scholarly journals Synthesis of Bis{meso-Tetrakis(4-N-alkylpyridiniumyl)porphyrinato}cerium and Its Redox Switching Behavior

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 790
Author(s):  
Toshio Nishino ◽  
Yasuyuki Yamada ◽  
Ayumi Yamamoto ◽  
Kentaro Tanaka

A novel double-decker porphyrin complex, bis{meso-tetrakis(4-N-alkylpyridiniumyl)porphyrinato}cerium, was prepared. Electrochemical measurements revealed that this complex exhibited reversible redox waves corresponding to a 1e– redox reaction of the cerium center. Treating the complex alternately with an oxidant and a reductant resulted in the reversible redox switching between the oxidized and reduced states in an organic solvent.

2018 ◽  
Vol 256 ◽  
pp. 107-116 ◽  
Author(s):  
Ping Chen ◽  
Aiwu Zhao ◽  
Jin Wang ◽  
Qinye He ◽  
Henghui Sun ◽  
...  

Author(s):  
Manlin Fu ◽  
Kai Wang ◽  
Qiancheng Ma ◽  
Mianli Bian ◽  
Qing Zhu

Abnormal changes in intracellular viscosity and cysteine are both associated with several important biological processes such as reversible redox reaction, which plays a pivotal role in the process of inflammation....


2019 ◽  
Vol 21 (21) ◽  
pp. 11079-11086 ◽  
Author(s):  
C. Karthika ◽  
S. R. Sarath Kumar ◽  
L. Kathuria ◽  
P. K. Das ◽  
A. G. Samuelson

Reversible redox switching of first hyperpolarizability of Monometallic and bimetallic complex.


2018 ◽  
Vol 9 (23) ◽  
pp. 5178-5182 ◽  
Author(s):  
Xiaodan Huang ◽  
Yang Liu ◽  
Chao Liu ◽  
Jun Zhang ◽  
Owen Noonan ◽  
...  

An aluminum–selenium battery powered by the reversible redox reaction of Se/Se2Cl2 has been developed for the first time.


2011 ◽  
Vol 40 (43) ◽  
pp. 11571 ◽  
Author(s):  
Ganngam Phaomei ◽  
R. S. Ningthoujam ◽  
W. Rameshwor Singh ◽  
Romeo Singh Loitongbam ◽  
Naorem Shanta Singh ◽  
...  

2007 ◽  
Vol 11 (05) ◽  
pp. 390-396 ◽  
Author(s):  
Jonathan P. Hill ◽  
Katsuhiko Ariga ◽  
Amy Lea Schumacher ◽  
Paul A. Karr ◽  
Francis D'Souza

5,10,15,20-tetrakis(3,5-di-tert-butyl-4-oxocyclohexadien-2,5-yl)porphyrinogen was alkylated at its macrocyclic nitrogen atoms with pyren-1-ylmethyl groups and the effect of increasing N-substitution on the spectroscopic and electrochemical properties was investigated. Both pyrene and oxoporphyrinogen chromophores exhibit fluorescence and there is little interaction between them except in the higher N-substituted compounds. Intra- or intermolecular excimer formation by pyrene is precluded by attachment to the bulky oxoporphyrinogen. Electrochemical measurements revealed reversible redox behavior.


Sign in / Sign up

Export Citation Format

Share Document