Haake Matthieu, Reuillard Bertrand, Chavarot-Kerlidou Murielle, Costentin Cyrille, Artero Vincent
Univ. Grenoble. Alpes, CNRS, CEA, IRIG, L, aboratoire de Chimie et Biologie des Métaux, 38000, Grenoble, France.
Département de Chimie Moléculaire, Univ. Grenoble. Alpes, CNRS, 38000, Grenoble, France.
Angew Chem Int Ed Engl. 2024 Dec 20;63(52):e202413910. doi: 10.1002/anie.202413910. Epub 2024 Nov 18.
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 H 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.
参与小分子活化的金属酶的活性位点通常含有作为质子中继体的侧基,这些侧基促进质子耦合电子转移过程。在这里,我们聚焦于氢化酶及其催化的反应,即析氢反应和氧化反应。在简要介绍这些酶之后,我们综述了一些含有质子中继体的各种仿生和受生物启发的分子体系。然后,我们提供了解析此类质子中继体在增强单向催化中关键作用所需的形式电化学框架,并讨论了少数有析氢活性且有定量动力学数据的体系。我们最后强调实现双向催化(同时催化析氢和氢氧化)进而过渡到可逆催化(在狭窄电位范围内催化两个反应)所需的关键参数,并举例说明文献中少数体系的这些特征。