Outside Back Cover: Multisite Proton-Coupled Electron Transfer Facilitates Oxidative Photocatalysis in a Molecular Zr-Based Coordination Compound (Angew. Chem. 38/2025)

Mercedes Moreno-Albarracín, Alvaro M. Rodriguez-Jimenez, Omar Nuñez, Pablo Garrido-Barros
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引用次数: 0

Abstract

Harnessing multisite proton-coupled electron transfer (PCET) through deprotonation of a photoactive Zr coordination cage unlocks oxidative photocatalysis of strong C─H and O─H bonds. This reactivity overcomes the energetic barrier that renders electron transfer alone inaccessible. The Zr platform acts as an ambipolar mediator that unites oxidative and reductive PCET pathways, each operating through distinct mechanisms, and offers new insights for sustainable solar-to-chemical energy conversion, as reported by Pablo Garrido-Barros et al. in their Communication (e202510723).

Abstract Image

外封底:多位点质子耦合电子转移促进了分子zr基配位化合物的氧化光催化(新)。化学38/2025)
利用多位点质子耦合电子转移(PCET),通过光活性Zr配位笼的去质子化,解锁强C─H和O─H键的氧化光催化。这种反应性克服了使电子转移难以实现的能量障碍。正如Pablo Garrido-Barros等人在他们的通讯(e202510723)中所报道的那样,Zr平台作为一种双极性介质,将氧化和还原PCET途径结合在一起,每种途径都通过不同的机制运作,并为可持续的太阳能到化学能转换提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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