronina A., Kuzmin I., Futerman N., Golubchikov O., Koifman O. J. Porphyrins Phthalocyanines 2015, 19, 573-581.
https://doi.org/10.1142/S1088424614501028

633. Tugba S.E., Tekintas K. J. Mol. Struct. 2020, 1215, 128189.
https://doi.org/10.1016/j.molstruc.2020.128189

634. Vashurin A., Erzunov D., Kazaryan K., Tonkova S., Tikhomirova T., Filippova A., Koifman O. Dyes and Pigments 2020, 174, 108018.
https://doi.org/10.1016/j.dyepig.2019.108018

635. Makarov S.G., Ketkov S.Y.,Wöhrle D. Chem. Commun. 2020, 56, 5653-5656.
https://doi.org/10.1039/D0CC01653E

636. Vashurin A., Marfin Y., Tarasyuk I., Kuzmin I., Znoyko S., Goncharenko A., Rumyantsev E. Appl. Organomet. Chem. 2018, 32, e4482.
https://doi.org/10.1002/aoc.4482

637. Vashurin A.S. Russ. Chem. Bull. 2016, 65, 2220-2228.
https://doi.org/10.1007/s11172-016-1572-z

638. Tripathi D., Negi H., Singh R.K., Singh U.P., Srivastava V.C. J. Coord. Chem. 2019, 72, 2982-2996.
https://doi.org/10.1080/00958972.2019.1683549

639. Yang Y., Li M., Ren Y., Li Y., Xia C. Int. J. Hydrogen Energy 2018, 43, 3797-3802.
https://doi.org/10.1016/j.ijhydene.2017.12.183

640. Thiruppathiraja T., Arokiyanathan A., Aazaad B., Silviya R., Lakshmipathi S. Int. J. Hydrogen Energy 2020, 45, 8540-8548.
https://doi.org/10.1016/j.ijhydene.2020.01.079

641. Guo S., Li D., Gao B., Li Y., Zhang H., Li Y., Duan Q. J. Coord. Chem. 2019, 72, 1146-1155.
https://doi.org/10.1080/00958972.2019.1578878

642. Huai M., Yin Z., Wei F., Wang G., Lu J., Zhuang L. Chem. Phys. Lett. 2020, 754, 137655.
https://doi.org/10.1016/j.cplett.2020.137655

643. Ma D.D., Han S.G., Cao C., Li X., Wu X.T., Zhu Q.L. Appl. Catal. B Environ. 2020, 264, 118530.
https://doi.org/10.1016/j.apcatb.2019.118530

644. Li K., Zhu J., Liu Q., Li Z., Zhao J. J. Electrochem. Soc. 2020, 167, 040506.
https://doi.org/10.1149/1945-7111/ab7184

645. Silva N., Castro-Castillo C., Oyarzún M., Ramírez S., Gutierrez-Ceron C., Marco J., Silva J., Zagal J. Electrochim. Acta 2019, 308, 295-306.
https://doi.org/10.1016/j.electacta.2019.04.005

646. Yan X., Xu X., Liu Q., Guo J., Kang L., Yao J. J. Power Sources 2018, 389, 260-266.
https://doi.org/10.1016/j.jpowsour.2018.03.042

647. Mahmiani Y., Sevim A., Gül A. J. Photochem. Photobiol. A Chem. 2016, 321, 24-32.
https://doi.org/10.1016/j.jphotochem.2015.12.015

648. Koç Keşir M., Dilber G., Sökmen M., Durmuş M. J. Sol-Gel Sci. Technol. 2020, 93, 687-694.
https://doi.org/10.1007/s10971-019-05109-w

649. Zhou Z., Chen A., Kong A., Fan X., Zhang X., Shan Y. J. Electrochem. Soc. 2018, 165, H658-H666.
https://doi.org/10.1149/2.1131810jes

650. Qian M., Ma J., Materials M. Trans. Tech. Publ. 2017, 748, 433-437.
https://doi.org/10.4028/www.scientific.net/KEM.748.433

651. Wang R., Liu Y., Zuo P., Zhang Z., Lei ., Liu Y. Environ. Sci. Pollut. Res. 2020, 27, 18831-18842.
https://doi.org/10.1007/s11356-020-08425-9

652. Huang Y., Yang Z., Yang S., Xu Y. J. Adv. Nanomater. 2017, 2, 146-153.
https://doi.org/10.1016/B978-0-12-849903-0.00008-7

653. Chauhan P., Yan N. RSC Adv. 2015, 5, 37517-37520.
https://doi.org/10.1039/C4RA16869K

654. Ziyadova T.M., Burmistrov V.A., Maizlish V.E., Koifman O.I. Russ. J. Phys. Chem A 2017, 91, 460-463.
https://doi.org/10.1134/S0036024417030323

655. Ziyadova T.M., Burmistrov V.A., Maizlish V.E., Koifman O.I. Kinet. Catal. 2016, 57, 313-318.
https://doi.org/10.1134/S0023158416030186

656. Mapukata S., Kobayashi N., Kimura M., Nyokong T. J. Photochem. Photobiol. A Chem. 2019, 379, 112-122.
https://doi.org/10.1016/j.jphotochem.2019.04.048

657. Zhu Z., Chen Y., Gu Y., Wu F., Lu W., Xu T., Chen W. Water Res. 2016, 93, 296-305.
https://doi.org/10.1016/j.watres.2016.02.035

658. Bridwell-Rabb J., Drennan C.L. Curr. Opin. Chem. Biol. 2017, 37, 63-70.
https://doi.org/10.1016/j.cbpa.2017.01.013

659. Giedyk M., Goliszewska K., Gryko D. Chem. Soc. Rev. 2015, 44, 3391-3404.
https://doi.org/10.1039/C5CS00165J

660. Zelder F. Chem. Commun. 2015, 51, 14004-14017.
https://doi.org/10.1039/C5CC04843E

661. Lexa D., Saveant J.-M. Acc. Chem. Res. 1983, 16, 235-243.
https://doi.org/10.1021/ar00091a001

662. Dereven'kov I.A., Hannibal L., Dürr M., Salnikov D.S., Bui Thi T.T., Makarov S.V., Koifman O.I., Ivanović-Burmazović I. J. Organomet. Chem. 2017, 839, 53-59.
https://doi.org/10.1016/j.jorganchem.2017.01.002

663. Dereven'kov I.A., Bui Thi T.T., Salnikov D.S., Makarov S.V. Russ. J. Phys. Chem. A 2016, 90, 596-600.
https://doi.org/10.1134/S0036024416030080

664. Lexa D., Saveant J.M., Zickler J. J. Am. Chem. Soc. 1980, 102, 2654-2663.
https://doi.org/10.1021/ja00528a023

665. Birke R.L., Huang Q., Spataru T., Gosser D.K. Jr. J. Am. Chem. Soc. 2006, 128, 1922-1936.
https://doi.org/10.1021/ja054479c

666. Sajan A., Birke R.L. Electroanalysis 2016, 28, 2743-2753.
https://doi.org/10.1002/elan.201600341

667. Dereven'kov I.A., Makarov S.V., Bui Thi T.T., Makarova A.S., Koifman O.I. Eur. J. Inorg. Chem. 2018, 2987-2992.
https://doi.org/10.1002/ejic.201800066

668. Pallares I.G., Moore T.C., Escalante-Semerena J.C., Brunold T.C. J. Am. Chem. Soc. 2016, 138, 3694-3704.
https://doi.org/10.1021/jacs.5b11708

669. Dürichen H, Diekert G, Studenik S. Protein Sci. 2019, 28, 1902-1908.
https://doi.org/10.1002/pro.3699

670. Johnston R.C., Zhou J., Smith J.C., Parks J.M. J. Phys. Chem. A 2016, 120, 7307-7318.
https://doi.org/10.1021/acs.jpcb.6b02701

671. Kumar M., Hirao H., Kozlowski P.M. J. Biol. Inorg. Chem. 2012, 17, 1107-1121.
https://doi.org/10.1007/s00775-012-0924-x

672. Kumar M., Kozlowski P.M. Angew. Chem. Int. Ed. 2011, 50, 8702-8705.
https://doi.org/10.1002/anie.201100469

673. Bhat S.A., Rashid N., Rather M.A., Pandit S.A., Ingole P.P., Bhat M.A. Electrochim. Acta 2020, 337, article number 135730
https://doi.org/10.1016/j.electacta.2020.135730

674. Robertson W.D., Bovell A.M., Warncke K. J. Biol. Inorg. Chem. 2013, 18, 701-713.
https://doi.org/10.1007/s00775-013-1015-3

675. Lexa D., Savéant J.-M. J. Chem. Soc., Chem. Commun. 1975, 872-874.
https://doi.org/10.1039/C39750000872

676. Shimakoshi H., Hisaeda Y. ChemPlusChem 2014, 79, 1250-1253.
https://doi.org/10.1002/cplu.201402081

677. Tian H., Shimakoshi H., Imamura K., Shiota Y., Yoshizawa K., Hisaeda Y. Chem. Commun. 2017, 53, 9478-9481.
https://doi.org/10.1039/C7CC04377E

678. Shimakoshi H., Luo Z., Tomita K., Hisaeda Y. J. Organomet. Chem. 2017, 839, 71-77.
https://doi.org/10.1016/j.jorganchem.2017.02.002

679. Ogawa A., Oohora K., Hayashi T. Inorg. Chem. 2018, 57, 14644-14652.
https://doi.org/10.1021/acs.inorgchem.8b02333

680. Grodkowski J., Neta P. J. Phys. Chem. A 2000, 104, 1848-1853.
https://doi.org/10.1021/jp9939569

681. Wang Y., Chen Z. Talanta 2010, 82, 534-539.
https://doi.org/10.1016/j.talanta.2010.05.020

682. Ji J., Chung Y., Kwon Y. J. Mat. Chem. C 2020, 8, 2749-2755.
https://doi.org/10.1039/C9TC06345E

683. Shahadat H.M., Younus H.A., Ahmad N., Shiguo Z., Zhuiykov S., Verpoort F. Chem. Commun. 2020, 56, 1968-1971.
https://doi.org/10.1039/C9CC08838E

684. Shimakoshi H., Hisaeda Y. Curr. Opin. Electrochem. 2018, 8, 24-30.
https://doi.org/10.1016/j.coelec.2017.12.001

685. Tahara K., Pan L., Ono T., Hisaeda Y. Beilstein J. Org. Chem. 2018, 14, 2553-2567.
https://doi.org/10.3762/bjoc.14.232

686. Thordarson P. Chem. Soc. Rev. 2011, 40, 1305-1323.
https://doi.org/10.1039/C0CS00062K

687. Zaitseva S.V., Zdanovich S.A., Koifman O.I. Macroheterocycles 2012, 5, 81-86.
https://doi.org/10.6060/mhc2012.111149z

688. Iwamoto H., Nishi S., Haino T. Chem. Commun. 2011, 47, 12670-12672.
https://doi.org/10.1039/c1cc14739k

689. Kundrat O., Kas M., Tkadlecova M., Lang K., Cvacka J., Stibor I., Lhotak P. Tetrahedron Lett. 2007, 48, 6620-6623.
https://doi.org/10.1016/j.tetlet.2007.07.137

690. Sallas F., Darcy R. Eur. J. Org. Chem. 2008, 6, 957-969.
https://doi.org/10.1002/ejoc.200700933

691. Korendovych I.V., Roesner R.A., Rybak-Akimova E.V. Adv. Inorg. Chem. 2007, 59, 109-173.
https://doi.org/10.1016/S0898-8838(06)59004-X

692. Puglisi A., Purrello R., Rizzarelli E., Sortino S., Vecchio G. New J. Chem. 2007, 31, 1499-1506.
https://doi.org/10.1039/b703680a

693. Hosokawa K., Miura Y., Kiba T., Kakuchi T., Sato S. Chem. Lett. 2008, 37, 60-61.
https://doi.org/10.1246/cl.2008.60

694. Fathalla M., Li S., Diebold U., Alb A., Jayawickramarajah J. Chem. Commun. 2009, 4209-4211.
https://doi.org/10.1039/b908050c

695. Kralova J., Kejik Z., Briza T., Pouckova P., Kral A., Martasek P., Kral V. J. Med. Chem. 2010, 53, 128-138.
https://doi.org/10.1021/jm9007278

696. Guo Y., Zhang P., Chao J., Shuang S., Dong C. Spectrochim. Acta A 2008, 71A, 946-950.
https://doi.org/10.1016/j.saa.2008.02.018

697. Fathalla M., Neuberger A., Li S.-C., Schmehl R., Diebold U., Jayawickramarajah J. J. Am. Chem. Soc. 2010, 132, 9966-9967.
https://doi.org/10.1021/ja1030722

698. Guo Y.-J., Chao J.-B., Pan J.-H. Spectrochim. Acta A 2007, 68A, 231-236.
https://doi.org/10.1016/j.saa.2006.11.019

699. Kiba T., Suzuki H., Hosokawa K., Kobayashi H., Baba S., Kakuchi T., Sato S. J. Phys. Chem. B 2009, 113, 11560-11563.
https://doi.org/10.1021/jp905904h

700. Ermilov E.A., Menting R., Lau J.T.F., Leng X., Roeder B., Ng D.K.P. Phys. Chem. Chem. Phys. 2011, 13, 17633-17641.
https://doi.org/10.1039/c1cp21930h

701. Samaroo D., Vinodu M., Chen X., Drain C.M. J. Comb. Chem. 2007, 9, 998-1011.
https://doi.org/10.1021/cc070067j

702. Tsuda A. Bull. Chem. Soc. Jpn. 2009, 82, 11-28.
https://doi.org/10.1246/bcsj.82.11

703. Goldberg I. CrystEngComm 2008, 10, 637-645.
https://doi.org/10.1039/b800107c

704. Boyd P.D.W., Reed C.A. Acc. Chem. Res. 2005, 38, 235-242.
https://doi.org/10.1021/ar040168f

705. Jurow M., Schuckman A.E., Batteas J.D., Drain C.M. Coord. Chem. Rev. 2010, 254, 2297-2310.
https://doi.org/10.1016/j.ccr.2010.05.014

706. Chen Y., Zhang Y., Liu Y. Isr. J. Chem. 2011, 51, 515-524.
https://doi.org/10.1002/ijch.201100010

707. Endo T. Chem. Rec. 2011, 11, 146-157.
https://doi.org/10.1002/tcr.201100001

708. Kraus T. Curr. Org. Chem. 2011, 15, 802-814.
https://doi.org/10.2174/138527211794518907

709. De Rossi R.H., Silva O.F., Vico R.V., Gonzalez C.J. Pure Appl. Chem. 2009, 81, 755-765.
https://doi.org/10.1351/PAC-CON-08-08-13

710. Ballester P., Claudel M., Durot S., Kocher L., Schoepff L., Heitz V. Chem. Eur. J. 2015, 21, 15339-15348.
https://doi.org/10.1002/chem.201502152

711. Maufroy A., Favereau L., Anne F.B., Pellegrin Y., Blart E., Hissler M., Jacquemin D., Odobel F. J. Mater. Chem. A 2015, 3, 3908-3917.
https://doi.org/10.1039/C4TA05974C

712. Koifman O.I., Mamardashvili N.Z., Antipon I.S. Synthetic Receptors on the Base of Porphyrins and Their Conjugates with Calix[4]arenes (Konovalov A.I., Ed.) Moscow, 2006. 248 p.

