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ISSN 1998-9539


Pyropheophorbide-Fullerene Dyad: Synthesis and Photochemical Properties

Alexander Yu. Rybkin,a@ Alexandra Yu. Belik,a Pavel A. Tarakanov,a,c Kamil R. Taziev,b,a Alexei V. Kozlov,a Nikolay S. Goryachev,a,b Ilya V. Sulimenkov,d Viatcheslav I. Kozlovskiy,d,c Yulia V. Romanenko,e Oscar I. Koifman,e and Alexander I. Kotelnikova,b

aInstitute of Problems of Chemical Physics RAS, 142432 Chernogolovka, Russia

bLomonosov Moscow State University, 119991 Moscow, Russia

Tumor Acidic Microenvironment Targeted Pyropheophorbide a Dimer, an Alternative Strategy for Simultaneous Tumor Fluorescence Imaging and PDT Treatment

Lei Cao,a Shisheng Wang,a Liu Wang,a Xiuhan Guo,a Guangzhe Li,a and Weijie Zhaoa,b@ 

aSchool of Pharmaceutical Science and Technology, Dalian University of Technology, 116024 Dalian, P.R. China

bState Key Laboratory of Fine Chemicals, Dalian University of Technology, 116024 Dalian, P.R. China

Electrodeposition and Characterization of Polyporphyrin Films Based on Mn-Complexes of Amino-substituted Tetraphenylporphyrins

Vladimir I. Parfenyuk,a,b@ Mariya V. Tesakova,a Svetlana A. Chulovskaya,a and Sergey M. Kuzmina,c

aG.A. Krestov Institute of Solution Chemistry of RAS, 153045 Ivanovo, Russia

bIvanovo State University of Chemistry and Technology, 153000 Ivanovo, Russia

cIvanovo State Power Engineering University, 153003 Ivanovo, Russia

@Correspondingauthor E-mail:


DOI: 10.6060/mhc190232p

Copper Сomplexes of Сhlorin Derivatives of Chlorophyll a as Potential Photosensitizers for Medical Purposes

D.V. Belykh,a@1 A.S. Kozlov,b Y.I. Pylina,c I.S. Khudyaeva,a А.S. Benditkis,b A.A. Krasnovskyb@2

aInstitute of Chemistry of Komi Scientific Centre of the Ural Branch of the Russian Academy of Sciences, 167000 Syktyvkar, Russia

bFederal Research Centre “Fundamentals of Biotechnology” of the Russian Academy of Sciences, 119071 Moscow, , Russia

Bio-Inspired Ni(II) Porphyrin Dimers with a Bridging Diphenyl Moiety: Facile Synthesis and Molecular Inherent Chirality

Xu Liang,a,b@1 Honglin Zhang,a He Luo,a Mingfeng Qin,a,b Minzhi Li,a and Weihua Zhua,b@2

aSchool of Chemistry and Chemical Engineering, Jiangsu University, 212013 Zhenjiang, P. R. China

bState Key Laboratory of Coordination Chemistry, Nanjing University, 210000 Nanjing, P. R. China

@1Corresponding author E-mail:

Molecular Structure and Conformation of Free Base Corroles

Mikalai M. Kruk,a@1 Dmitry V. Klenitsky,a and Wouter Maesb@2

aBelarusian State Technological University, Physics Department, 220006 Minsk, Belarus

bDesign & Synthesis of Organic Semiconductors (DSOS), Institute for Materials Research (IMO-IMOMEC), Hasselt University, B-3590 Diepenbeek, Belgium

@1Corresponding author E-mail:;

Synthesis and Acid-base Properties of Isomeric Tetrachlorooctabromo- and Tetrabromooctachlorotetraphenylporphyrins

Nugzar Zh. Mamardashvili,@ Yulia B. Ivanova, and Natalya V. Chizhova

G.A. Krestov Institute of Solution Chemistry, Russian Academy of Sciences, 153045 Ivanovo, Russian Federation



DOI: 10.6060/mhc180900m

Macroheterocycles 2019 12(1) 22-28


Excited States Relaxation in Covalently Linked Dyads and Triads Based on Tryptophan, Deuteroporphyrin and Naphthoquinone

Eduard I. Zenkevich,a@ Ekaterina A. Larkina,b Nadezhda V. Konovalova,b and Alexander P. Stupakc

aNational Technical University of Belarus, 220013 Minsk, Belarus

bMIREA – Russian Technological University, M.V. Lomonosov Institute of Fine Chemical Technologies, 119571 Moscow, Russia

cB.I. Stepanov Institute of Physics NAS B, 220072 Minsk, Belarus

@Corresponding author E-mail:


Supramolecular Iron(III) Tetramesitylporphyrin Cluster Structure Assembled by Hydrogen Bonding with Sulfuric Acid

Evgeny V. Kudrik,a,b Sergey E. Nefedov,c@1 and Alexander B. Sorokina@2

aInstitut de Recherches sur la Catalyse et l’Environnement de Lyon (IRCELYON), 69626 Villeurbanne Cedex, France

bInstitut of Macroheterocyclic Compounds, Ivanovo State University of Chemical Technology, 153000 Ivanovo, Russia

cKurnakov Institute of General and Inorganic Chemistry, Russian Academy of Science, 119991 Moscow, Russia

Shielding Effects in 1H NMR Spectra of Halogen-Substituted meso-Tetraphenylporphyrin Derivatives

Stanisław Ostrowski,a@ Beata Łopuszyńska,b and Agnieszka Mikusa


aFaculty of Chemistry, Warsaw University of Technology, 00-664 Warszawa, Poland

bInstitute of Chemistry, Uniwersytet Przyrodniczo-Humanistyczny w Siedlcach, 08-110 Siedlce, Poland

@Corresponding author E-mail:


DOI: 10.6060/mhc181217o

Macroheterocycles 2019 12(1) 17-21