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ISSN 1998-9539

Porphyrins

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: liangxu@ujs.edu.cn

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: krukmikalai@yahoo.com; m.kruk@belstu.by

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

@CorrespondingauthorE-mail: ngm@isc-ras.ru

 

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: zenkev@tut.by

 

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: stan@ch.pw.edu.pl

 

DOI: 10.6060/mhc181217o

Macroheterocycles 2019 12(1) 17-21

 

The Reactions of Oxotitanium(IV) Tetraphenylporphyrin with Methyl Methacrylate Radicals: A DFT Study

Anna K. Friesen
Ufa Institute of Chemistry - Subdivision of the Ufa Federal Research Centre of the Russian Academy of Sciences, 450054 Ufa, Russia
 
DOI: 10.6060/mhc181112f
Macroheterocycles 2018 11(4) 371-377
 

Evaluation for in vitro Photodynamic Activity of Chlorin e6-Artesunate Conjugates by Irradiation with Different Wavelengths of Light Source

Xiuhan Guo,a,b Yueqing Li,a Shisheng Wang,a,b@ Liu Wang,a Rui Cai,c Guangzhe Li,a and Weijie Zhaoa,b
aSchool of Pharmaceutical Science and Technology, Dalian University of Technology, 116023 Dalian, P. R. China
bState Key Laboratory of Fine Chemicals, Dalian University of Technology, 116023 Dalian, P. R. China
cSchool of Chemical Engineering, Dalian University of Technology, 116023 Dalian, P. R. China

Features of Inverted Tetrasulfophenylporphyrin Protonation. Crucial Role of Hydrogen Bonds

Vladimir B. Sheinin,a@ Olga M. Kulikova,a and Oscar I. Koifmana,b
aG.A. Krestov Institute of Solution Chemistry of the 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
 
DOI: 10.6060/mhc181109s
Macroheterocycles 2018 11(4) 363-370

Advances in the Synthesis of Porphyrin-Fullerenes

Viktoriya S. Lebedeva,a@ Nadezhda A. Mironova,a Ramzes D. Ruziev,b and Andrey F. Mironov a
aMIREA-Russian Technological University, 119454 Moscow, Russian Federation
bScientific Centre for Expert Evaluation of Medicinal Products, 127051 Moscow, Russian Federation
@Corresponding author E-mail: phsstr@gmail.com
 
DOI: 10.6060/mhc180690l