713. Mamardashvili G.M., Zvezdina S.V., Mamardashvili N.Z. Russ. J. Gen. Chem. 2011, 81, 594-601.
https://doi.org/10.1134/S1070363211030273

714. Kulikova O.M., Mamardashvili N.Z. Russ. J. Org. Chem. 2010, 46(8), 1244-1248.
https://doi.org/10.1134/S107042801008021X

715. Rossom W.V., Kundrat O., Ngo T.H., Lhotak P., Dehaen W., Maes W. Tetrahedron Lett. 2010, 51, 2423-2426.
https://doi.org/10.1016/j.tetlet.2010.02.137

716. Nakazawa J., Mizuki M., Shimazaki Y., Tani F., Naruta Y. Org. Lett. 2006, 8, 4275-4278.
https://doi.org/10.1021/ol061561j

717. Durot S., Taesch J., Heitz V. Chem. Rev. 2014, 114, 8542-8578.
https://doi.org/10.1021/cr400673y

718. Qiu W.-G., Li Z.-F., Bai G.-M., Meng S.-N., Dai H.-X., He H. Spectrochim. Acta A 2007, 66A, 1189-1193.
https://doi.org/10.1016/j.saa.2006.06.006

719. Guo Y.-J., Guo L., Pan J.-H. Phys. Chem. Liq. 2007, 45, 261-269.
https://doi.org/10.1080/00319100601137213

720. Tsuchiya Y., Yamano A., Shiraki T., Sada K., Shinkai S. Chem. Lett. 2011, 40, 99-101.
https://doi.org/10.1246/cl.2011.99

721. Callari F.L., Mazzaglia A., Scolaro L.M., Valli L., Sortino S. J. Mater. Chem. 2008, 18, 802-805.
https://doi.org/10.1039/b717260e

722. Yu M., Chen Y., Zhang N., Liu Y. Org. Biomol. Chem. 2010, 8, 4148-4154.
https://doi.org/10.1039/c0ob00080a

723. Favereau L., Warnan J., Anne F.B., Pellegrin Y., Blart E., Jacquemin D., Odobel F. J. Mater. Chem. A 2013, 1, 7572-7575.
https://doi.org/10.1039/c3ta11380a

724. Bichan N.G., Tyulyaeva E.Yu., Khodov I.A., Lomova T.N. J. Mol. Struct. 2014, 1061, 82-89.
https://doi.org/10.1016/j.molstruc.2013.12.074

725. Nguyen N.T., Mamardashvili G.M., Kulikova O.M., Scheblykin I.G., Mamardashvili N.Z., Dehaen W. RSC Adv. 2014, 4, 19703-19709.
https://doi.org/10.1039/C3RA45660A

726. Albrecht K., Kasai Y., Kimoto A., Yamamoto K. Macromolecules 2008, 41, 3793-3800.
https://doi.org/10.1021/ma800265h

727. Albrecht K., Kasai Y., Kuramoto Y., Yamamoto K. Chem. Comun. 2013, 46, 6861-6863.
https://doi.org/10.1039/c3cc43249a

728. Wang L., Li H., Deng J., Cao D. Curr. Org. Chem. 2013, 17, 3078-3091.
https://doi.org/10.2174/13852728113179990024

729. Su S., Ding Y., Li Y., Wu Y., Nie G. Biomaterials 2016, 80, 169-178.
https://doi.org/10.1016/j.biomaterials.2015.11.058

730. Tsolekile N., Nelana S., Oluwafemi O.S. Molecules 2019, 249140, 2669.
https://doi.org/10.3390/molecules24142669

731. Mamardashvili N., Maltseva O., Ivanova Y., Mamardashvili G. Tetrahedron Lett. 2008, 49, 3752-3756.
https://doi.org/10.1016/j.tetlet.2008.04.029

732. Paolesse R., Monti D., Nardis S., Di Natale C., Porphyrin-Based Chemical Sensors In: Handbook of Porphyrin Science (Kadish K.M., Smith K.M., Guilard R., Eds.) World Scientific Publishing Co., 2013. p. 121-215.
https://doi.org/10.1002/chin.201311276

733. Cioates C., Van Staden S.- R., Van Staden F. J. Solid State Sci. Techn. 2020, 9, 051005.
https://doi.org/10.1149/2162-8777/ab9a5d

734. Gottfried M. J. Surf. Sci. Rep. 2015, 70, 259-379.
https://doi.org/10.1016/j.surfrep.2015.04.001

735. Fagadar-Cosma G., Birdeanu M., Fagadar-Cosma E. J. Res. Updates in Polym. Sci. 2016, 5, 39-51.
https://doi.org/10.6000/1929-5995.2016.05.01.4

736. Rodriguez-Mendez M., Antoniode de Saja J. Molecular Materials for Gas Sensor and Sensor Arrays. In: Adv. Nanomat. Inexpens. Gas Microsen. (Elsevier B.V., Liobet E., Eds.) 2020. p. 37-54.
https://doi.org/10.1016/B978-0-12-814827-3.00003-7

737. Paolesse R., Nardis S., Monti D., Stefanelli M., Di Natale C. Chem. Rev. 2017, 117, 2517−2583.
https://doi.org/10.1021/acs.chemrev.6b00361

738. Gouterman M. Optical Spectra and Electronic Structure of Porphyrins and Related Rings. In: The Porphyrins. (Dolphin D., Ed.) New York: Academic, 1978. p. 1-128.
https://doi.org/10.1016/B978-0-12-220103-5.50008-8

739. Di Amico A., Di Natale C., Paolesse R., Macagnano A., Mantini A. Sens. Actuators 2000, B65, 209-215.
https://doi.org/10.1016/S0925-4005(99)00342-1

740. Rivera M., Rivera J. M., Amelines-Sarria O., Wang Y. A. Adv. Mater. Phys. Chem. 2018, 8, 441-457.
https://doi.org/10.4236/ampc.2018.811030

741. Celiesiute R., Ramanaviciene A., Gicevicius M., Ramanavicius A. Critical Rev. Anal. Chem. 2018, 49, 195–208.
https://doi.org/10.1080/10408347.2018.1499009

742. Supriya S., Shetti V. S., Hegde G. New J. Chem. 2018, 42, 12328-12348.
https://doi.org/10.1039/c8nj02254b

743. Itagaki Y., Deki K., Nakashima S-I., Sadaoka Y. Sens. Actuat. B Chem. 2005, 108, 393-397.
https://doi.org/10.1016/j.snb.2004.10.055

744. Ma X., Sun J., Wang M., Hu M., Chen G.H., Huang J. Sens. Actuat. B 2006, 114, 1035-1042.
https://doi.org/10.1016/j.snb.2005.07.073

745. Korposh S.O., Takahara N., Ramsden J.J., Lee S.-W., Kunitake T. J. Biol. Phys. Chem. 2006, 6, 125-132.

746. Muthukumar P., John S.A. Sens. Actuat., B 2011, 159, 238−244.
https://doi.org/10.1016/j.snb.2011.06.079

747. Kalimuthu P., Sivanesan A., John S.A. J. Chem. Sci. 2012, 124, 1315-1325.
https://doi.org/10.1007/s12039-012-0330-5

748. Cano M., Castillero P., Roale J., Pedrosa J.M., Brittle S., Richardson T., González-Elipe A.R., Barranco A. Sensor. Actuat. B Chem. 2010, 150, 764-769.
https://doi.org/10.1016/j.snb.2010.07.059

749. Lv Y., Wu J., Xu Z.K. Sensor. Actuat. B-Chem. 2010, 148, 233-239.
https://doi.org/10.1016/j.snb.2010.05.029

750. Lin F.-W., Xu X.-L., Wan L.-S., Wu J., Xu Z.K. RSC Adv. 2015, 5, 30472−30477.
https://doi.org/10.1039/C5RA01605C

751. Hu M., Kang W., Cheng B., Li Z., Zhao Y., Li L. Microchem. Acta 2016, 183(5), 1713-1720.
https://doi.org/10.1007/s00604-016-1801-z

752. Hu M., Kang W., Zhao Y., Shia J., Cheng B. RSC Adv. 2017, 7, 26849-26856.
https://doi.org/10.1039/C7RA02040F

753. Hu M., Kang W., Zhong Z., Cheng B., Xing W. Ind. Eng. Chem. Res. 2018, 57(34), 11668-11674.
https://doi.org/10.1021/acs.iecr.8b02902

754. Wang B., Chen Z., Zuo X., Wu Y., He C., Wang X., Li Z. Sensor. Actuat., B-Chem. 2011, 160, 1-6.
https://doi.org/10.1016/j.snb.2011.06.049

755. Muthukumar P., John S.A. Sensor. Actuat. B-Chem. 2012, 174, 74-80.
https://doi.org/10.1016/j.snb.2012.08.022

756. Castillero P., Roales J., Lopes-Costa T., Sanchez-Valencia J.R., Barranco A., Gonzalez-Elipe A.R., Pedrosa J.M. Sensors 2017, 17, 24-38.
https://doi.org/10.3390/s17010024

757. Kim J., Lim S.-H., Yoon Y., Thangadurai T.D., Yoon S. Tetrahedron Lett. 2011, 52, 2645-2648.
https://doi.org/10.1016/j.tetlet.2011.03.048

758. Korposh S., James S.W., Lee S.-W., Topliss S.M., Cheung S.C., Batty W.J., Tatam R.P. Opt. Express 2010, 18, 13227-13238.
https://doi.org/10.1364/OE.18.013227

759. Jarzebinska R., Korposh S., James S., Batty W., Tatam R., Lee S.-W. Anal. Lett. 2012, 45(10), 1297-1309.
https://doi.org/10.1080/00032719.2012.673097

760. Wang T., Korposh S., James S.W., Tatam R. P., Lee S-W. Sens. Actuators, B 2016, 228, 573-580.
https://doi.org/10.1016/j.snb.2016.01.058

761. Korposh S., Kodaira S., Selyanchyn R., Ledezma F.H., James S.W., Lee S.-W. Opt. Laser Tech. 2018, 101, 1-10.
https://doi.org/10.1016/j.optlastec.2017.10.027

762. Sawada K., Tanaka T., Yokoyama T., Yamachi R., Oka Y., Masai H., Terao J., Uchida K. Jpn. J. Appl. Phys. 2020, 59, 1-6.
https://doi.org/10.35848/1347-4065/ab6b80

763. Richardson T.H., Brook R.A., Davis F., Hunter C.A. Coll. Sur. A: Physicochem. Eng. Aspects 2006, 284-285, 320-325.
https://doi.org/10.1016/j.colsurfa.2005.11.076

764. Roales J., Pedrosa J.M., Castillero P., Cano M., Richardson T.H. Thin Solid Films 2011, 519, 2025−2030.
https://doi.org/10.1016/j.tsf.2010.10.038

765. Roales J., Pedrosa J.M., Guillen M.G., Lopes-Costa T., Castillero P., Barranco A., González-Elipe A.R. Sensors 2015, 15, 11118-11132.
https://doi.org/10.3390/s150511118

766. Mc Donagh C., Burke C.S., Mc Craith B.D. Chem. Rev. 2008, 108, 400−422.
https://doi.org/10.1021/cr068102g

767. Peter C., Schmitt K., Apitz M., Woellenstein J. Microsyst. Technol. 2012, 18, 925-930.
https://doi.org/10.1007/s00542-011-1412-x

768. Abudukeremu H., Kari N., Zhang Y., Wang J., Nizamidin P., Abliz S., Yimit A. J. Mater. Sci. 2018, 53, 10822-10834.
https://doi.org/10.1007/s10853-018-2374-5

769. Kutilike B., Kari N., Zhang Y., Nizamidin P., Yimit A. Meas. Sci. Technol. 2020, 31, 055105.
https://doi.org/10.1088/1361-6501/ab6e24

770. Diab N., Schuhmann W. Electrochim. Acta 2001, 47, 265-273.
https://doi.org/10.1016/S0013-4686(01)00565-5

771. Miki H., Matsubara F., Nakashima S., Ochi S., Nakagawa K., Matsuguchi M., Sadaoka Y. Sens. Actuat. 2016, 231, 458-468.
https://doi.org/10.1016/j.snb.2016.02.145

772. Shiba S., Yamada K., Matsuguchi M. Sensors 2020, 20, 1295.
https://doi.org/10.3390/s20051295

773. Khan A.H., Rao M.V., Li Q. Sensors 2019, 19(905), 1-39.
https://doi.org/10.3390/s19040905

774. Strianese M., Lamberti M., Pellecchi C. Dalton Trans. 2017, 46, 1872-1879.
https://doi.org/10.1039/C6DT04753J

775. Vikrant K., Kumar V., Ok Y., Kim K., Deep A. Trends Anal. Chem. 2018, 105, 263-281.
https://doi.org/10.1016/j.trac.2018.05.013

776. Chen J., Zhu Y., Kaskel S. Angew. Chem. Int. Ed. 2020.
https://doi.org/10.1002/anie.201909880

777. Ma Y., Su H., Kuang X., Li X., Zhang T., Tang, B. Anal. Chem. 2014, 86(22), 11459-11463.
https://doi.org/10.1021/ac503622n

778. Tuerdi G., Kari N., Yan Y., Nizamidin P., Yimit A. Sensors 2017, 17(12), 2717. doi:10.3390/s17122717.
https://doi.org/10.3390/s17122717

779. Mamtmin G., Kari N., Abdurahman R., Nizamidin P., Yimit A. Opt. Las. Tech. 2020, 128, 106260.
https://doi.org/10.1016/j.optlastec.2020.106260

780. Maimaiti A., Abdurahman R., Kari N., Ma Q., Wumaier K., Nizamidin P., Yimit A. J. Modern Opt. 2020, 67(6), 507-514.
https://doi.org/10.1080/09500340.2020.1758817

781. Amao Y., Okura I. J. Porphyrins Phthalocyanines 2009, 13, 1111-1122.
https://doi.org/10.1142/S1088424609001455

782. Hutter L.H., Muller B.J., Koren K., Borisov S.M., Klimant I. J. Mater. Chem. C 2014, 2, 7589-7598.
https://doi.org/10.1039/C4TC00983E

783. Kimura T., Watanabe S., Sawada S., Shibasaki Y., Oishi Y. J. Polym. Sci., A: Pol. Chem. 2017, 55, 1086-1094.
https://doi.org/10.1002/pola.28469

784. Arunkumar C., Kooriyaden F. R., Zhang X., Sujatha S., Zhao J. New J. Chem. 2017, 41, 4908-4917.
https://doi.org/10.1039/C7NJ01141E

785. Biring S., Sadhu A.S., Deb M. Sensors 2019, 19, 5124.
https://doi.org/10.3390/s19235124

786. Mao Y., Gao Y., Wu S., Wu S., Shi J., Zhou B., Tian Y. Sens. Actuat. B: Chem. 2017, 251, 495-502.
https://doi.org/10.1016/j.snb.2017.05.081

787. Mao Y., Mei Z., Wen J., Li G., Tian Y., Zhou B., Tian Y. Sens. Actuat. 2018, B257, 944-953.
https://doi.org/10.1016/j.snb.2017.11.042

788. Mao Y., Akram M., Shi J., Wen J., Yang C., Jiang J., Zhou B., Tian Y. Sens. Actuat. B: Chem. 2019, 282, 885-895.
https://doi.org/10.1016/j.snb.2018.11.143

789. Spencer J.A., Ferraro F., Roussakis E., Klein A., Wu J., Runnels J.M., Zaher W., Mortensen L.J., Alt C., Turcotte R., Yusuf R., Cote D., Vinogradov S.A., Scadden D.T., Lin C.P. Nature 2014, 508, 269-273.
https://doi.org/10.1038/nature13034

790. The Porphyrin Handbook. Biochemistry and Binding: Activation of Small Molecules. Vol. 4. (Kadish K.M., Smith K.M., Guilard R., Eds.) New York: Academ. Press, 2000. 341 p.

791. Porphyrins: Spectroscopy, Electrochemistry, Applications. (Enikolopyan N.S., Ed.) Moscow: Nauka, 1987. 384 p.

792. Mamardashvili G.M., Mamardashvili N.Zh., Koifman O.I. Russ. Chem. Rev. 2005, 74(8), 765-780.
https://doi.org/10.1070/RC2005v074n08ABEH001056

793. Zaitsev S.Yu. Supramolecular Nanoscale Systems at the Interface of the Phases. Concepts and Perspectives for Bionanotechnologies. М.: LENAND, 2010. 212 p.

794. Kitzerow H-S, Bahr C. Chirality in Liquid Crystals. New York (NY): Springer-Verlag Inc, 2001.
https://doi.org/10.1007/b97374

795. Kelly S.M., O'Neill M. Liquid Crystals for Electro-Optic Applications. In: Handbook of Advanced Electronic and Photonic Materials and Devices Vol. 7: Liquid Crystals, Display and Laser Materials. (Nalwa H.S., Ed.) N.Y. etc.: Academic Press, 2000. p. 1-66.
https://doi.org/10.1016/B978-012513745-4/50057-3

796. Onuchak L.A., Arutunov J.I., Kuraeva J.G., et.al. Method for Analysis of Structural and Optical Isomers, 2014, Patent RF No RU 2528126.

