Abstract
Metal ion-coupled and proton-coupled electron-transfer processes are described for one-electron, two-electron, and four-electron reduction of dioxygen by one-electron reductants, such as ferrocene derivatives, as well as by two-electron reductants, such as NADH analogs with metal complexes. The catalytic mechanism of the four-electron reduction of dioxygen as functional models of cytochrome c oxidases has been clarified based on detailed kinetic study and the detection of intermediates.
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