Unusual Water Oxidation Mechanism via a Redox-Active Copper Polypyridyl Complex.

Abstract

To improve Cu-based water oxidation (WO) catalysts, a proper mechanistic understanding of these systems is required. In contrast to other metals, high-oxidation-state metal-oxo species are unlikely intermediates in Cu-catalyzed WO because π donation from the oxo ligand to the Cu center is difficult due to the high number of d electrons of CuII and CuIII. As a consequence, an alternative WO mechanism must take place instead of the typical water nucleophilic attack and the inter- or intramolecular radical-oxo coupling pathways, which were previously proposed for Ru-based catalysts. [CuII(HL)(OTf)2] [HL = Hbbpya = N,N-bis(2,2'-bipyrid-6-yl)amine)] was investigated as a WO catalyst bearing the redox-active HL ligand. The Cu catalyst was found to be active as a WO catalyst at pH 11.5, at which the deprotonated complex [CuII(L-)(H2O)]+ is the predominant species in solution. The overall WO mechanism was found to be initiated by two proton-coupled electron-transfer steps. Kinetically, a first-order dependence in the catalyst, a zeroth-order dependence in the phosphate buffer, a kinetic isotope effect of 1.0, a ΔH⧧ value of 4.49 kcal·mol-1, a ΔS⧧ value of -42.6 cal·mol-1·K-1, and a ΔG⧧ value of 17.2 kcal·mol-1 were found. A computational study supported the formation of a Cu-oxyl intermediate, [CuII(L•)(O•)(H2O)]+. From this intermediate onward, formation of the O-O bond proceeds via a single-electron transfer from an approaching hydroxide ion to the ligand. Throughout the mechanism, the CuII center is proposed to be redox-inactive.