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追踪水中水氧化过程中的铁(氧)中间体。

Tracking an Fe (O) Intermediate for Water Oxidation in Water.

作者信息

Wei Xiang-Zhu, Ding Tian-Yu, Wang Yang, Yang Bing, Yang Qing-Qing, Ye Shengfa, Tung Chen-Ho, Wu Li-Zhu

机构信息

Key Laboratory of Photochemical Conversion and Optoelectronic Materials, New Cornerstone Science Laboratory, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, P. R. China.

School of Future Technology, University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2023 Sep 4;62(36):e202308192. doi: 10.1002/anie.202308192. Epub 2023 Jul 24.

Abstract

High-valent iron-oxo species are appealing for conducting O-O bond formation for water oxidation reactions. However, their high reactivity poses a great challenge to the dissection of their chemical transformations. Herein, we introduce an electron-rich and oxidation-resistant ligand, 2-[(2,2'-bipyridin)-6-yl]propan-2-ol to stabilize such fleeting intermediates. Advanced spectroscopies and electrochemical studies demonstrate a high-valent Fe (O) species formation in water. Combining kinetic and oxygen isotope labelling experiments and organic reactions indicates that the Fe (O) species is responsible for O-O bond formation via water nucleophilic attack under the real catalytic water oxidation conditions.

摘要

高价铁氧物种对于水氧化反应中进行氧-氧键的形成很有吸引力。然而,它们的高反应活性对剖析其化学转化过程构成了巨大挑战。在此,我们引入一种富电子且抗氧化的配体,2-[(2,2'-联吡啶)-6-基]丙-2-醇来稳定此类转瞬即逝的中间体。先进的光谱学和电化学研究表明在水中形成了高价铁(氧)物种。结合动力学和氧同位素标记实验以及有机反应表明,在实际催化水氧化条件下,铁(氧)物种通过水的亲核进攻负责氧-氧键的形成。

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