797. Matt B., Pondman K.M., Asshoff S.J., et al. Angew. Chem. Int. Edit. 2014, 53, 12446.
https://doi.org/10.1002/anie.201404312

798. Eelkema R. Liq. Cryst. 2011, 38, 1641-1652.
https://doi.org/10.1080/02678292.2011.600779

799. Cachelin P., Green J.P., Peijs T., Heeney M., Bastiaansen W.M. Adv. Opt. Mater. 2016, 4, 592-596.
https://doi.org/10.1002/adom.201500549

800. Iwan A., Boharewicz B., Tazbir I., Hamplová V., Bubnov A. Solid-State Electronics 2015, 104, 53-60.
https://doi.org/10.1016/j.sse.2014.11.010

801. Ishida Y., Kai Y., Kato S., et al. Angew. Chem. Int. Edit. 2008, 47, 8241-8245.
https://doi.org/10.1002/anie.200803242

802. Van Delden R.A., Koumura N., Harada N., Feringa B.L. PNAS. 2002, 99, 4945-4949.
https://doi.org/10.1073/pnas.062660699

803. Gottarelli G., Spada G.P. Mol. Cryst. Liq. Cryst. 1985, 123(1), 377-388.
https://doi.org/10.1080/00268948508074792

804. Celebre G., de Luca G., Maiorino M., et al. J. Amer. Chem. Soc. 2005, 127, 11736-11744.
https://doi.org/10.1021/ja051589a

805. Watanabe G., Yoshida J. J. Phys. Chem. B 2016, 120, 6858-6864.
https://doi.org/10.1021/acs.jpcb.6b04669

806. Yoshida J., Watanabe G., Kakizawa K., et al. Inorg. Chem. 2013, 52, 11042-11050.
https://doi.org/10.1021/ic401240f

807. Engelmann M., Braun M., Kuball H‐G. Liq. Cryst. 2007, 34, 73-77.
https://doi.org/10.1080/02678290601061496

808. Braun M., Hahn A., Engelmann M., et al. Chem. Eur. J. 2005, 11, 3405-3412.
https://doi.org/10.1002/chem.200401292

809. Handbook of Porphyrin Science with Applications to Chemistry, Physics, Materials Science, Engineering, Biology and Medicine.Vol. 7. Physicochemical Characterization. (Kadish K.M., Smith K.M., Guilard R., Eds.) World Scientific Publishing: Co. Pte. Ltd., 2010.

810. Kobayashi N. Optically Active Porphyrin Systems Analyzed by Circular Dichroism. In: Handbook of Porphyrin Science. Vol. 7. Ch. 33. (Kadish K.M., Smith K.M., Guilard R., Eds.) Singapore: World Scientiﬁc, 2010. p.147−240.
https://doi.org/10.1142/9789814307246_0005

811. Lu H., Kobayashi N. Chem Rev. 2016, 116, 6184-6261.
https://doi.org/10.1021/acs.chemrev.5b00588

812. Lehmann M., Dechant M., Gerbig L., et al. Liq. Cryst. 2019, 46, 1985-1994.
https://doi.org/10.1080/02678292.2019.1618936

813. Burmistrov V.A., Novikov I.V., Aleksandriiskii V.V., et al. J. Mol. Liq. 2019, 287, 110961.
https://doi.org/10.1016/j.molliq.2019.110961

814. Burmistrov V.A., Novikov I.V., Alexandriiskii V.V., Semeikin A.S., Koifman O.I. Liq. Cryst. 2020. DOI:10.1080/02678292.2020.1817583.
https://doi.org/10.1080/02678292.2020.1817583

815. Davankov V.A. Ligand Exchange Chromatography. Encyclopedia of Separation Science.Vol. 5. (Wilson I.D., Adlard E.R., Cooke M., Pool C.F., Eds.) Amsterdam: Acad.Press, 2000. p. 2369-2380.
https://doi.org/10.1016/B0-12-226770-2/03111-2

816. Davankov V., Navratil J., Walton H. Ligand Exchange Chromatography. USA: SRC-Press, 1988. 209 p.

817. Wenzel T.J., Yarmaloff L.W., St.Cyr L.Y., O'Meara L.J., Donatelli M., Bauer R.W. J. Chromatogr. 1987, 396, 51-64.
https://doi.org/10.1016/S0021-9673(01)94042-7

818. Burmistrov V.A., Rodicheva J.A., Trifonova I.P., Koifman O.I. Modern Tendencies in Materials Functionalization by Macroheterocycles. In: Functional Materials Based on Tetrapyrrole Macrocyclic Compounds. Chapter 1. (Koifman O.I., Ed.) URSS, 2019. p. 17-62.

819. Krestov A.G., Blokhina S.V., Galyametdinov Yu.G., Ol'khovich M.V., Lokhanov V.V. Russ. J. Phys. Chem. 1993, 67(1), 151-154.

820. Kuvshinov G.V., Maizlish V.E., Kuvshinova S.A., Burmistrov V.A., Koifman O.I. Macroheterocycles 2016, 9(3), 244-249.
https://doi.org/10.6060/mhc160318k

821. Burmistrov V.A., Semeikin A.S., Kuvshinov G.V., Aleksandriiskii V.V., Lubimova T.V., Kuvshinova S.A., Koifman O.I. J. Porphyrins Phthalocyanines 2017, 21, 103-109.
https://doi.org/10.1142/S1088424617500110

822. Sanders J.K.M., Bampos N., Clude-Watson Z., Darling S.L., Hawley J.C., Kim H.-J., Mak C.C., Webb S.J. Axial Coordination Chemistry of Metalloporphyrins. In: The Porphyrin Handbook, Vol. 3, Ch. 15. (Kadish K.M., Smit K.M., Guilard R., Eds.) New York: Academ. Press, 2000. p. 1-47.

823. Grajek H., Witkiewicz Z., Purchała M., Drzewin'ski W. Chromatographia 2016, 79, 1217-1245.
https://doi.org/10.1007/s10337-016-3154-5

824. Burmistrov V.A., Semeikin A.S., Lubimova T.V., Novikov I.V., Litov K.M., Aleksandriiskii V.V., Kuvshinova S.A., Koifman O.I. Nickel Complex of 5,10,15,20-tetrakis[3',5'-di-(2'-methylbutyloxy)phenyl]-porphin Exhibiting the Stationary Phase Property for Gas Chromatography, 2015, Patent RF No 2557655.

825. Allenmark S.G. Chromatographic Enantioseparation: Methods Applications. Chichester: Horwood, 1988. 224 p.

826. Kuvshinov G.V., Koifman O.I. Russ. J. Phys. Chem. A 2018, 92(10), 2025-2031.
https://doi.org/10.1134/S0036024418100163

827. Kuvshinov G.V., Kuvshinova S.A., Burmistrov V.A., Koifman O.I. Sorbent for Gas Chromatography, 2017, Patent RF No 2621 337.

828. Kuvshinov G.V., Kuvshinova S.A., Koifman O.I. J. Anal. Chem. 2017, 72(11), 1172-1177.
https://doi.org/10.1134/S1061934817110065

829. Kuvshinov G.V., Koifman O.I. Russ. J. Gen. Chem. 2019, 89, 1279-1285.
https://doi.org/10.1134/S1070363219060240

830. Executive Orders №1629n dated 29.12.2012 and №915n dated 15.11.2012 of the Ministry of Health of the Russian Federation.

831. Abrahamse H., Hamblin M. Biochem. J. 2016, 473, 347-364.
https://doi.org/10.1042/BJ20150942

832. Kwiatkowski S., Knap B., Przystupski D. et al. Biomedicine & Pharmacotherapy 2018, 106, 1098-1107.
https://doi.org/10.1016/j.biopha.2018.07.049

833. Zhang X.H., Zhang L.J., Sun J.J. et al. Biomedicine & Pharmacotherapy 2016, 81, 265-272.
https://doi.org/10.1016/j.biopha.2016.04.007

834. Mironov A.F. Russ. J. Gen. Chem. 2019, 89, 1952-1983.
https://doi.org/10.1134/S1070363219090354

835. Ethirajan Y., Chen Y., Joshi P., Pandey R.K. Chem. Soc. Rev. 2011, 40, 340-362.
https://doi.org/10.1039/B915149B

836. Senge M.O., Brandt J.C. Photochem. Photobiol. 2011, 87, 1240-1296.
https://doi.org/10.1111/j.1751-1097.2011.00986.x

837. Bonnett R. Chemical Aspects of Photodynamic Therapy. Amsterdam: Gordon and Breach Science Publishers, 2000.
https://doi.org/10.1201/9781482296952

838. Muragaki Y., Akimoto J., Manuyama T. et al. J. Neurosung. 2013, 119, 845-852.
https://doi.org/10.3171/2013.7.JNS13415

839. Kobayashi W., Liu Q., Nakagawa H. et al. Oral. Oncol. 2006, 42, 45-49.
https://doi.org/10.1016/j.oraloncology.2005.05.009

840. Saavedra R., Rocha L.B., Dabrowski J.M. et al. Chem. Med. Chem. 2014, 9, 390-398.
https://doi.org/10.1002/cmdc.201300449

841. Shan W.M., Lim T.H., Pece A., et al. Graefes. Arch. Clin. Exp. Ophthalmol. 2010, 248, 613-626.
https://doi.org/10.1007/s00417-010-1307-z

842. Sessler J.L., Miller R.A. Biochem. Pharmacol. 2000, 59, 733-739.
https://doi.org/10.1016/S0006-2952(99)00314-7

843. Josefsen L.B., Boyle R.W. Metal-Based Drugs 2008, 200, 1-24.
https://doi.org/10.1155/2008/276109

844. Scherz A., Salomon Y. The Story of Tookad, From Bench to Bedside. In: Handbook of Photomedicine. (Hamblin M.R., Huang Y.Y., Eds.) CRC Press, Boca Raton, FL, 2014.
https://doi.org/10.1201/b15582-43

845. Chevalier S., Anidjar M., Scarlata E., et al. J. Urol. 2011, 196, 302-309.
https://doi.org/10.1016/j.juro.2011.03.039

846. Ashur I., Goldschmidt R., Pinkas I., et al. J. Phys. Chem. A 2009, 113, 8027-8037.
https://doi.org/10.1021/jp900580e

847. Scherz A., Salomon Y., Coleman. J. Photodiagn. Photodyn. Ther. 2017, 17, 22-31.
https://doi.org/10.1016/j.pdpdt.2017.01.049

848. Lobel J., MacDonald I.J., Ciesielski M.Y., et al. Laser Surg. Med. 2001, 29, 397-405.
https://doi.org/10.1002/lsm.10001

849. Peng Q., Berg K., Moan J., et al. Photochem. Photobiol. 1997, 65, 235-251.
https://doi.org/10.1111/j.1751-1097.1997.tb08549.x

850. Krammer B., Plaetzer K. Photochem. Photobiol. Sci. 2008, 7, 283-289.
https://doi.org/10.1039/B712847A

851. Furre I.E., Shahzidi S., Luksiene Z., et al. Cancer Res. 2005, 65, 11051-11060.
https://doi.org/10.1158/0008-5472.CAN-05-0510

852. Romanko Y.S., Tsyb A.F., Kaplan M.A., et al. Bull. Exp. Biol. Med. 2004, 138, 584-589.
https://doi.org/10.1007/s10517-005-0133-5

853. Petrov P., Trukacheva T., Kaplan M., 2006, European Patent Application EP 1610821.

854. Biswas R., Moon J.H., Ahn J.C. Photochem. Photobiol. 2014, 90, 1108-1118.
https://doi.org/10.1111/php.12273

855. Pucelic B.L., Arnaut G., Stochel G., et al. ACS Appl. Mater. Interfaces 2016, 8, 22039-22055.
https://doi.org/10.1021/acsami.6b07031

856. Santos L.L., Oliveira J., Monteiro E., et al. Case Rep. Oncol. 2018, 11, 769-776.
https://doi.org/10.1159/000493423

857. Ormond A.B., Freeman H.S. Materials 2013, 6, 817-840.
https://doi.org/10.3390/ma6030817

858. Pereira P.M.R., Korsak B., Sarmento B., et al. Org. Biomol. Chem. 2015, 13, 2518-2529.
https://doi.org/10.1039/C4OB02334J

859. Moret F., Reddi E. J. Porphyrins Phthalocyanines 2017, 21, 1-18.
https://doi.org/10.1142/S1088424616501273

860. Pucelik B., Sułek A., Dąbrowski J.M. Coord. Chem. Rev. 2020, 416 , 213340. https://doi.org/10.1016/j.ccr.2020.213340

861. Mironov A.F., Zhdanova K.A., Bragina N.A. Russ. Chem. Rev. 2018, 87, 859-881.
https://doi.org/10.1070/RCR4811

862. Sandland J., Malatesti N., Boyle R. Photodiagnosis Photodyn. Ther. 2018, 23, 281-294.
https://doi.org/10.1016/j.pdpdt.2018.06.023

863. Boyle R.W., Sandland J. Bioconjugate Chem. 2019, 30, 975-993.
https://doi.org/10.1021/acs.bioconjchem.9b00055

864. Hamblin M.R. Photochem. Photobiol. 2020, 96, 506-516.
https://doi.org/10.1111/php.13190

865. Sato K., Nagaya T., Choyke P.L., et al. Theranostics 2015, 5, 698-709.
https://doi.org/10.7150/thno.11559

866. Parslow A.C., Parakh S., Lee F.T. Biomedicines 2016, 4, 14-31.
https://doi.org/10.3390/biomedicines4030014

867. You H., Yoon H.E., Jeong P.M., et al. Bioorg. Med. Chem. 2015, 23, 1453-1462.
https://doi.org/10.1016/j.bmc.2015.02.014

868. Yang N.J., Hinner M.J. Meth. Mol. Biol. 2015, 126, 29-53.
https://doi.org/10.1007/978-1-4939-2272-7_3

869. Park S.Y., Baik H.J., Oh Y.T., et al. Angew. Chem. Int. Ed. Engl. 2011, 50, 1644-1647.
https://doi.org/10.1002/anie.201006038

870. Singh S., Aggarwal A., Dinesh N.V.S., et al. Chem. Rev. 2015, 115, 10261-10306.
https://doi.org/10.1021/acs.chemrev.5b00244

871. El-Akra N., Noirot A., Faye J.C., et al. Photochem. Photobiol. Sci. 2006, 5, 996-999.
https://doi.org/10.1039/B606117F

872. Stefflova K., Li H., Chen J., et al. Bioconjugate Chem. 2007, 18, 379-388.
https://doi.org/10.1021/bc0602578

873. Gravier J., Schneider R., Frochot C., et al. J. Med. Chem. 2008, 51, 3867-3877.
https://doi.org/10.1021/jm800125a

874. Suvorov N.V., Mironov A.F., Grin M.A. Russ. Chem. Bull. 2017, 1982-2008.
https://doi.org/10.1007/s11172-017-1973-7

875. Barondes S.H., Castronovo V., Cooper D.N.W., et al. Cell 1994, 76, 597-598.
https://doi.org/10.1016/0092-8674(94)90498-7

876. Zheng X., Pandey R.K. Anti-Cancer Agents in Med. Chem. 2008, 8, 241-268.
https://doi.org/10.2174/187152008783961897

877. Aksenova A.A., Sebyakin Yu.L., Mironov A.F. Russ. J. Bioorg. Chem. 2000, 26, 111-124.
https://doi.org/10.1007/BF02759156

878. Aksenova A.A., Sebyakin Yu.L., Mironov A.F. Russ. J. Bioorg. Chem. 2001, 27, 124-129.
https://doi.org/10.1023/A:1011389321240

879. Mironov A.F., Lebedeva V.S. Tetrahedron Lett. 1998, 39, 905-908.
https://doi.org/10.1016/S0040-4039(97)10687-6

880. Lebedeva V.S., Ruziev R.D., Popov A.V., et al. Mendeleev Commun. 2007, 17, 212-213.
https://doi.org/10.1016/j.mencom.2007.06.008

881. Lonin I.S. Ph.D. Thesis in Chemical Science "Synthesis and Examination of Properties of Natural Chlorins and Bacteriochlorins", Moscow, 2009. (in Russ.).

