z-logo
Premium
Efficient Reduction of Dioxygen with Ferrocene Catalyzed by Thiocarbohydrazone Tetranuclear Cobalt(III) Coordination Compound
Author(s) -
Kamyabi Mohammad Ali,
Alirezaei Fariba,
SoleymaniBonoti Fatemeh,
Bikas Rahman,
Siczek Milosz,
Lis Tadeusz
Publication year - 2020
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.5833
Subject(s) - chemistry , cobalt , ferrocene , catalysis , ligand (biochemistry) , electron transfer , cyclic voltammetry , coordination complex , crystal structure , crystallography , oxygen , medicinal chemistry , inorganic chemistry , electrochemistry , stereochemistry , photochemistry , metal , organic chemistry , electrode , biochemistry , receptor
The synthesis, characterization and crystal structure of a tetranuclear cobalt(III) coordination compound, [Co 4 (L) 4 ](HSO 4 ) 2 (SO 4 )·4.1(CH 3 OH)·H 2 O ( 1 ), with thiocarbohydrazone based ligand is reported. This compound can efficiently catalyze the reduction of oxygen (O 2 ) by a weak electron donor ferrocene, (Fc), at the polarized water/dichloroethane interface which was investigated by voltammetry and biphasic shake‐flask experiments. Compound 1 contains four cobalt cores which are connected together by sulphur atoms. By having four cobalt cores this coordination compound provides a multi‐electron transfer system for oxygen reduction reactions. The results also suggest that compound 1 catalyzes decomposition of H 2 O 2 at the interface.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom