Regulating proton-coupled electron transfer for efficient water splitting by manganese oxides at neutral pH

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Abstract

Manganese oxides have been extensively investigated as model systems for the oxygen-evolving complex of photosystem II. However, most bioinspired catalysts are inefficient at neutral pH and functional similarity to the oxygen-evolving complex has been rarely achieved with manganese. Here we report the regulation of proton-coupled electron transfer involved in water oxidation by manganese oxides. Pyridine and its derivatives, which have pK a values intermediate to the water ligand bound to manganese(II) and manganese(III), are used as proton-coupled electron transfer induction reagents. The induction of concerted proton-coupled electron transfer is demonstrated by the detection of deuterium kinetic isotope effects and compliance of the reactions with the libido rule. Although proton-coupled electron transfer regulation is essential for the facial redox change of manganese in photosystem II, most manganese oxides impair these regulatory mechanisms. Thus, the present findings may provide a new design rationale for functional analogues of the oxygen-evolving complex for efficient water splitting at neutral pH. © 2014 Macmillan Publishers Limited. All rights reserved.

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Yamaguchi, A., Inuzuka, R., Takashima, T., Hayashi, T., Hashimoto, K., & Nakamura, R. (2014). Regulating proton-coupled electron transfer for efficient water splitting by manganese oxides at neutral pH. Nature Communications, 5. https://doi.org/10.1038/ncomms5256

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