882. Lonin I.S., Lakhina A.A., Grin M.A., et al. Mendeleev Commun. 2012, 22, 157-158.
https://doi.org/10.1016/j.mencom.2012.05.016

883. Grin M.A., Lonin I.S., Makarov A.I., et al. Mendeleev Commun. 2008, 18, 135-137.
https://doi.org/10.1016/j.mencom.2008.05.008

884. Lonin I.S., Makarov A.I., Lakhina A.A., et al. J. Porphyrins Phthalocyanines 2008, 12, 619.

885. Grin M.A., Lonin I.S., Lakhina A.A., Ol'shanskaya E.S., Makarov A.I., Sebyakin Y.L., Guryeva L.Yu., Toukach P.V., Kononikhin A.S., Kuzmin V.A., Mironov A.F. J. Porphyrins Phthalocyanines 2009, 13, 336-345.
https://doi.org/10.1142/S1088424609000425

886. Grin M.A., Plotnikova E.A., Plyutinskaya A.D., et al. Russ. Biother. J. 2012, 11, 14.

887. Petrov P., Trukhacheva T., Isakov G., et al. Acta Bioopt. Inform. Med. 2004, 10, 6-7.

888. Trukhacheva T.V., Shlyahtin S.V., Isakov G.A., et al. Fotolon - A Novel Solution for PDT. Review of the Results of Pharmaceutical, Pharmacological and Clinical Trials. Minsk: RUP "Belmedpreparaty", 2009. p. 64. ISBN 978-5-89552-367-4.

889. Kularatne S.A., Venkatesh C., Santhapuram H.K.R., et al. J. Med. Chem. 2010, 53, 7767-7777.
https://doi.org/10.1021/jm100729b

890. Hillier S.M., Maresca K.P., Lu G., et al. J. Nucl. Med. 2013, 54, 1369-1376.
https://doi.org/10.2967/jnumed.112.116624

891. Stoermer D., Liu Q., Hall M.R., et al. Bioorg. Med. Chem. Lett. 2003, 13, 2097-2100.
https://doi.org/10.1016/S0960-894X(03)00407-4

892. Hargus J.A., Fronczek F.R., Vicente M.G.H., Smith K.M. Photochem. Photobiol. 2007, 83, 1006-1015.
https://doi.org/10.1111/j.1751-1097.2007.00092.x

893. Jinadasa R.G.W., Hu X., Vicente M.G.H., Smith K.M. J. Med. Chem. 2011, 54, 7464-7476.
https://doi.org/10.1021/jm2005139

894. Jinadasa R.G.W., Zhou Z., Vicente M.G.H., Smith K.M. Org. Biomol. Chem. 2016, 14, 1049-1064.
https://doi.org/10.1039/C5OB02241J

895. Bommer J.C., Ogden B.F. Tetrapyrrole Therapeutic Agents, 1987, U.S. Patent 4,693.885.

896. Pandey R.K., Zheng G. Porphyrins as Photosensitizers in Photodynamic Therapy. In: The Porphyrin Handbook. Vol. 6. (Kadish K. M., Smith K. M., Guilard R., Eds.) Boston: Academic Press, 2000. p. 157-230.

897. Suvorov N.V. Ph.D. Thesis in Chemical Science "Modified Natural Chlorins of Targeted Action Against Tumor Cells of Various Genesis", Moscow, 2019.

898. Grin M.A., Suvorov N.V., Machulkin A.E., et al., 2018, Patent RU 2670087 C1.

899. Oliveira B.L., Guo Z., Bernardes G.J.L. Chem. Soc. Rev. 2017, 46, 4895-4950.
https://doi.org/10.1039/C7CS00184C

900. Suvorov N.V., Cheskov D.A., Mironov A.F., et al. Mendeleev Commun. 2019, 29, 206-207.
https://doi.org/10.1016/j.mencom.2019.03.031

901. Suvorov N.V., Machulkin A.E., Ivanova A.V., et al. J. Porphyrins Phthalocyanines 2018, 22, 1030-1038.
https://doi.org/10.1142/S1088424618501006

902. Selbo P.K., Bostad M., Olsen C.E., et al. Photochem. Photobiol. Sci. 2015, 14, 1433-1450.
https://doi.org/10.1039/C5PP00027K

903. Sultan A.A., Jerjes W., Berg K., et al. Lancet Oncol. 2016, 17, 1217-1229.
https://doi.org/10.1016/S1470-2045(16)30224-8

904. Kochneva E.V., Filonenko E.V., Vakulovskaya E.G., et al. Photodiagnosis Photodyn. Ther. 2010, 7, 258-267.
https://doi.org/10.1016/j.pdpdt.2010.07.006

905. Shiryaev A.A., Musaev G.K., Levkin V.V., et al. Photodiagnosis Photodyn. Ther. 2019, 26, 218-223.
https://doi.org/10.1016/j.pdpdt.2019.04.006

906. Baker M. Nature 2010, 463, 977-980.
https://doi.org/10.1038/463977a

907. Thorp-Greewood F.L., Coogan M.P. Dalton Trans. 2011, 40, 6129-6143.
https://doi.org/10.1039/c0dt01398f

908. Mewis R.E., Archibald S.J. Coord. Chem. Rev. 2010, 254, 1682-1712.
https://doi.org/10.1016/j.ccr.2010.02.025

909. Rashid H.U., Khan K., Yaseen M., et al. Rev. Roum. Chim. 2014, 59, 27-33.

910. Grin M.A., Brusov S.S., Shchepelina E.Y., et al. Mendeleev Commun. 2017, 27, 338-340.
https://doi.org/10.1016/j.mencom.2017.07.005

911. Mironov A.F. Transition Metal Complexes of Porphyrins and Porphyrinoids. In: Handbook of Porphyrin Science. Vol 18. Applications and Materials. (Kadish K.M., Smith K.M., Guillard R., Eds). World Scientific, 2012. p. 304-413.
https://doi.org/10.1142/9789814335508_0012

912. Rumyantseva V.D., Shchelkunova A.E., Gorshkova A.S., Alekseev Yu.V., Shumilova N.M., Shilov I.P., Ivanov A.V., Mironov A.F. Fine Chem. Technol. 2017, 12, 72-80.
https://doi.org/10.32362/2410-6593-2017-12-2-72-80

913. Smirnov A.S., Grin M.A., Mironov A.F. Fine Chem. Technol. 2019, 14, 95-103.
https://doi.org/10.32362/2410-6593-2019-14-6-95-103

914. Brusov S.S. Ph.D. Thesis in Chemical Science "Natural Chlorins with Photoinduced Antibacterial, Antitumor Activity and Diagnostic Potential", Moscow, 2018.

915. Zenkevich E., Sagun E., Knyukshto V., Shulga A., Mironov A., Efremova O., Bonnett R., Songca S.P., Kassem M.J. Photochem. Photobiol. B: Biol. 1996, 33, 171-180.
https://doi.org/10.1016/1011-1344(95)07241-1

916. Parkhats M.V., Galievsky V.A., Stashevsky A.S., Trukhacheva T.V., Dzhagarov B.M. Opt. Spectrosc. 2009, 107(6), 974-980.
https://doi.org/10.1134/S0030400X09120200

917. Henderson B.W., Sumlin A.B., Owcharczak B.L., Dougherty T.J. Photochem.Photobiol. B 1991, 10, 303-313.
https://doi.org/10.1016/1011-1344(91)80016-B

918. Koudinova N.V., Pinthus J.H., Brandis A., Brenner O., Bendel P., Ramon J., Eshhar Z., Scherz A., Salomon Y. Int. J. Cancer 2003, 104, 782-789.
https://doi.org/10.1002/ijc.11002

919. Brandis A., Mazor O., Neumark E., Rozenbach V.-Belkin, Salomon Y., Scherz A. Photochem. Photobiol. 2005, 81, 983-993.
https://doi.org/10.1562/2004-12-01-RA-389R1.1

920. Grin M.A., Mironov A.F., Shtil A.A. Anti-Cancer Agents in Med. Chem. 2008, 8, 683-697.
https://doi.org/10.2174/187152008785133128

921. Grin M.A., Mironov A.F. In: Chemical Processes with Participation of Biological and Related Compounds (Lomova T.N., Zaikov G. T., Ed.) Boston, Brill: Leiden, 2008. p. 5-43.

922. Eisner U. J. Chem. Soc. 1957, 3461-3469.
https://doi.org/10.1039/jr9570003461

923. Scheer H. Chlorophylls. Boston, London: CRC Press, Boca Raton Ann Arbor, 1991. p. 115-143.

924. Mironov A.F., Efremov A.V., 1996, Patent RF No 2144085.

925. Tsygankov A.A., Laurinavichene T.V., Gogotov I.N. Biotechnol. Tech. 1994, 8, 575-578.
https://doi.org/10.1007/BF00152149

926. Tsygankov A.A., Laurinavichene T.V., Bukatin V.E., Gogotov I.N., Hall D.O. Biochem. Microbiol. 1997, 33, 485-490.

927. Prinsep M.R., Caplan F.R., Moore R.E., Patterson G.M.L., Smith C.D. J. Am. Chem. Soc. 1992, 114, 385-387.
https://doi.org/10.1021/ja00027a072

928. Prinsep M.R., Patterson G.M.L., Larsen L.K., Smith C. D. Tetrahedron 1995, 51, 10523-10530.
https://doi.org/10.1016/0040-4020(95)00615-F

929. Prinsep M.R., Patterson G.M.L., Larsen L.K., Smith C. D. J. Nat. Prod. 1998, 61, 1133-1136.
https://doi.org/10.1021/np970566+

930. Prinsep M.R., Appleton T.G., Hanson G.R., Lane I., Smith C.D., Puddick J., Fairlie, D.P. Inorg. Chem. 2017, 56, 5577-5585.
https://doi.org/10.1021/acs.inorgchem.6b03000

931. Minehan T.G., Kishi Y. Angew. Chem. Int. Ed. 1999, 38, 923−925.
https://doi.org/10.1002/(SICI)1521-3773(19990401)38:7<923::AID-ANIE923>3.0.CO;2-7

932. Minehan T.G., Cook-Blumberg L., Kishi Y., Prinsep M.R., Moore R.E. Angew. Chem. Int. Ed. 1999, 38, 926−928.
https://doi.org/10.1002/(SICI)1521-3773(19990401)38:7<926::AID-ANIE926>3.0.CO;2-W

933. Hoebeke M., Schuitmaker H.J., Jannink L.E., et al. Photochem. Photobiol. 1997, 66, 502-508.
https://doi.org/10.1111/j.1751-1097.1997.tb03180.x

934. Fiedor L., Rosenbach-Belkin V., Sai M., Scherz A. Plan. Physiol. Biochem. 1996, 34, 393-398.

935. Scherz A., Salomon Y., Brandis A., Scheer H., 2000, PCT Patent WO00/33833.

936. Ashur I., Goldschmidt R., Pinkas I., Salomon Y., Szewczyk G., Sarna T., Scherz A. J. Phys. Chem. A 2009, 113, 8027-8037.
https://doi.org/10.1021/jp900580e

936. Azzouzi A. R., Barret E., Bennet J., Moore C., Taneja S., Muir G., Villers A., Coleman J., Allen C., Scherz A., Emberton M. World J. Urology 2015, 33 , 945-953.
https://doi.org/10.1007/s00345-015-1505-8

937. Vakrat-Haglili Y., Weiner L., Brumfeld V., Brandis A., Salomon Y., McIlroy B., Wilson B.C., Pawlak A., Rozanowska M., Sarna T., Scherz A. J. Am. Chem. Soc. 2005, 127, 6487-6497.
https://doi.org/10.1021/ja046210j

938. Sasaki S., Tamiaki H. J. Org. Chem. 2006, 71, 2648-2654.
https://doi.org/10.1021/jo0523969

939. Mironov A.F., Kozyrev A.N., Brandis A.S. Proc. SPIE 1992, 1922, 204-208.

940. Fischer H., Lambrecht R., Mittenzwei H.Z. Physiol. Chem. 1939, 1, 253-259.

941. Hartwich G., Fiedor L., Simonin I., Cmiel E., Schafer W., Noy D., Scherz A., Scheer H. J. Am. Chem. Soc. 1998, 120, 3675-3683.
https://doi.org/10.1021/ja970874u

942. Kozyrev A.N., Chen Y., Goswami L.N., Tabaczynski W.A., Pandey R.K. J. Org.Chem. 2006, 71, 1949-1960.
https://doi.org/10.1021/jo052334i

943. Waielewski M.R., Svec W.A. J. Org. Chem. 1980, 45, 1969-1974.
https://doi.org/10.1021/jo01298a043

944. Chen Y., Potter W.R., Missert J.R., Morgan J., Pandey R.K. Bioconjugate Chem. 2007, 18, 1460-1473.
https://doi.org/10.1021/bc070092i

945. Saga Y., Ishitani A., Takahashi N., Kawamura K. Bioorg. Med. Chem. Lett. 2015, 25, 639-641.
https://doi.org/10.1016/j.bmcl.2014.12.002

946. Kozyrev A., Ethirajan, M., Chen P., Ohkubo K., Robinson B.C., Barkigia K.M., Pandey R.K. J. Org. Chem. 2012, 77, 10260-10271.
https://doi.org/10.1021/jo301895p

947. Kozyrev A.N., Zheng G., Zhu C.F. Tetrahedron Lett. 1996, 37, 6431-6434.
https://doi.org/10.1016/0040-4039(96)01346-9

948. Pandey R.K., Sumlin A.B., Constantine S., Aoudia M., Potter W.R., Bellnier D.A., Henderson B.W., Rodgers M.A., Smith K.M., Dougherty T.J. Photochem. Photobiol. 1996, 64, 194-204.
https://doi.org/10.1111/j.1751-1097.1996.tb02442.x

949. Grin M.A., Lonin I.S., Likhosherstov L.M., Novikova O.S., Plyutinskaya A.D., Plotnikova E.A., Kachala V.V., Yakubovskaya R.I., Mironov A.F. J. Porphyrins Phthalocyanines 2012, 16, 1094-1109.
https://doi.org/10.1142/S1088424612500848

950. Gorshkova A.S., Rumyantseva V.D., Mironov A.F. Fine Chem. Technol. 2018, 13(2), 5-20.
https://doi.org/10.32362/2410-6593-2018-13-2-5-20

951. Patel N., Pera P., Joshi P., Dukh M., Tabaczynski W.A., Siters K.E., Pandey R.K. J. Med. Chem. 2016, 59, 9774-9787.
https://doi.org/10.1021/acs.jmedchem.6b00890

952. Plotnikova E.A., Stramova V.O., Morozova N.B., Plyutinskaya A.D., Ostroverkhov P.V., Grin M.A., Mironov A.F., Yakubovskaya R.I., Kaprin A.D. Biomed. Photon. 2019, 8, 18-23.
https://doi.org/10.24931/2413-9432-2019-8-1-18-23

953. Mironov A.F., Grin M.A., Tsiprovskiy A.G., Kachala V.V., Karmakova T.A., Plyutinskaya A.D., Yakubovskaya R.I. J. Porphyrins Phthalocyanines 2003, 7, 725-730.
https://doi.org/10.1142/S1088424603000902

954. Mironov A.F., Grin M.A., Tsiprovskiy A.G., Dzardanov D.V., Golovin K.V., Feofanov A.V., 2004, Patent RF No 2223274.

955. Brusov S.S., Grin M.A., Meerovich G.A., Mironov A.F., Romanova Yu. M., Tiganova I.G., 2017, Patent RF No 2610566.

956. Pantyushenko I.V., Rudakovskaya P.G., Starovoitova A.V., Mikhailovskaya A.A., Abakumov M.A., Kaplan M.A., Tsigankov A.A., Majouga A.G., Grin M.A., Mironov A.F. Biochemistry 2015, 80, 752-762.
https://doi.org/10.1134/S0006297915060103

957. Mironov A.F., Grin M.A. J. Porphyrins Phthalocyanines 2008, 12, 1163-1172.
https://doi.org/10.1142/S1088424608000534

958. Grin M.A., Brittal D.I., Tsiprovskiy A.G., Bregadze V.I., Mironov A.F. Macroheterocycles 2010, 3, 222-227.
https://doi.org/10.6060/mhc2010.4.222

959. Meerovich I.G., Tsyprovskiy A.G., Meerovich G.A., Barkanova S.V., Borisova L. M., Oborotova N. A., Baryshnikov A.Yu., Mironov A.F. Proc. SPIE 2007, 6427, 64270W1-W9.

