Synthesis of Porphyrin-Containing Hydrogels under Microwave Radiation Conditions

Nadezhda L. Pechnikova,^a@ Alexander S. Smirnov,^a Ivan V. Shilov,^a Alexey V. Lyubimtsev,^a Marina N. Mileeva,^b and Tatiana A. Ageeva^a

^aIvanovo State University of Chemistry and Technology, 153000 Ivanovo, Russia

^bIvanovo State Medical Academy, 153012 Ivanovo, Russia

^@Corresponding author E-mail: peclin@mail.ru

DOI: 10.6060/mhc214076p
Macroheterocycles 2021 14(4) 328-333

Dedicated to the memory of Prof. G. V. Ponomarev, Prof. A. F. Mironov and T. S. Kurtikyan

The synthesis of new functional hydrogels on acrylamide and tetra-aryl-substituted porphyrins with N,N’-methylene-bis-acrylamide and the study of their physical and chemical properties are described, the hydrogels being synthesized at different ratios of initial components under microwave conditions. Electron spectroscopy and scanning electron microscopy were used to characterize the hydrogels obtained; their sorption properties being also investigated. Best sorption properties were shown by hydrogels containing mono-meso-allyloxy substituted porphyrin. The values of the gel fraction, the swelling degree and the water content in the hydrogels were established to be significantly affected by the amount of crosslinking agent used in the hydrogels synthesis.

References:

Click here to expand or collapse this section

1. Honey P.J., Rijo J., Anju A., Anoop K.R. Acta Pharmaceutica Sinica B 2014, 4, 120–127.
http://dx.doi.org/10.1016/j.apsb.2014.02.005

2. Chu L.-Y., Xie R., Ju X.-J., Wang W. Smart Hydrogel Functional Materials. Beijing: Chemical Industry Press, 2013. 384 р.
https://doi:10.1007/978-3-642-39538-3

3. Abd Alla S.G., El-Din H.M.N., El-Naggar A.W.M. European Polymer Journal 2007, 43, 2987–2998.
https://doi:10.1016/j.eurpolymj.2007.04.016

4. Cvek M., Zahoranova A., Mrlik M., Sramkova P., Minarik A., Sedlacik M. Colloids and Surfaces B: Biointerfaces 2020, 190, 110912–110921.
https://doi.org/10.1016/j.colsurfb.2020.110912

5. Hu K., Sun J., Guo Z., Wang P., Chen Q., Ma M., Gu N. Advanced Materials 2015, 27, 2507–2514.
https://doi.org/10.1002/adma.201405757

6. Lv F., Mao L., Liu T. Materials Science and Engineering 2014, 43, 221–230.
http://dx.doi.org/10.1016/j.msec.2014.07.019

7. Hernández R., Zamora-Mora V., Sibaja-Ballestero M., Vega-Baudrit J., López D., Mijangos C. Journal of Colloid and Interface Science 2009, 339, 53–59.
https://doi.org/10.1016/j.jcis.2009.07.066

8. Belali S., Karimi R., Hadizadeh M. Polymer 2017, 109, 93–105.
http://dx.doi.org/10.1016/j.polymer.2016.12.041

9. Costa e Silva R., Oliveira da Silva L., Bartolomeu A.A., Brocksom T.J., de Oliveira K.T. Journal of Organic Chemistry 2020, 16, 917–955.
https://doi:10.3762/bjoc.16.83

10. Zhu Yu., Wu H., Fang Z., Yang X., Guo K., He W. Molecular Catalysis 2021, 514, 111765–111775.
https://doi.org/10.1016/j.mcat.2021.111765

11. Zhang Yu., Zhang G.-L., Wang Yu-T., Ma Z., Yang T.-Yi, Zhang T., Zhang Y.-H. Journal of Colloid and Interface Science 2021, 596, 342–351.
https://doi:10.1016/j.jcis.2021.03.104

12. Kobayashi N. Izvestiya Vysshikh Uchebnykh Zavedenii Khimiya Khimicheskaya Tekhnologiya 2019, 62, 4–46.
https://doi:10.6060/ivkkt.20196206.5913_1

13. Koifman O.I., Ageeva T.A. Polymer Science, Series C 2014, 56, 84–103.

14. Koifman O.I., Stuzhin P.A., Travkin V.V., Pakhomov G.L. RSC Advances 2021, 11, 15131–15152.
https://doi:10.1039/d1ra01508g

15. Koifman O.I., Ageeva T.A., Beletskaya I.P. et. al. Macroheterocycles 2020, 13, 311–467.
https://doi:10.6060/mhc200814k

16. Norvaiša K., Kielmann M., Senge M.O. ChemBioChem 2020, 21, 1793–1807.
http://dx.doi.org/10.1002/cbic.202000067

17. Urbani M., Grätzel M., Nazeeruddin M.K., Torres T. Chemical Reviews 2014, 114, 12330–12396.
https://dx.doi.org/10.1021/cr5001964

