期刊
CHEMICAL COMMUNICATIONS
卷 55, 期 38, 页码 5483-5486出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc00971j
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资金
- DST (SERB) of India [YSS/2015/000878]
The electrocatalytic water oxidation activity of a copper(ii) complex, 1, [Cu(L1H)(L-1)(OH2)](ClO4), with a redox active aryl oxime ligand, L1H [L1H = 1-(pyridin-2-yl) ethanone oxime] has been investigated. Complex 1 shows a remarkably high turnover frequency of approximate to 100 s(-1) in neutral phosphate buffer at about 675 mV overpotential with approximate to 94% faradaic efficiency. Electrochemical analysis suggests the involvement of a ligand moiety in a proton-coupled-electron-transfer (PCET) step during the catalytic cycle of complex 1, which in turn provides a route for accumulation of high oxidizing equivalents at the reaction center.
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