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Electron-transfer reduction of dinuclear copper peroxo and bis-μ-oxo complexes leading to the catalytic four-electron reduction of dioxygen to water

Title
Electron-transfer reduction of dinuclear copper peroxo and bis-μ-oxo complexes leading to the catalytic four-electron reduction of dioxygen to water
Authors
Tahsini L.Kotani H.Lee Y.-M.Cho J.Nam W.Karlin K.D.Fukuzumi S.
Ewha Authors
남원우조재흥Shunichi Fukuzumi이용민Kenneth D. Karlin
SCOPUS Author ID
남원우scopus; Shunichi Fukuzumiscopus; 이용민scopusscopus
Issue Date
2012
Journal Title
Chemistry - A European Journal
ISSN
0947-6539JCR Link
Citation
vol. 18, no. 4, pp. 1085 - 1093
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
The four-electron reduction of dioxygen by decamethylferrocene (Fc *) to water is efficiently catalyzed by a binuclear copper(II) complex (1) and a mononuclear copper(II) complex (2) in the presence of trifluoroacetic acid in acetone at 298a K. Fast electron transfer from Fc* to 1 and 2 affords the corresponding Cu I complexes, which react at low temperature (193a K) with dioxygen to afford the η 2: η 2-peroxo dicopper(II) (3) and bis-μ-oxo dicopper(III) (4) intermediates, respectively. The rate constants for electron transfer from Fc* and octamethylferrocene (Me 8Fc) to 1 as well as electron transfer from Fc* and Me 8Fc to 3 were determined at various temperatures, leading to activation enthalpies and entropies. The activation entropies of electron transfer from Fc* and Me 8Fc to 1 were determined to be close to zero, as expected for outer-sphere electron-transfer reactions without formation of any intermediates. For electron transfer from Fc* and Me 8Fc to 3, the activation entropies were also found to be close to zero. Such agreement indicates that the η 2: η 2-peroxo complex (3) is directly reduced by Fc* rather than via the conversion to the corresponding bis-μ-oxo complex, followed by the electron-transfer reduction by Fc* leading to the four-electron reduction of dioxygen to water. The bis-μ-oxo species (4) is reduced by Fc* with a much faster rate than the η 2:η 2- peroxo complex (3), but this also leads to the four-electron reduction of dioxygen to water. Catalytic reduction of dioxygen: Two copper complexes that act as efficient catalysts for the four-electron four-proton reduction of O 2 by Fc* in the presence of trifluoroacetic acid in acetone have been prepared and characterized. The roles of the η 2: η 2-peroxo and bis-μ-oxo intermediates in the catalytic four-electron reduction of O 2 to water have been clarified (see figure). Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
DOI
10.1002/chem.201103215
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자연과학대학 > 화학·나노과학전공 > Journal papers
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