960. Chissov V.I., Yakubovskaya R.I., Mironov A.F., Grin M.A., Plotnikova E.A., Morozova N.B., Tsigankov A.A., 2012, Patent RF No 2521327.

961. Grin M.A., Filonenko E.V., Mironov A.F., Suvorov N.B., Pankratov A.A., Grigor'evukh N.I., 2020, Patent RF No 2720806.

962. Aravindu K., Krayer M., Kim H.-J., Lindsey J.S. New J. Chem. 2011, 35, 1376-1384.
https://doi.org/10.1039/c1nj20027e

963. Senge M.O., Wiehe A., Ryppa C. Adv. Photosynth. Respir. 2006, 25, 27-37.

964. Lange C., Bednarski P.J. Curr. Pharmac. Design 2016, 22, 6956-6974.
https://doi.org/10.2174/1381612822666161124155344

965. Pucelik B., Arnaut L.G., Stochel G., Dabrowski J.M. ACS Appl. Mater. Interfaces 2016, 8, 22039-22055.
https://doi.org/10.1021/acsami.6b07031

965. Karwicka M., Pucelik B., Gonet M., Elas M., Dąbrowski J.M.. Scientific Reports 2019, 9, 12655.
https://doi.org/10.1038/s41598-019-49064-6

966. Bruhn T., Brückner C. J. Org. Chem. 2015, 80, 4861-4868. 
https://doi.org/10.1021/acs.joc.5b00137

967. Samankumara L.P., Zeller M., Krause J.A., Brückner C. Org. Biomol. Chem. 2010, 8, 1951-1965.
https://doi.org/10.1039/b924539a

968. Ke X.S., Yang B.Y., Cheng X., Chan S.L.F., Zhang J.L. Chem. Eur. J. 2014, 20, 4324-4333.
https://doi.org/10.1002/chem.201303972

969. MacGowan S.A., Senge M.O. Chem. Commun. 2011, 47, 11621-11623.
https://doi.org/10.1039/c1cc14686f

970. MacGowan S.A., Senge M.O. Biochim. Biophys. Acta 2016, 1857, 427-442.
https://doi.org/10.1016/j.bbabio.2016.02.001

971. Guberman-Pfeffer M.J., Greco J.A., Samankumara L.P., Zeller M., Birge R.R., Gascon J.A., Brückner C. J. Am. Chem. Soc. 2017, 139, 548-560.
https://doi.org/10.1021/jacs.6b12419

972. Herges R., Peters M.K., 2020, Patent EP 3653226.

973. Peters M.K., Herges R. Beilstein J. Org. Chem.2017, 13, 2659-2662.
https://doi.org/10.3762/bjoc.13.263

974. Peters M.K., Röhricht F., Näther C., Herges R. Org. Lett. 2018, 20(24), 7879-7883.
https://doi.org/10.1021/acs.orglett.8b03433

975. Li G., Graham A., Chen Y., Dobhal M.P., Morgan J., Zheng G., Kozyrev A., Oseroff A., Dougherty T.J., Pandey R.K. J. Med. Chem. 2003, 46, 5349-5359.
https://doi.org/10.1021/jm030341y

976. Kim H.-J., Lindsey J.S. J. Org. Chem. 2005, 70, 5475-5486.
https://doi.org/10.1021/jo050467y

977. Krayer M., Ptaszek M., Kim H.-J., Meneely K.R., Fan D., Secor K., Lindsey J.S. J. Org. Chem. 2010, 75, 1016-1039.
https://doi.org/10.1021/jo9025572

978. Reddy K.R., Lubian E., Pavan M.P., Kim H.-J., Yang E., Holten D., Lindsey J.S. New J. Chem. 2013, 37, 1157-1173.
https://doi.org/10.1039/c3nj41161c

979. Zhang S., Kim H.-J, Tang Q., Yang E., Bocian D.F., Holten D., Lindsey J.S. New J. Chem. 2016, 40, 5942-5956.
https://doi.org/10.1039/C6NJ00517A

980. Liu Y., Lindsey J.S. J. Org. Chem. 2016, 81, 11882−11897.
https://doi.org/10.1021/acs.joc.6b02334

981. Esemoto N.N., Yu Z., Wiratan L., Satraitis A., Ptaszek M. Org. Lett. 2016, 18, 4590-4593.
https://doi.org/10.1021/acs.orglett.6b02237

982. Bennion M.C., Burch M.A., Dennis D.G., Lech M.E., Neuhaus K., Fendler N.L., Parris M.R., Cuadra J.E., Dixon C.F., Mukosera G.T., Blauch D.N., Hartmann L., Snyder N.L., Ruppel, J.V. Eur. J. Org. Chem. 2019, 2019, 6496-6503.
https://doi.org/10.1002/ejoc.201901128

983. Ogata F., Nagaya T., Maruoka Y., Akhigbe J., Meares A., Lucero M.Y., Satraitis A., Fujimura D., Okada R., Inagaki F., Choyke P.L., Ptaszek M., Kobayashi H. Bioconjugate Chem. 2019, 30, 169-183.
https://doi.org/10.1021/acs.bioconjchem.8b00820

984. Ballatore M.B., Milanesio M.E., Fujita H., Lindsey J.S., Durantini E.N. J. Biophotonics 2020, 13, e201960061.
https://doi.org/10.1002/jbio.201960061

985. Jiang J., Taniguchi M., Lindsey J.S. New J. Chem. 2015, 39, 4534-4550.
https://doi.org/10.1039/C5NJ00209E

986. Vairaprakash P., Yang E., Sahin T., Taniguchi M., Krayer M., Diers J.R., Wang A., Niedzwiedzki D.M., Kirmaier C., Lindsey J.S., Bocian D.F., Holten D. J. Phys. Chem. B 2015, 119, 4382-4395.
https://doi.org/10.1021/jp512818g

987. Krayer M., Yang E., Diers J.R., Bocian D.F., Holten D., Lindsey J.S. New J. Chem. 2011, 35, 587-601.
https://doi.org/10.1039/c0nj00771d

988. Fujita H., Jing H., Krayer M., Allu S., Veeraraghavaiah G., Wu Z., Jiang J., Diers J.R., Magdaong N.C.M., Mandal A.K., Roy A., Niedzwiedzki D.M., Kirmaier C., Bocian D.F., Holten D., Lindsey J.S. New J. Chem. 2019, 43, 7209-7232.
https://doi.org/10.1039/C9NJ01113G

989. Zhang S., Lindsey J.S. J. Org. Chem. 2020, 82, 2489-2504.
https://doi.org/10.1021/acs.joc.6b02878

990. Woodward R.B., Ayer W.A. Beaton J.M., Bickelhaupt F., Bonnett R., Buchschacher P., Closs G.L., Dutler H., Hannah J., Hauck F.P., Itô S., Langemann A., Le Goff E., Leimgruber W., Lwowski W., Sauer J., Valenta Z., Volz H. J. Am. Chem. Soc. 1960, 82, 3800−3802.
https://doi.org/10.1021/ja01499a093

991. Woodward R.B. Pure Appl. Chem. 1961, 2, 383−404.
https://doi.org/10.1351/pac196102030383

992. Liu M., Chen C.-Y., Hood D., Taniguchi M., Diers J.R., Bocian D.F., Holten D., Lindsey J.S. New J. Chem. 2017, 41, 3732-3744.
https://doi.org/10.1039/C6NJ04135C

993. van Straten D., Mashayekhi V., de Bruijn H.S., Oliveira S., Robinson D. J. Cancers (Basel) 2017, 9, 1-54.
https://doi.org/10.3390/cancers9020019

994. Agostinis P., Berg K., Cengel K.A., Foster T.H., Girotti A.W., Gollnick S.O., Hahn S.M., Hamblin M.R., Juzeniene A., Kessel D., Korbelik M., Moan J., Mroz P., Nowis D., Piette J., Wilson B.C., Golab J. Cancer J. Clin. 2017, 61, 250-281.
https://doi.org/10.3322/caac.20114

995. Babilas P., Schreml S., Landthaler M., Szeimies R.-M. Photodermatol. Photoimmunol. Photomed. 2010, 26, 118-132.
https://doi.org/10.1111/j.1600-0781.2010.00507.x

996. Kharkwal G.B., Sharma S.K., Huang Y.Y., Dai T., Hamblin M.R. Lasers Surg. Med. 2011, 43, 755-767.
https://doi.org/10.1002/lsm.21080

997. Allison R.R., Sibata C.H. Photodiagnosis Photodyn. Ther. 2010, 7, 61-75.
https://doi.org/10.1016/j.pdpdt.2010.02.001

998. Knap B., Przystupski D., Saczko J., Ewa K., Knap-czop K., Kotli J., Michel O., Kotowski K. Kulbacka J. 2018, 106, 1098-1107.
https://doi.org/10.1016/j.biopha.2018.07.049

999. Zhang J., Jiang C., Paulo J., Longo F., Bentes R., Zhang H., Alexandre L. Acta Pharm. Sin. B 2018, 8, 137-146.
https://doi.org/10.1016/j.apsb.2017.09.003

1000. Cai L., Gu Z., Zhong J., Wen D., Chen G., He L., Wu J., Gu Z. Drug Discov. Today 2018, 23, 1126-1138.
https://doi.org/10.1016/j.drudis.2018.02.009

1001. Yoo J., Park C., Yi G., Lee D., Koo H. Cancers (Basel) 2019, 11, 640.
https://doi.org/10.3390/cancers11050640

1002. Chen F., Huang G., Huang H. Future Med. Chem. 2020, 12, 161-171.
https://doi.org/10.4155/fmc-2019-0114

1003. Kang B., Opatz T., Landfester K., Wurm F.R. Chem. Soc. Rev. 2015, 44, 8301-8325.
https://doi.org/10.1039/C5CS00092K

1004. Zhao K., Li D., Shi C., Ma X., Rong G., Kang H., Wang X., Sun B. Curr. Drug Deliv. 2016, 13, 494-499.
https://doi.org/10.2174/156720181304160521004609

1005. Lee E., Lee J., Lee I.-H., Yu M., Kim H., Chae S.Y., Jon S. J. Med. Chem. 2008, 51, 6442-6449.
https://doi.org/10.1021/jm800767c

1006. Khatun Z., Nurunnabi M., Reeck G.R., Cho K.J., Lee Y. J. Control. Release 2013, 170, 74-82.
https://doi.org/10.1016/j.jconrel.2013.04.024

1007. Hyung Park J., Kwon S., Lee M., Chung H., Kim J.-H., Kim Y.-S., Park R.-W., Kim I.-S., Bong Seo S., Kwon I. C., Young Jeong S. Biomaterials 2006, 27, 119-126.
https://doi.org/10.1016/j.biomaterials.2005.05.028

1008. Park J.H., Cho Y.W., Son Y.J., Kim K., Chung H., Jeong S.Y., Choi K., Park C.R., Park R.-W., Kim I.-S., Kwon I.C. Colloid Polym. Sci. 2006, 284, 763-770.
https://doi.org/10.1007/s00396-005-1438-7

1009. Voszka I., Galántai R., Maillard P., Csík G. J. Photochem. Photobiol. B Biol. 1999, 52, 92-98.
https://doi.org/10.1016/S1011-1344(99)00107-4

1010. Kaldapa C., Blais J.C., Carré V., Granet R., Sol V., Guilloton M., Spiro M., Krausz P. Tetrahedron Lett. 2000, 41, 331-335.
https://doi.org/10.1016/S0040-4039(99)02085-7

1011. Davoust E., Granet R., Krausz P., Carré V., Guilloton M. Tetrahedron Lett. 1999, 40, 2513-2516.
https://doi.org/10.1016/S0040-4039(99)00259-2

1012. Oulmi D., Maillard P., Guerquin-Kern J.L., Huel C., Momenteau M. J. Org. Chem. 1995, 60, 1554-1564.
https://doi.org/10.1021/jo00111a013

1013. Sol V., Blais J.C., Carré V., Granet R., Guilloton M., Spiro M., Krausz P. J. Org. Chem. 1999, 64, 4431-4444.
https://doi.org/10.1021/jo982499+

1014. Kuzmina N.S., Otvagin V.F., Krylova L.V., Nyuchev A.V., Romanenko Y.V., Koifman O.I., Balalaeva I.V., Fedorov A.Y. Mendeleev Commun. 2020, 30, 159-161.
https://doi.org/10.1016/j.mencom.2020.03.009

1015. Pandey S.K., Zheng X., Morgan J., Missert J.R., Liu T.H., Shibata M., Bellnier D.A., Oseroff A.R., Henderson B.W., Dougherty T.J., Pandey R.K. Mol. Pharm. 2007, 4, 448-464.
https://doi.org/10.1021/mp060135x

1016. Laville I., Figueiredo T., Loock B., Pigaglio S., Maillard P., Grierson D.S., Carrez D., Croisy A., Blais J. Bioorg. Med. Chem. 2003, 11, 1643-1652.
https://doi.org/10.1016/S0968-0896(03)00050-6

1017. Laville I., Pigaglio S., Blais J.C., Loock B., Maillard P., Grierson D.S., Blais J. Bioorg. Med. Chem. 2004, 12, 3673-3682.
https://doi.org/10.1016/j.bmc.2004.04.022

1018. Bautista-Sanchez A., Kasselouri A., Desroches M.C., Blais J., Maillard P., de Oliveira D.M., Tedesco A.C., Prognon P., Delaire J. J. Photochem. Photobiol. B Biol. 2005, 81, 154-162.
https://doi.org/10.1016/j.jphotobiol.2005.05.013

1019. Silva S., Pereira P.M.R., Silva P., Almeida Paz F.A., Faustino M.A.F., Cavaleiro J.A.S., Tomé J.P.C. Chem. Commun. 2012, 48, 3608-3610.
https://doi.org/10.1039/c2cc17561d

1020. Pereira P.M.R., Silva S., Bispo M., Zuzarte M., Gomes C., Girão H., Cavaleiro J.A.S., Ribeiro C.A.F., Tomé J.P.C., Fernandes R. Bioconjugate Chem. 2016, 27, 2762-2769.
https://doi.org/10.1021/acs.bioconjchem.6b00519

1021. Liu F., Rabinovich G.A. Nat. Rev. Cancer 2005, 5, 29-41.
https://doi.org/10.1038/nrc1527

1022. Thijssen V.L., Heusschen R., Caers J., Griffioen A.W. Biochim. Biophys. Acta 2015, 1855, 235-247.
https://doi.org/10.1016/j.bbcan.2015.03.003

1023. Yang F., Zhang Y., Liang H. Int. J. Mol. Sci. 2014, 15, 3580-3595.
https://doi.org/10.3390/ijms15033580

1024. D'Auria S., Petrova L., John C., Russev G., Varriale A., Bogoeva V. Mol. Biosyst. 2009, 5, 1331-1336.
https://doi.org/10.1039/b905921k

1025. Tannock I.F., Rotin D. Cancer Res. 1989, 49, 4373-4384.

1026. Huber V., Camisaschi C., Berzi A., Ferro S., Lugini L., Triulzi T., Tuccitto A., Tagliabue E., Castelli C., Rivoltini L. Semin. Cancer Biol. 2017, 43, 74-89.
https://doi.org/10.1016/j.semcancer.2017.03.001

1027. Lee E.S., Kim D., Youn Y.S., Oh K.T., Bae Y.H. Angew. Chem. Int. Ed. 2008, 47, 2418-2421.
https://doi.org/10.1002/anie.200704121

1028. Biscaglia F., Gobbo M. Pept. Sci. 2018, 110, e24038.
https://doi.org/10.1002/pep2.24038

1029. Almeida-Marrero V., Van De Winckel E., Anaya-Plaza E., Torres T., De La Escosura A. Chem. Soc. Rev. 2018, 47, 7369-7400.
https://doi.org/10.1039/C7CS00554G

1030. Lin Y., Zhou T., Bai R., Xie Y. J. Enzyme Inhib. Med. Chem. 2020, 35, 1080-1099.
https://doi.org/10.1080/14756366.2020.1755669

1031. Ranyuk E., Cauchon N., Klarskov K., Guérin B., Van Lier J.E. J. Med. Chem. 2013, 56, 1520-1534.
https://doi.org/10.1021/jm301311c

