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ISSN 1998-9539

Porphyrins

The Antioxidant Properties of Asymmetrically Substituted Tetra(meso-aryl)porphyrins with One Phenolic Substituent: The Contribution of Phenol and Porphyrin Fragments to Antioxidant Activity

T. K. Rocheva,a O. G. Shevchenko,b L. I. Mazaletskaya,с N. I. Sheludchenko,с and D. V. Belykha@
aInstitute of Chemistry, Komi Scientific Center, Ural Division, Russian Academy of Sciences, 167000 Syktyvkar, Russia
bInstitute of Biology, Komi Scientific Center, Ural Division, Russian Academy of Sciences, 167982 Syktyvkar, Russia
cEmanuel Institute of Biochemical Physics,Russian Academy of Sciences, 119334 Moscow, Russia

Influence of New N-Methylquinolinyl Porphyrins on Different Candida albicans Development Forms

Mariya Yu. Rusakova,a@ Olga V. Ruschak,b Sergey V. Vodzinskiy,c and Yuriy V. Ishkovc
aBiotechnological Scientific-Education Center, I.I. Mechnikov Odessa National University, 65082 Odessa, Ukraine
Microbiology, Virology and Biotechnology Department, I.I. Mechnikov Odessa National University, 65082 Odessa, Ukraine
cProblem Scientific-Research Laboratory, I.I. Mechnikov Odessa National University, 65082 Odessa, Ukraine

Supramolecular Regioselectivity of meso-Phenylporphyrin Sulfonation. Synthesis of 5,10,15-Tris(4’-sulfophenyl)porphine

Vladimir B. Sheinin,a@ Dmitriy A. Ivanov,a and Oscar I. Koifmana,b
Dedicated to Academician Aslan Yusupovich Tsivadze on the occasion of his Birthday
aG.A. Krestov Institute of Solution Chemistry of Russian Academy of Sciences, 153045 Ivanovo, Russia
bIvanovo State University of Chemistry and Technology, 153000 Ivanovo, Russia
@Corresponding author E-mail: vbs@isc-ras.ru
 

Luminescence Features of Neodymium(III) Compounds with Various Tetrapyrrole Macrocycles

Nikolay N. Semenishyn,a Sergii S. Smola,a Natalya V. Rusakova,a@ Gerbert L. Kamalov,a Yulia G. Gorbunova,b,c and Aslan Yu. Tsivadzeb,c
aA.V. Bogatsky Physico-Chemical Institute, 65080 Odessa, Ukraine
bA.N. Frumkin Institute of Physical Chemistry and Electrochemistry of Russian Academy of Sciences, 119071 Moscow,
Russia

Attempts of the Synthesis of Highly Functionalized Porphyrins at the β-Positions: Nitration of Exhaustively Substituted Moieties in the ’Eastern Half ’ and Mass-Spectral Study of the Reaction Products

Sylwia Ostrysz, Agnieszka Mikus, and Stanislaw Ostrowski@
Institute of Chemistry, Uniwersytet Przyrodniczo-Humanistyczny w Siedlcach, 08-110 Siedlce, Poland
@Corresponding author E-mail: stan@uph.edu.pl
 
DOI: 10.6060/mhc170405o
Macroheterocycles 2017 10(3) 323-327
 

Spectral-Luminescent Properties of meso-Tetraarylporphyrins Revisited: The Role of Aryl Type, Substitution Pattern and Macrocycle Core Protonation

Irina V. Vershilovskaya,a Stefano Stefani,b Pieter Verstappen,c Thien H. Ngo,b,d@1 Ivan G. Scheblykin,e Wim Dehaen,f Wouter Maes,c@2 and Mikalai M. Kruka@3
aBelarussian State Technological University, Physics Department, 220006 Minsk, Belarus
bInstitut für Chemie und Biochemie, Freie Universität Berlin, 14195 Berlin, Germany

Electrochemical Characterization of β-Alkyl Substituted Porphyrins and Mn(III) Complexes in Alkaline Solution

Nadezhda M. Berezina,a@ Maria E. Klueva,b and Mikhail I. Bazanova
aIvanovo State University of Chemistry and Technology, Research Institute of Macroheterocyclic Compounds,
153000 Ivanovo, Russia
bIvanovo State Medical Academy of the Ministry of Healthcare of the Russian Federation, 153000 Ivanovo, Russia
@Corresponding author E-mail: sky_berezina@rambler.ru
 

Photosensitizers Based on Bacteriopurpurinimide Derivatives and Silica Nanoparticles: Synthesis and Photophysical Properties

Mikhail A. Grin,a Ivan V. Pantiushenko,a Anton V. Lobanov,b,c@ Igor A. Mikhaylov,c Nataliya B. Sultimova,d Petr P. Levin,d Petr V. Ostroverkhov,a Alexander G. Majouga,e,f Mikhail Ya. Melnikov,e and Andrey F. Mironova
aMoscow Technological University, 119571 Moscow, Russia
bSemenov Institute of Chemical Physics, Russian Academy of Sciences, 119334 Moscow, Russia

Synthesis, Spectral, Luminescence and Photochemical Properties of the Chlorin е6 Tricationic Derivative with Trimethylammonio Groups

Evgenii A. Venediktov,a@ Elena Yu. Tulikova,a Ekaterina P. Rozhkova,a,b Irina S. Khudyaeva,c Dmitry V. Belykh,с and Dmitry B. Berezinb
aKrestov Institute of Solution Chemistry of Russian Academy of Sciences, 153045 Ivanovo, Russian Federation
bIvanovo State University of Chemistry and Technology, Research Institute of Macroheterocyclic Compounds, 153000 Ivanovo, Russian Federation

Flexible Amide-Bonded Zn(II) Porphyrin Dimer: Electronic Structure Investigation and Its Induced Chirality

Mingfeng Qin,a Minzhi Li,a Weihua Zhu,a@1 Li Xu,a and Xu Lianga,b@2
aSchool of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, P. R. China
bState Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210000, P. R. China
@1Corresponding author E-mail: sayman@ujs.edu.cn