18. Ryan A.A., Senge M.O. Photochemical & Photobiological Sciences 2015, 14, 638–660.
https://doi:10.1039/C4PP00435C

19. Ethirajan M., Chen Y., Joshi P., Pandey R.K. Chemical Society Reviews 2011, 40, 340–362.
https://doi:10.1039/b915149b

20. Wiehe A., O'Brien J.M., Senge M.O. Photochemical & Photobiological Sciences 2019, 18, 2565–2612.
https://doi:10.1039/C9PP00211A

21. Porphyrins: Spectroscopy, Electrochemistry, Application (Enikolopyan N.S., Ed.), Moscow: Nauka, 1985. 333 p.

22. Mironov A.F. In: Advances in Porphyrin Chemistry (Golubchikov O.A., Ed.), SPb.: NII Khimii SPbGU, 1997. p. 357–374.

23. Reshetnikov A.V., Shvec V.I., Ponomarev G.V. In: Advances in Porphyrin Chemistry (Golubchikov O.A., Ed.) SPb.: NII Khimii SPbGU, 1999. p. 70–114.

24. Jahanban-Esfahlan R., Derakhshankhah H., Haghshenas B., Massoumi B., Abbasian M., Jaymand M. International Journal of Biological Macromolecules 2020, 156, 438–445.
https://doi.org/10.1016/j.ijbiomac.2020.04.074

25. Toropceva A.M., Belogorodskaya A.V., Bondarenko V.M. Laboratory workshop on chemistry and technology of macromolecular compounds. Leningrad: Khimiya, 1972. 416 p.

26. Lyubimova T.V., Glazunov A.V., Syrbu S.A., Semeikin A.S., Bykova V.V., Zharnikova N.V., Anan’eva G.A., Usol’tseva N.V. LiquidCrystalsandTheirApplication, 2010, 1, 23–36.

27. Salnikova M.A., Lubimova T.V., Glazynov A.V., Syrbu S.A., Semeikin A.S., Koifman O.I. Macroheterocycles 2013, 6, 53–58.
https://doi.org/10.6060/mhc130118s

28. Wu N., Yu H., Sun M., Li Z., Zhao F., Ao Y. Chen H. ACS Applied Bio Materials 2020, 3, 721–734.
https://doi:10.1021/acsabm.9b01062

29. Borova S., Tokarev V., Stahlhut P., Luxenhofer R. Colloid and Polymer Science 2020, 298, 1699–1713.
https://doi.org/10.1007/s00396-020-04738-w

30. Wong R.S.H., Ashton M., Dodou K. Pharmaceutics 2015, 7, 305–319.
https://doi:10.3390/pharmaceutics7030305

31. Borisov I.M., Luksha R.S., Rashidova S.T., Ageeva T.A. Russian Journal of General Chemistry 2021, 91, 520–527.
https://doi.org/10.1134/S1070363221030208

32. Borisov I.M., Rashidova S.T., Luksha R.S. Russian Journal of General Chemistry 2021, 91, 554–558.
https://doi.org/10.1134/S1070363221030257

33. Parameswaran G., Mathew B. Advances in Environmental Chemistry 2014, 2014, 394841.
http://dx.doi.org/10.1155/2014/394841

34. Hamri S., Lerari D., Sehailia M., Dali-Youcef B., Bouchaour T., Bachari K. International Journal of Plastics Technology 2018, 22, 247–261.
https://doi.org/10.1007/s12588-018-9224-9

35. Torres-Mapa M.L., Singh M., Simon O., Mapa J.L., Machida M., Günther A., Roth B., Heinemann D., Terakawa M., Heisterkamp A. Sensors 2019, 19, 4333–4347.
https://doi:10.3390/s19194333

36. Mosuela R., Mustafa S., Gould S., Hassanin H. Alany R.G., ElShaer A. Colloids and Surfaces B: Biointerfaces, 2018, 163, 91–99.
https://doi.org/10.1016/j.colsurfb.2017.12.024

37. Beruto D.T., Botter R. Biomaterials 2004, 25, 2877–2883.
https://doi:10.1016/j.biomaterials.2003.09.049

38. Yue Y., Wang X., Wu Q., Han J., Jiang J. Polymers 2019, 11, 1239–1255.
https://doi:10.3390/polym11081239

39. Pechnikova N.L., Shilov I.V., Lyubimtsev A.V., Ageeva T.A. Russian Journal of General Chemistry 2021, 91, 1826–1833.
https://doi.org/10.1134/S1070363221090309

Attachment	Size
mhc214076p.pdf	989.73 KB

Журнал "Макрогетероциклы"

Navigation

Languages

News

Search

Synthesis of Porphyrin-Containing Hydrogels under Microwave Radiation Conditions

References: