Proton Relays in Molecular Catalysis for Hydrogen Evolution and Oxidation: Lessons From the Mimicry of Hydrogenases and Electrochemical Kinetic Analyses

Matthieu Haake, Dr. Bertrand Reuillard, Dr. Murielle Chavarot-Kerlidou, Prof. Cyrille Costentin, Dr. Vincent Artero
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Abstract

The active sites of metalloenzymes involved in small molecules activation often contain pendant bases that act as proton relay promoting proton-coupled electron-transfer processes. Here we focus on hydrogenases and on the reactions they catalyze, i. e. the hydrogen evolution and oxidation reactions. After a short description of these enzymes, we review some of the various biomimetic and bioinspired molecular systems that contain proton relays. We then provide the formal electrochemical framework required to decipher the key role of such proton relay to enhance catalysis in a single direction and discuss the few systems active for H2 evolution for which quantitative kinetic data are available. We finally highlight key parameters required to reach bidirectional catalysis (both hydrogen evolution and hydrogen oxidation catalyzed) and then transition to reversible catalysis (both reactions catalyzed in a narrow potential range) as well as illustrate these features on few systems from the literature.

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质子继电器在氢演化和氧化分子催化中的应用:来自氢化酶模拟和电化学动力学分析的启示
参与小分子活化的金属酶的活性位点通常含有悬垂碱基,它们作为质子继电器促进质子耦合电子转移过程。在这里,我们主要关注氢化酶及其催化的反应。析氢和氧化反应。在简要介绍了这些酶之后,我们回顾了一些包含质子继电器的各种仿生和生物启发分子系统。然后,我们提供了正式的电化学框架,以破译这种质子继电器在单一方向上增强催化作用的关键作用,并讨论了几个对H2演化有活性的系统,这些系统有定量动力学数据可用。我们最后强调了达到双向催化(氢析和氢氧化催化)然后过渡到可逆催化(两种反应都在狭窄的电位范围内催化)所需的关键参数,并从文献中说明了几个系统的这些特征。
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Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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