1032. Bullous A.J., Alonso C.M.A., Boyle R.W. Photochem. Photobiol. Sci. 2011, 10, 721-750.
https://doi.org/10.1039/c0pp00266f

1033. Zhu L., Liu J., Zhou G., Ng H.M., Ang I.L., Ma G., Liu Y., Yang S., Zhang F., Miao K., Poon T.C.W., Zhang X., Yuan Z., Deng C.X., Zhao Q. Chem. Commun. 2019, 55, 14255-14258.
https://doi.org/10.1039/C9CC06839B

1034. Picarda E., Ohaegbulam K.C., Zang X. Clin. Cancer Res. 2016, 22, 3425-3431.
https://doi.org/10.1158/1078-0432.CCR-15-2428

1035. Teunissen A.J.P., Pérez-Medina C., Meijerink A., Mulder W.J.M. Chem. Soc. Rev. 2018, 47, 7027-7044.
https://doi.org/10.1039/C8CS00278A

1036. Zheng G., Chen J., Stefflova K., Jarvi M., Li H., Wilson B.C. Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 8989-8994.
https://doi.org/10.1073/pnas.0611142104

1037. Overall C.M., Kleifeld O. Nat. Rev. Cancer 2006, 6, 227-239.
https://doi.org/10.1038/nrc1821

1038. Bolze F., Jenni S., Sour A., Heitz V. Chem. Commun. 2017, 53, 12857-12877.
https://doi.org/10.1039/C7CC06133A

1039. Kobayashi H., Ogawa M., Alford R., Choyke P. L., Urano Y. Chem. Rev. 2010, 110, 2620-2640.
https://doi.org/10.1021/cr900263j

1040. Collins H.A., Khurana M., Moriyama E.H., Mariampillai A., Dahlstedt E., Balaz M., Kuimova M.K., Drobizhev M., Yang V.X.D., Phillips D., Rebane A., Wilson B.C., Anderson H.L. Nat. Photonics 2008, 2, 420-424.
https://doi.org/10.1038/nphoton.2008.100

1041. Ke H., Wang H., Wong W.K., Mak N.K., Kwong D.W.J., Wong K.L., Tam H.L. Chem. Commun. 2010, 46, 6678-6680.
https://doi.org/10.1039/c0cc01848a

1042. Poon C.T., Chan P.S., Man C., Jiang F.L., Wong R.N.S., Mak N.K., Kwong D.W.J., Tsao S.W., Wong W.K. J. Inorg. Biochem. 2010, 104, 62-70.
https://doi.org/10.1016/j.jinorgbio.2009.10.004

1043. Ke M., Chen S., Peng X., Zheng Q., Zheng B., Yeh C., Huang J. Eur. J. Med. Chem. 2017, 127, 200-209.
https://doi.org/10.1016/j.ejmech.2016.12.056

1044. Abu-Surrah A., Kettunen M. Curr. Med. Chem. 2006, 13, 1337-1357.
https://doi.org/10.2174/092986706776872970

1045. Brunner H., Schellerer K.M. Monatsh. Chem. 2002, 133, 679-705.
https://doi.org/10.1007/s007060200041

1046. Lottner C., Bart K. C., Bernhardt G., Brunner H. J. Med. Chem. 2002, 45, 2064-2078.
https://doi.org/10.1021/jm0110688

1047. Lottner C., Knuechel R., Bernhardt G., Brunner H. Cancer Lett. 2004, 203, 171-180.
https://doi.org/10.1016/j.canlet.2003.09.001

1048. Bio M., Rajaputra P., Nkepang G., Awuah S.G., Hossion A.M.L., You Y. J. Med. Chem. 2013, 56, 3936-3942.
https://doi.org/10.1021/jm400139w

1049. Rajaputra P., Bio M., Nkepang G., Thapa P., Woo S., You Y. Bioorg. Med. Chem. 2016, 24, 1540-1549.
https://doi.org/10.1016/j.bmc.2016.02.025

1050. Bio M., Rajaputra P., Nkepang G., You Y. J. Med. Chem. 2014, 57, 3401-3409.
https://doi.org/10.1021/jm5000722

1051. Thapa P., Li M., Bio M., Rajaputra P., Nkepang G., Sun Y., Woo S., You Y. J. Med. Chem. 2016, 59, 3204-3214.
https://doi.org/10.1021/acs.jmedchem.5b01971

1052. Zhou X.Q., Meng L.B., Huang Q., Li J., Zheng K., Zhang F.L., Liu J.Y., Xue J.P. ChemMedChem 2015, 10, 304-311.
https://doi.org/10.1002/cmdc.201402401

1053. Tomanová P., Rimpelová S., Jurášek M., Buděšínský M., Vejvodová L., Ruml T., Kmoníčková E., Drašar P. B. Steroids 2015, 97, 8-12.
https://doi.org/10.1016/j.steroids.2014.08.024

1054. Tuncel S., Trivella A., Atilla D., Bennis K., Savoie H., Albrieux F., Delort L., Billard H., Dubois V., Ahsen V., Caldefie-Chézet F., Richard C., Boyle R.W., Ducki S., Dumoulin F. Mol. Pharm. 2013, 10, 3706-3716.
https://doi.org/10.1021/mp400207v

1055. Zhao X., Ma H., Chen J., Zhang F., Jia X., Xue J. Eur. J. Med. Chem. 2019, 182, 111625.
https://doi.org/10.1016/j.ejmech.2019.111625

1056. Otvagin V.F., Kuzmina N.S., Krylova L.V., Volovetsky A.B., Nyuchev A.V., Gavryushin A.E., Meshkov I.N., Gorbunova Y.G., Romanenko Y.V., Koifman O.I., Balalaeva I.V., Fedorov A.Y. J. Med. Chem. 2019, 62, 11182-11193.
https://doi.org/10.1021/acs.jmedchem.9b01294

1057. Maisch T., Eichner A., Späth A., Gollmer A., König B., Regensburger J., Bäumler W. PLOS ONE 2014, 1-18.
https://doi.org/10.1371/journal.pone.0111792

1058. Wainwright M., Maisch T., Nonell S., Plaetzer K., Almeida A., Tegos G.P., Hamblin M.R. Lancet Infect Dis. 2017, 17(2), e49-e55.
https://doi.org/10.1016/S1473-3099(16)30268-7

1059. Yao L., Rong Q., Zaat S.A.J., Breukink E., Heger M. J. Clin. Transl. Res. 2015, 1(3), 140-167.
https://doi.org/10.18053/jctres.201503.002

1060. Hamblin M.R. Curr. Opin. Microbiol. 2016, 33, 67-73.
https://doi.org/10.1016/j.mib.2016.06.008

1061. Huang L., Dai T., Hamblin M.R. Antimicrobial Photodynamic Inactivation and Photodynamic Therapy for Infections. In: Photodynamic Therapy. Methods and Protocols (Gomer C.J., Ed.) New York: Springer, 2010. p. 155-174.
https://doi.org/10.1007/978-1-60761-697-9_12

1062. Kustov A.V., Smirnova N.L., Berezin M.B. Thermochim. Acta 2011, 521, 224-226.
https://doi.org/10.1016/j.tca.2011.02.020

1063. Kustov A.V., Smirnova N.L., Berezin D.B., Berezin M.B. J. Chem. Thermodyn. 2015, 89, 123-126.
https://doi.org/10.1016/j.jct.2015.05.016

1064. Berezin D.B., Karimov D.R., Venediktov E.A., Kustov A.V., Makarov V.V., Romanenko Y.V. Macroheterocycles 2015, 8(4), 384-388.
https://doi.org/10.6060/mhc151088b

1065. Kustov A.V., Smirnova N.L., Berezin D.B., Berezin M.B. J. Chem. Thermodyn. 2015, 83, 104-109.
https://doi.org/10.1016/j.jct.2014.12.013

1066. Kustov A.V., Garas'ko E.V., Belykh D.V., Khudyaeva I.S., Startseva O.M., Makarov V.V., Strel'nikov A.I., Berezin D.B. Usp. Sovrem. Estestvozn. 2016, 12, 263-268. (in Russ.).
https://doi.org/10.17513/use.36297

1067. Kustov A.V., Belykh D.V., Smirnova N.L., Khudyaeva I.S., Berezin D.B. J. Chem. Thermodyn. 2017, 115, 302-306.
https://doi.org/10.1016/j.jct.2017.07.031

1068. Kustov A.V., Antonova O.A., Smirnova N.L., Khudyaeva I.S., Belykh D.V., Berezin D.B. Thermochim. Acta 2018, 669, 169-172.
https://doi.org/10.1016/j.tca.2018.09.022

1069. Kustov A.V., Belykh D.V., Smirnova N.L., Venediktov E.A., Kudayarova T.V., Kruchin S.O., Berezin D.B. Dyes and Pigments 2018, 149, 553-559.
https://doi.org/10.1016/j.dyepig.2017.09.073

1070. Berezin D.B., Kustov A.V., Krestyaninov M.A., Shukhto O.V., Batov D.V., Kukushkina N.V. J. Mol. Liq. 2019, 283, 532-536.
https://doi.org/10.1016/j.molliq.2019.03.091

1071. Kustov A.V., Kustova T.V., Belykh D.V., Khudyaeva I.S., Berezin D.B. Dyes and Pigments 2020, 173, 107948.
https://doi.org/10.1016/j.dyepig.2019.107948

1072. Berezin D.B., Makarov V.V., Znoyko S.A., Mayzlish V.E., Kustov A.V. Mend. Commun. 2020, 30, 621-623.
https://doi.org/10.1016/j.mencom.2020.09.023

1073. Kustov A.V., Belykh D.V., Startseva O.M., Kruchin S.O., Venediktov E.A., Berezin D.B. Pharm. Anal. Acta 2016, 7(5), 480-484.
https://doi.org/10.4172/2153-2435.1000480

1074. Yakavets I., Millard M., Zorin V., Lassalle H.-P., Bezdetnaya L. J. Contr. Release 2019, 304, 268-287.
https://doi.org/10.1016/j.jconrel.2019.05.035

1075. Smith D.A., Van de Waterbeemd H., Walker D.K., Mannhold R., Kubinyi H., Timmerman H. Pharmacokinetics and Metabolism on Drug Design. In: Methods and Principles in Medicinal Chemistry (Mannhold R., Kubinyi H., Timmerman H., Eds.) Weinheim: Wiley-VCH Verlag, 2001. 141 p.

1076. Fromm-Dornieden C., Rembe J.D., Schäfer N., Böhm J., Stuermer E.K. J. Med. Microbiol. 2015, 64(4), 407-414.
https://doi.org/10.1099/jmm.0.000034

1077. Venediktov E.A., Tulikova E.Yu., Rozhkova E.P., Belykh D.V., Khudyaeva I.S., Berezin D.B. Macroheterocycles 2017, 10(3), 295-300.
https://doi.org/10.6060/mhc170404v

1078. Dabrowski J.M. Adv. Inorg. Chem. 2017, 70, 343-394.
https://doi.org/10.1016/bs.adioch.2017.03.002

1079. Schwartzberg L.S., Navari R.M. Adv. Ther. 2018, 35(6), 754-767.
https://doi.org/10.1007/s12325-018-0707-z

1080. Mahmood M.E., Al-Koofee D.A.F. Global J. Sc. Front. Res. Chem. 2013, 13(4), 1-7.

1081. Kustov A.V., Berezin D.B., Koifman O.I. Antimicrobial and Antiviral Photodynamic Therapy: Mechanisms, Targets and Prospects for Clinical Applications. In: Functional Materials Based on Tetrapyrrole Macrocyclic Compounds (Koifman O.I., Ed.) Moscow: Lenand, 2019. p. 532-581. (in Russ.).

1082. Drulis-Kawa Z., Bednarkiewicz A., Bugla G., Stręk W., Doroszkiewicz W. Adv. Clin. Exp. Med. 2006, 15(2), 279-283.

1083. Isakau H.A., Parkhats M.V., Knyukshto V.N., Dzhagarov B.M., Petrov E.P., Petrov P.T. J. Photochem. Photobiol. B: Biol. 2008, 92, 165-174.
https://doi.org/10.1016/j.jphotobiol.2008.06.004

1084. Hamblin M.R., Hasan T. Photochem. Photobiol. Sci. 2004, 3(5), 436-450.
https://doi.org/10.1039/b311900a

1085. Bertoloni G., Rossi F., Valduga G., Jori G., Ali H., van Lier J.E. Microbios 1992, 71(286), 33-46.

1086. Lambrechts S.A.G., Demidova T.N., Aalders M.C.G. Photochem. Photobiol. Sci. 2005, 4, 503.
https://doi.org/10.1039/b502125a

1087. Awad М.М., Tovmasyan A., Craik J.D., Batinic-Haberle I., Benov L.T. Appl. Microbiol. Biotechnol. 2016, 100, 7679-7688.
https://doi.org/10.1007/s00253-016-7632-3

1088. Geynits A.V., Sorokaty A.E., et al. Laser Medicine 2007, 1(3), 45.

1089. Gostishchev V.K. General Surgery. Moscow: GEOTAR-MEDIA, 2016. 736 p.

1090. Briskin B.S., Proshin A.V., Lebedev V.V., Yakobishvili Ya.I. Infections in Surgery 2003, 1(4), 11-1.

1091. Hamblin M.R., Abrahamse H. Antibiotics (Basel) 2020, 9(2), E53.
https://doi.org/10.3390/antibiotics9020053

1092. Hamblin M.R., Dai T. Photodiagnosis Photodyn Ther. 2010, 7(2), 134-136.
https://doi.org/10.1016/j.pdpdt.2010.04.004

1093. Sharma S.K., Dai T., Kharkwal G.B., Huang Y.Y., Huang L., De Arce V.J., Tegos G.P., Hamblin M.R. Curr. Pharm. Des. 2011, 17(13), 1303-1319.
https://doi.org/10.2174/138161211795703735

1094. St Denis T.G., Dai T., Izikson A., Astrakas C., Anderson R.R., Hamblin M.R., Tegos G.P. Virulence 2011, 2(6), 509-520..
https://doi.org/10.4161/viru.2.6.17889

1095. Cacaccio J., Durrani F., Cheruku R.R., Borah B., Ethirajan M., Tabaczynski W., Pera P., Missert J.R., Pandey R.K. Photochem. Photobiol. 2020, 96, 625-635.
https://doi.org/10.1111/php.13183

1096. Jenkins S.V., Srivatsan A., Reynolds K.Y., Gao F., Zhang Y., Heyes C.D., Pandey R.K., Chen J. J. Colloid Interface Sci. 2016, 461, 225-231..
https://doi.org/10.1016/j.jcis.2015.09.037

1097. Srivatsan A., Pera P., Joshi P., Wang Y., Missert J.R., Tracy E.C., Tabaczynski W.A., Yao R., Sajjad M., Baumann H., Pandey R.K. Bioorg. Med. Chem. 2015, 23, 3603-17. PMID 25936263.
https://doi.org/10.1016/j.bmc.2015.04.006

1098. Grandi V., Bacci S., Corsi A., Sessa M., Puliti E., Murciano N., Scavone F., Cappugi P., Pimpinelli N. Photodiagn. Photodyn. Therapy 2018, 21, 252-256.
https://doi.org/10.1016/j.pdpdt.2017.12.012

1099. Akhlyustina E.V. J. Physics: Conf. Series 2019, 1189.
https://doi.org/10.1088/1742-6596/1189/1/012033

1100. Kurochkina A.Yu., Plavsky V.Yu., Yudina N.A. Med. J. 2010, 2, 131-133.

1101. Casas A., Fukuda H., Di Venosa G., Batlle A. Br. J. Cancer 2001, 85(2), 279-284.
https://doi.org/10.1054/bjoc.2001.1875

1102. Zeina B., Greenman J., Corry D., Purcell W.M. Br. J. Dermatol. 2002, 146, 568-573.
https://doi.org/10.1046/j.1365-2133.2002.04623.x

1103. Stranadko E.F., Kuleshov I.Yu., Karakhan G.I. Laser Medicine 2010, 14(2), 52-56.

1104. Shin F.E., Tolstykh P.I., Stranadko E.F., Solovieva A.B., Ivanov A.V., Eliseenko V.I., Mamantov P.G., Shin E.F., Kuleshov I.Yu. Laser Medicine 2009, 3-4, 55-60.

