Dioxygen Binding, Activation, and Reduction to H2O by Cu Enzymes.

Abstract

Oxygen intermediates in copper enzymes exhibit unique spectroscopic features that reflect novel geometric and electronic structures that are key to reactivity. This perspective will describe: (1) the bonding origin of the unique spectroscopic features of the coupled binuclear copper enzymes and how this overcomes the spin forbiddenness of O2 binding and… (More)
DOI: 10.1021/acs.inorgchem.6b01034

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