1105. Malik Z., Ladan H., Nitzan Y., Smetana Z. Antimicrobal and Antiviral Activity of Porphyrin Photosensitation. In: Photodynamic Therapy of Cancer (Jori G., Moan J., Star W., Eds.) Proc. SPIE 2078, 1994. p. 305-312.
https://doi.org/10.1117/12.168668

1106. Pаolo L.R., Segalla A., Bertoloni G., et al. J. Photochem. Photobiol. 2000, 59(1-3), 152-158.
https://doi.org/10.1016/S1011-1344(01)00114-2

1107. Kato I.T., Prates R.A., Sabino C.P., Fuchs B.B., Tegos G.P., Mylonakis E., Hamblin M.R., Ribeiro M.S., Antimicrob. Agents Chemother. 2013, 57(1), 445-451.
https://doi.org/10.1128/AAC.01451-12

1108. Jori G., Brown S.B. Photochem. Photobiol. Sci. 2004, 3, 403-405.
https://doi.org/10.1039/b311904c

1109. Dai T., Fuchs B.B., Coleman J.J., Prates R.A., Astrakas C., St. Denis T., Ribeiro M.S., Mylonakis E., Hamblin M.R., Tegos G.P. Front. Microbiol. 2012, 120..
https://doi.org/10.3389/fmicb.2012.00120

1110. Jori J. J. Environ. Path. Toxcol. Oncol. 2006, 25, 505-519.
https://doi.org/10.1615/JEnvironPatholToxicolOncol.v25.i1-2.320

1111. Vera D.M., Haynes M.H., Ball A.R., Dai D.T., Astrakas C., Kelso M.J., Hamblin M.R., Tegos G.P. Photochem. Photobiol. 2012, 88(3), 499-511.
https://doi.org/10.1111/j.1751-1097.2012.01087.x

1112. Wilson B.C. In: Handbook of Photonics for Biomedical Science (Tuchin V.V., Ed.). London: CRC Press, Taylor & Francis Group, 2010. p. 649-686.

1113. Harris F., Pierpoint L. Med. Res. Rev. 2012, 32(6), 1292-327.
https://doi.org/10.1002/med.20251

1114. Li X., Guo H., Tian Q., Zheng G., Hu Y., Fu Y., Tan H. J. Surg. Res. 2013, 184(2), 1013-21.
https://doi.org/10.1016/j.jss.2013.03.094

1115. Wozniak A., Grinholc M. Front Microbiol. 2018, 9, 930.
https://doi.org/10.3389/fmicb.2018.00930

1116. Grinholc M., Nakonieczna J., Fila G., Taraszkiewicz A., Kawiak A., Szewczyk G., Sarna T., Lilge L., Bielawsk K.P. Appl. Microbiol. Biotechnol. 2015, 99(9), 4031-4043.
https://doi.org/10.1007/s00253-015-6539-8

1117. Hamblin M.R. Photochem. Photobiol. 2012, 88(3), 496-8.
https://doi.org/10.1111/j.1751-1097.2012.01139.x

1118. Thota S., Wang M., Jeon S., Maragani S., Hamblin M.R., Chiang L.Y. Molecules 2012, 17(5), 5225-43.
https://doi.org/10.3390/molecules17055225

1119. Malik Z., Hanania J., Nitzan Y. J. Photochem. Photobiol. B 1990, 5, 281-293.
https://doi.org/10.1016/1011-1344(90)85044-W

1120. Stranadko E.F., Koraboev U.M., Tolstykh M.P. Surgery 2000, 9, 67-70.

1121. Lu Z.R., Ye F., Vaidya A. J. Control. Release 2007, 122, 269-277.
https://doi.org/10.1016/j.jconrel.2007.06.016

1122. Knop K., Mingotaud A.-F., El-Akra N., Violleau F., Souchard J.-P. Photochem. Photobiol. Sci. 2009, 8, 396-404.
https://doi.org/10.1039/b811248g

1123. Nitzan Y., Gutterman M., Malik Z., Ehrenberg B. Photochem. Photobiol. 1992, 55(1), 89-96.
https://doi.org/10.1111/j.1751-1097.1992.tb04213.x

1124. Strakhovskaya M.G., Belenikina N.S., Nikitina V.V., Kovalenko S.Yu., Kovalenko I.B., Averyanov A.V., Rubin A.B., Galochkina T.V. Clinical Practice 2013, 4(1), 25-30.
https://doi.org/10.17816/clinpract4125-30

1125. Loke W.K., Lau S.K., Yong L.L., Khor E. Sum C.K. J. Biomed. Mater. Res. 2000, 53(1), 8.
https://doi.org/10.1002/(SICI)1097-4636(2000)53:1<8::AID-JBM2>3.0.CO;2-3

1126. Muzzarelli R.A.A., Morganti P., Morganti G., Palombo P., Palombo M., Biagini G., Belmonte M.M., Giantomassi F., Orlandi F., Muzzarelli C. Carbohydrate Polymers 2007, 70(3), 27434.
https://doi.org/10.1016/j.carbpol.2007.04.008

1127. Aoyagi S., Onishi H., Machida Y. Int. J. Pharm. 2007, 330(1-2), 138-45.
https://doi.org/10.1016/j.ijpharm.2006.09.016

1128. Solak E.K., Kaya S. J. Gazi University Health Sciences 2020, 2(1), 11-17.

1129. Zhientaev T.M., Melik-Nubarov N.S., Litmanovich E.A., Aksenova N.A., Glagolev N.N., Solovieva A.B. Polymer Science, Ser. A 2009, 5, 757-767.

1130. Solovieva А.B., Melik-Nubarov N.S., Zhiyentayev Т.М., Tolstih P.I., Kuleshov I.I., Aksenova N.A., Litmanovich E.A., Glagolev N.N., Timofeeva V.А., Ivanov A.V. Laser Physics 2009, 19(4), 1-8.
https://doi.org/10.1134/S1054660X09040410

1131. Solovieva A.B., Glagolev N.N., Ivanov A.V., Konoplyannikov A.G., Melik-Nubarov N.S., Rogovina S.Z., Zhientaev T.M. An Agent for the Treatment of Malignant tumors by the Method of Photodynamic Therapy, 2008, RF patent No 2314806.

1132. Gorokh Yu.A., Aksenova N.A., Solovieva A.B., Olshevskaya V.A., Zaitsev A.V., Lagutina M.A., Luzgina V.N., Mironov A.F., Kalinin V.N. Russ. J. Phys. Chem., A 2011, 85, 871-875.
https://doi.org/10.1134/S003602441105013X

1133. Solovieva A.B., Tolstykh P.I., Ivanov A.V., Glagolev N.N., Shinn F.E., Kuleshov I.Yu. A Method of Treating Extensive Purulent Wounds of Soft Tissues, 2010, RF patent No 2396994.

1134. Huang L., Xuan Y., Koide Y., Zhiyentayev T., Tanaka M., Hamblin M.R. Lasers Surg. Med. 2012, 44(6), 490-9.
https://doi.org/10.1002/lsm.22045

1135. Wagner J.R., Ali H., Langlois R., Brasseur N., van Lier J.E. Photochem. Photobiol. 1987, 45(5), 587-594.
https://doi.org/10.1111/j.1751-1097.1987.tb07384.x

1136. Aksenova N.A., Oles T., Sarna T., Glagolev N.N., Chernjak A.V., Volkov V.I., Kotova S.L., Melik-Nubarov N.S., Solovieva A.B. Laser Physics 2012, 22(10), 1642-1649.
https://doi.org/10.1134/S1054660X12100015

1137. Solovieva A.B., Tolstih P.I., Melik-Nubarov N.S., Zhientaev T.M., Kuleshov I.G., Glagolev N.N., Ivanov A.V., Karahanov G.I., Tolstih M.P., Timashev P.S. Laser Phyics 2010, 5, 1068-1074.
https://doi.org/10.1134/S1054660X10090203

1138. Aksenova N.A., Zhientaev T.M., Brilkina A.A., Dubasova L.V., Ivanov A.V., Timashev P.S., Melik-Nubarov N.S., Solovieva A.B. Photonics & Lasers in Medicine 2013, 2(3), 189-198.
https://doi.org/10.1515/plm-2013-0011

1139. Zhiyentayev T.M., Boltaev U.T., Solov'eva A.B., Aksenova N.A., Glagolev N.N., Chernjak A.V., Melik-Nubarov N.S. Photochem. Photobiol. 2014, 90, 171-182.
https://doi.org/10.1111/php.12181

1140. Tsvetkov V.B., Solov'eva A.B., Melik-Nubarov N.S. Phys. Chem. Chem. Phys. 2014, 16, 10903-10913.
https://doi.org/10.1039/C3CP55510K

1141. Rudenko T.G., Shekhter A.B., Guller A.E., Aksenova N.A., Glagolev N.N., Ivanov A.V., Aboyants R.K., Kotova S.L., Solovieva A.B. Photochem. Photobiol. 2014, 90, 1413-1422.
https://doi.org/10.1111/php.12340

1142. Solovieva A.B., Kardumian V.V., Aksenova N.A., Belovolova L.V., Glushkov M.V., Bezrukov E.A., Sukhanov R.B., Kotova S.L., Timashev P.S. Sci. Rep. 2018, 8, 8042.
https://doi.org/10.1038/s41598-018-26458-6

1143. Fontana C.R., dos Santos D.S. Jr., Bosco J.M., Spolidorio D.M., Marcantonio R.A. Drug Deliv. 2008, 15(7), 417-422.
https://doi.org/10.1080/10717540802007433

1144. Aksenova N.A., Timofeeva V.A., Rogovina S.Z., Timashev P.S., Glagolev N.N., Solovieva A.B. Polymer Science, Series B 2010, 52(2), 122-128.
https://doi.org/10.1134/S1560090410010100

1145. Glagolev N.N., Rogovina S.Z., Solov'eva A.B., Aksenova N.A., Kotova S.L. Russ. J. Phys. Chem. 2006, 80, Suppl. 1., S72-S76.
https://doi.org/10.1134/S0036024406130127

1146. Kardumyan V.V., Aksenova N.A., Chernyak A.A., Glagolev N.N., Volkov V.I., Solovieva A.B. Laser Phys. 2015, 25(4), 6002.
https://doi.org/10.1088/1054-660X/25/4/046002

1147. Solovieva A.B., Spokoiny A.L., Rudenko T.G., Shekhter A.B., Glagolev N.N., Aksenova N.A. Clinical Practice 2016, 2, 45-49.
https://doi.org/10.17816/clinpract7245-49

1148. Tolstykh P.I., Shin F.E., Tamrazova O.B., Derbenev V.A., Kuleshov I.Yu., Solovieva A.B., Vasyagin S.N. Military Medical J. 2010, 8, 41.

1149. Rushai A.K., Makarenko A.V., Bodachenko K.A., Kolosova T.A. Clinical Medicine 2013, 14(4), 101-104.

1150. Drexler H. Cardiovasc Res. 1999, 43, 572-579.
https://doi.org/10.1016/S0008-6363(99)00152-2

1151. Shumaev K.B., Gubkin A.A., Gubkina S.A., Gudkov L.L., Sviryaeva I.V., Timoshin A.A., Topunov A.F., Vanin A.F., Ruuge E.T.O. Biophysics 2006, 51(3), 472-477.
https://doi.org/10.1134/S0006350906030134

1152. Santos C.X.C., Anilkumar N., Zhang M., Brewer A.C., Shah A.M. Free Radical Biology & Medicine 2011, 50(7), 777-793.
https://doi.org/10.1016/j.freeradbiomed.2011.01.003

1153. Murray J., Taylor S.W., Zhang В., Ghosh S.S., Capaldi R.A. J. Biol. Chem. 2003, 278(39), 37223-37230.
https://doi.org/10.1074/jbc.M305694200

1154. Vanin A.F. Biochemistry 1998, 63, 924-938.

1155. Mironov A.F. Photodynamic Therapy for Cancer. In: Advances in the Chemistry of Porphyrins. Vol. 1. (Golubchikov O.A., Ed.) SPb.: St-PbGU, 1997. p. 357-374

1156. Solovieva A.B., Vanin A.F., Shekhter A.B., Glagolev N.N., Aksenova N.A., Mikoyan V.D., Kotova S.L., Rudenko T.G., Fayzullin A.L., Timashev P.S. Nitric Oxide 2019, 83, 24-32.
https://doi.org/10.1016/j.niox.2018.12.004

1157. Davies A.G. Tin Organometallics. In: Comprehensive Organometallic Chemistry. Vol. 3. London: Elsevier, 2007. p. 809-883.
https://doi.org/10.1016/B0-08-045047-4/00054-6

1158. Desai A., Mitchison T.J. Ann. Rev. Cell. Dev. Biol. 1997, 13, 83-117.
https://doi.org/10.1146/annurev.cellbio.13.1.83

1159. Milaeva E.R., Shpakovsky D.B., Gracheva Y.A., Antonenko T.A., Osolodkin D.I., Palyulin V.A., Shevtsov P.N., Neganova M.E., Vinogradova D.V., Shevtsova E.F. J. Organomet. Chem. 2015, 782, 96-102.
https://doi.org/10.1016/j.jorganchem.2014.12.013

1160. Milaeva E., Petrosyan V., Berberova N., Pimenov Y., Pellerito L. Bioinorg. Chem. Appl. 2004, 18, 69-91.
https://doi.org/10.1155/S1565363304000068

1161. Benedetti M, Giuliani M.E., Regoli F. Ann. NY Acad. Sci. 2015, 1340, 8-19.
https://doi.org/10.1111/nyas.12698

1162. Aschner M., Aschner J.L. Neurosc. Biobehav. Rev. 1992, 16, 427-435.
https://doi.org/10.1016/S0149-7634(05)80184-8

1163. Milaeva E.R., Tyurin V.Yu., Gracheva Yu.A., Dodochova M.A., Pustovalova L.M., Chernyshev V.N. Bioinorg. Chem. Appl. 2006, Article ID 64927, 1-5.
https://doi.org/10.1155/BCA/2006/64927

1164. Tyurin V.Yu., Zhang J., Glukhova A.P., Milaeva E.R. Macroheterocycles 2011, 4, 211-212.
https://doi.org/10.6060/mhc2011.3.10

1165. Milaeva E.R., Tyurin V.Yu., Shpakovsky D.B., Gerasimova O.A., Zhang J., Gracheva Yu.A. Heteroatom Chem. 2006, 17, 475-480.
https://doi.org/10.1002/hc.20269

1166. Forman H.J., Zhang H., Rinna A. Mol. Aspects Med. 2009, 30, 1-12.
https://doi.org/10.1016/j.mam.2008.08.006

1167. Cappellini M.D., Fiorelli G. Lancet 2008, 371, 9606, 64-74.
https://doi.org/10.1016/S0140-6736(08)60073-2

1168. Levy H.R., Christoff M. Biochem J. 1983, 214, 959-965.
https://doi.org/10.1042/bj2140959

1169. Milgrom L.R., Jones C.C., Harriman A. J. Chem. Soc. Perkin Trans. 1988, 2, 71-79.
https://doi.org/10.1039/p29880000071

1170. Gerbec E.N., Messing R.D., Starber S.B. Brain Res. Bull. 1988, 346-351.
https://doi.org/10.1016/0006-8993(88)90379-4

1171. Steckelbroeck S., Stoffel-Wagner B., Reichelt R., Schramm J., Bidlingmaier F., Siekmann L., Klingmuller D. J. Neuroendocrinol. 1999, 11, 457-464.
https://doi.org/10.1046/j.1365-2826.1999.00363.x

1172. Pashkov A.N., Popov S.S., Semenikhina A.V., Rakhmanova T.I. Bull. Experim. Biol. Med. 2005, 139, 520-524.
https://doi.org/10.1007/s10517-005-0346-7

1173. Sedlak J., Lindsey R.H. Anal. Biochem. 1968, 2, 192-205.
https://doi.org/10.1016/0003-2697(68)90092-4

1174. Geloso M.C., Corvino V., Cavallo V., Toesca A., Guadagni E., Passalacqua R., Michetti F. Neurosci. Lett. 2004, 357, 103-107.
https://doi.org/10.1016/j.neulet.2003.11.076

1175. Kook S.C., Wong K., Ng Meng, Kumar Das V.G. Appl. Organomet. Chem. 1991, 5, 409-415.
https://doi.org/10.1002/aoc.590050507

1176. Bosch B.J., van der Zee R., de Haan C.A.M., Rottier P.J.M. J. Virol. 2003, 77, 8801-8811.
https://doi.org/10.1128/JVI.77.16.8801-8811.2003

1177. Lu R., Zhao X., Li J. et al. The Lancet 2020, 395, 565-574.
https://doi.org/10.1016/S0140-6736(20)30251-8

1178. Hoffmann M., Kleine-Weber H., Schroeder S., et al. Cell 2020, 2, 271-280.
https://doi.org/10.1016/j.cell.2020.02.052

1179. Xu X., Chen P., Wang J., Feng J., et al. Science China Life Sciences 2020, 63, 457-460.
https://doi.org/10.1007/s11427-020-1637-5

1180. Wan Y., Shang J., Graham R., et al. J. Virol. 2020, 94, e00127-20.
https://doi.org/10.1128/JVI.00127-20

1181. Zhang H., Penninger J.M., Li Y., Zhong N., Slutsky A.S. Intensive Care Medicine 2020, 46, 586-590.
https://doi.org/10.1007/s00134-020-05985-9

1182. Yan R., Zhang Y., Li Y., Xia L., Guo Y., Zhou Q. Science 2020, 361(6485), 1444-1448.
https://doi.org/10.1126/science.abb2762

1183. Zhao Y., Zhao Z., Wang Y., Zhou Y., Ma Y., Zuo W. Am. J. Respir. Critical Care Med. 2020, 202, 756-759.
https://doi.org/10.1164/rccm.202001-0179LE

1184. Coutard B., Valle C., de Lamballerie X., Canard B., Seidah N.G., Decroly E. Antiviral Res. 2020, 176(104742), 1-5.
https://doi.org/10.1016/j.antiviral.2020.104742

1185. Matsuyama S., Nao N, Shirato K., et al. Proc. Nat. Acad. Sci. USA 2020, 117(13), 7001-7003.
https://doi.org/10.1073/pnas.2002589117

1186. Kawase M., Shirato K., van der Hoek L., Taguchi F., Matsuyama S. J. Virol. 2012, 86(12), 6537-6545.
https://doi.org/10.1128/JVI.00094-12

1187. Zhou Y., Vedantham P., Lu K., et al. Antiviral Res. 2015, 116, 76-84.
https://doi.org/10.1016/j.antiviral.2015.01.011

1188. Kuba K., Imai Y., Rao S., et al. Nat. Med. 2005, 11, 875-879.
https://doi.org/10.1038/nm1267

1189. Monteil V., Kwon H., Prado P., et al. Cell 2020, 181(4), 905-913.
https://doi.org/10.1016/j.cell.2020.04.004

1190. Gheblawi M., Wang K., Viveiros A., et al. Circ. Res. 2020, 126, 1456-1474.
https://doi.org/10.1161/CIRCRESAHA.120.317015

1191. Jiang S., Hillyer C., Du L. Trends in Immunology 2020, 5, 355-359.
https://doi.org/10.1016/j.it.2020.03.007

1192. Wang C., Li W., Drabek D. et al. Nat. Commun. 2020, 11, 2251.
https://doi.org/10.1038/s41467-020-16256-y

1193. Widjaja I., Wang C., Haperen R., et al. Emerg. Microbes Infect. 2019, 8, 516-530.
https://doi.org/10.1080/22221751.2019.1597644

1194. Hwang W.C., Lin Y., Santelli E., et al. J. Biol. Chem. 2006, 281, 34610-34616.
https://doi.org/10.1074/jbc.M603275200

1195. Pedersen S.F., Ho Y.-C. J. Clin. Invest. 2020, 130(5), 2202-2205.
https://doi.org/10.1172/JCI137647

1196. Woo Y.L., Kamarulzaman A., Augustin Y., Staines H., Altice F. J. Petrol. 2020. DOI: 10.31219/osf.io/mxsvw.
https://doi.org/10.31219/osf.io/mxsvw

1197. Bussalino E., Maria A. De, Russo R., et al. Am. J. Transplant. 2020, 7, 1922-1924.
https://doi.org/10.1111/ajt.15920

1198. Sarzi-Puttini P., Giorgi V., Sirotti S., Marotto D., et al. Clinical and Experimental Rheumatology 2020, 38(2), 337-342.

1199. Wu C., Liu Y., Yang Y., et al. Acta Pharm. Sin. B 2020, 10(5), 766-788.
https://doi.org/10.1016/j.apsb.2020.02.008

1200. Smith M., Smith J. ChemRxiv 2020. DOI: 10.26434/chemrxiv.11871402.
https://doi.org/10.26434/chemrxiv.11871402

1201. Lebedeva N., Popova T., Kozbial M., et al. J. Porphyrins Phthalocyanines 2011, 15(4), 223-229.
https://doi.org/10.1142/S1088424611003185

1202. Lebedeva N.S., Gubarev Y.A., Koifman O.I. Mendeleev Commun. 2015, 25, 307-309.
https://doi.org/10.1016/j.mencom.2015.07.027

1203. Lebedeva N., Malkova E., Vyugin A. Koifman O., Gubarev Y. Biochip J. 2016, 10, 1-8.
https://doi.org/10.1007/s13206-016-0101-3

1204. Walls A.C., Park Y.J., Tortorici M.A., et al. Cell 2020, 181(2), 281-292.
https://doi.org/10.1016/j.cell.2020.02.058

1205. Frisch M.J., Trucks G.W., Schlegel H.B., et al. Gaussian Inc., Wallingford 2013, 121, 150-166.

1206. Trott O., Olson A.J. J. Comput. Chem. 2010, 31(2), 455-461.
https://doi.org/10.1002/jcc.21334

1207. Syrbu S.A., Semeikin A.S., Berezin B.D., Koifman O.I. Khimiya Geterociklicheskih Soedineniy 1989, 10, 1373-1377.

1208. Koifman O.I., Ponomarev G.V., Syrbu S.A., Zharov E.V., Sergeeva T.V., Lukovkin A.V., 2014, Patent RF No 2535097.

1209. Kruper W.J., Chamberlin Jr.T.A., Kochanny M. J. Org. Chem. 1989, 11, 2753-2756.
https://doi.org/10.1021/jo00272a057

1210. Sharma K.K., Mandloi M., Rai N., Jain R. RSC Adv. 2016, 6, 96762-96767.
https://doi.org/10.1039/C6RA23364C

1211. van den Tempel N., Horsman M.R., Kanaar R. International Journal of Hyperthermia 2016, 32, 446-454.
https://doi.org/10.3109/02656736.2016.1157216

1212. Mallory M., Gogineni E., Jones G.C., Greer L., Simone II C.B. Crit. Rev. Oncol. Hematol. 2016, 97, 56-64.
https://doi.org/10.1016/j.critrevonc.2015.08.003

1213. Kumar V., Marin-Navarro J., Shukla P. World J. Microbiol. Biotechnol. 2016, 32, 34.
https://doi.org/10.1007/s11274-015-2005-0

1214. Issels R.D., Lindner L.H., Verweij J., Wessalowski R., Reichardt P., Wust P., Ghadjar P., Hohenberger P., Angele M., Salat C. JAMA Oncology 2018, 4, 483-492.
https://doi.org/10.1001/jamaoncol.2017.4996

1215. Cihoric N., Tsikkinis A., van Rhoon G., Crezee H., Aebersold D.M., Bodis S., Beck M., Nadobny J., Budach V., Wust P. International Journal of Hyperthermia 2015, 31, 609-614.
https://doi.org/10.3109/02656736.2015.1040471

1216. Matsumura M., Signor G., Matthews B.W. Nature 1989, 342, 291.
https://doi.org/10.1038/342291a0

1217. Zhang S., Zhang K., Chen X., Chu X., Sun F., Dong Z. Biochem. Biophys. Res. Commun. 2010, 395, 200-206.
https://doi.org/10.1016/j.bbrc.2010.03.159

1218. Joo J.C., Pack S.P., Kim Y.H., Yoo Y.J. J. Biotechnol. 2011, 151, 56-65.
https://doi.org/10.1016/j.jbiotec.2010.10.002

1219. Ahern T.J., Casal J.I., Petsko G.A., Klibanov A.M. Proc. Nat. Acad. Sci. 1987, 84, 675-679.
https://doi.org/10.1073/pnas.84.3.675

1220. Buß O., Rudat J., Ochsenreither K. Comput. Struct. Biotech. J. 2018, 16, 25-33.
https://doi.org/10.1016/j.csbj.2018.01.002

1221. Glick B.R., Pasternak J.J., Patten C.L. Molecular Biotechnology: Principles and Applications of Recombinant DNA, 4th ed, Washington, DS:ASM PRESS, 2010. 1000 p.

1222. Wlodarczyk S.R., Custódio D., Pessoa Jr.A., Monteiro G. Eur. J. Pharm. Biopharm. 2018, 131, 92-98.
https://doi.org/10.1016/j.ejpb.2018.07.019

1223. Fields P.A. Comp. Biochem. Physiol. Part A: Molecular & Integrative Physiology 2001, 129, 417-431.
https://doi.org/10.1016/S1095-6433(00)00359-7

1224. Vieille C., Zeikus G.J. Microbiol. Mol. Biol. Rev. 2001, 65, 1-43.
https://doi.org/10.1128/MMBR.65.1.1-43.2001

1225. Bonch-Osmolovskaya E., Miroshnichenko M., Kostrikina N., Chernych N., Zavarzin G. Arch Microbiol. 1990, 154, 556-559.
https://doi.org/10.1007/BF00248836

1226. Haney P.J., Badger J.H., Buldak G.L., Reich C.I., Woese C.R., Olsen G.J. Proc. Nat. Acad. Sci. 1999, 96, 3578-3583.
https://doi.org/10.1073/pnas.96.7.3578

1227. Chakravarty S., Varadarajan R. FEBS Lett. 2000, 470, 65-69.
https://doi.org/10.1016/S0014-5793(00)01267-9

1228. Empadinhas N., da Costa M.S. Int. Microbiol. 2006, 9(3), 199-206.

1229. Kaur P., Ghai N., Sangha M.K. African J. Biotech. 2009, 8, 619-625.

1230. Bursy J., Kuhlmann A.U., Pittelkow M., Hartmann H., Jebbar M., Pierik A.J., Bremer E. Appl. Environ. Microbiol. 2008, 74, 7286-7296.
https://doi.org/10.1128/AEM.00768-08

1231. Fischer D., Geyer A., Loos E. The FEBS J. 2006, 273, 137-149.
https://doi.org/10.1111/j.1742-4658.2005.05050.x

1232. Faria T.Q., Mingote A., Siopa F., Ventura R., Maycock C., Santos H. Carbohydr. Res. 2008, 343, 3025-3033.
https://doi.org/10.1016/j.carres.2008.08.030

1233. Grigoryan K., Markarian S., Aznauryan M. Problems of Cryobiology and Cryomedicine 2009, 19, 3-10.

1234. Timasheff S.N. Annu. Rev. Biophys. Biomol. Struct. 1993, 22, 67-97.
https://doi.org/10.1146/annurev.bb.22.060193.000435

1235. Timasheff S.N. Biochemistry 2002, 41, 13473-13482.
https://doi.org/10.1021/bi020316e

1236. Liu Y., Bolen D. Biochemistry 1995, 34, 12884-12891.
https://doi.org/10.1021/bi00039a051

1237. Michels J.J., Fiammengo R., Timmerman P., Huskens J., Reinhoudt D.N. J. Inclusion Phenom. Macrocycl. Chem. 2001, 41, 163-172.
https://doi.org/10.1023/A:1014488423489

1238. Raffaini G., Ganazzoli F. J. Inclusion Phenom. Macrocycl. Chem. 2013, 76, 213-221.
https://doi.org/10.1007/s10847-012-0193-x

1239. Arakawa T., Bhat R., Timasheff S.N. Biochemistry 1990, 29, 1914-1923.
https://doi.org/10.1021/bi00459a036

1240. Barone G., Capasso S., Del Vecchio P., De Sena C., Fessas D., Giancola C., Graziano G., Tramonti P. J. Therm. Anal. Calorim. 1995, 45, 1255-1264.
https://doi.org/10.1007/BF02547420

1241. Barone G., Giancola C., Verdoliva A. Thermochim. Acta 1992, 199, 197-205.
https://doi.org/10.1016/0040-6031(92)80263-V

1242. Farruggia B., Rodriguez F., Rigatuso R. J. Protein Chem. 2001, 20, 81-89.
https://doi.org/10.1023/A:1011000317042

1243. Lebedeva N., Malkova E., Gubarev Y., V'yugin A., Borisov A. Int. J. Org. Chem. 2013, 3, 225-228.
https://doi.org/10.4236/ijoc.2013.34031

1244. Wang S.-L., Lin S.-Y., Li M.-J., Wei Y.-S., Hsieh T.-F. Biophys Chem. 2005, 114, 205-212.
https://doi.org/10.1016/j.bpc.2004.12.004

1245. Itoh T., Wada Y., Nakanishi T. Agric. Biol. Chem. 1976, 40, 1083-1086.
https://doi.org/10.1080/00021369.1976.10862172

1246. Baier S.K., McClements D.J. J. Agric. Food Chem. 2003, 51, 8107-8112.
https://doi.org/10.1021/jf034249m

1247. Yamasaki M., Yano H., Aoki K. Int. J. Biol. Macromol. 1991, 13, 322-328.
https://doi.org/10.1016/0141-8130(91)90012-J

1248. Baier S.K., McClements D.J. Food Res Int. 2003, 36, 1081-1087.
https://doi.org/10.1016/j.foodres.2003.09.003

1249. Michnik A. J. Therm. Anal. Calorim. 2003, 71, 509-519.
https://doi.org/10.1023/A:1022851809481

1250. Tankovskaia S.A., Abrosimova K.V., Paston S.V. J. Mol. Struct. 2018, 1171, 243-252.
https://doi.org/10.1016/j.molstruc.2018.05.100

1251. Michnik A., Drzazga Z. J. Therm. Anal. Calorim. 2007, 88, 449-454.
https://doi.org/10.1007/s10973-006-8072-6

1252. Das A., Basak P., Pattanayak R., Kar T., Majumder R., Pal D., Bhattacharya A., Bhattacharyya M., Banik S. P. Int. J. Biol. Macromol. 2017, 105, 645-655.
https://doi.org/10.1016/j.ijbiomac.2017.07.074

1253. Samanta N., Mahanta D.D., Hazra S., Kumar G.S., Mitra R.K. Biochimie 2014, 104, 81-89.
https://doi.org/10.1016/j.biochi.2014.05.009

1254. Baier S., McClements D.J. J. Agric. Food Chem. 2001, 49, 2600-2608.
https://doi.org/10.1021/jf001096j

1255. Platts L., Falconer R.J. Int. J. Pharm. 2015, 486, 131-135.
https://doi.org/10.1016/j.ijpharm.2015.03.051

1256. Shil S., Das N., Sengupta B. Sen P. ACS Omega 2018, 3, 16633-16642.
https://doi.org/10.1021/acsomega.8b01832

1257. Dasgupta M., Kishore N. PloS one 2017, 12, e0172208.
https://doi.org/10.1371/journal.pone.0172208

1258. Lebedeva N.S., Gubarev Y.A., Lyubimtsev A.V., Yurina E.S., Koifman O.I. Macroheterocycles 2017, 10, 37-42.
https://doi.org/10.6060/mhc160530g

1259. Lebedeva N.S., Gubarev Y.A., Yurina E.S., Syrbu S.A. J. Mol. Liq. 2018, 265, 664-667.
https://doi.org/10.1016/j.molliq.2018.06.030

1260. Lebedeva N.S., Malkova E., Popova T., Kutyrev A., Syrbu S., Parfenyuk E., Vyugin A. Spectrochim. Acta Part A: Mol. Biomol. Spectrosc. 2014, 118, 395-398.
https://doi.org/10.1016/j.saa.2013.06.101

1261. Lebedeva N.S., Yurina E.S., Guseinov S.S., Gubarev Y.A, Syrbu S.A. Dyes Pigments 2019, 162, 266-271.
https://doi.org/10.1016/j.dyepig.2018.10.034

Attachment	Size
mhc200814k.pdf	14.02 MB

Журнал "Макрогетероциклы"

Navigation

Languages

News

Search