Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
Chemistry. 2023 Jul 11;29(39):e202301034. doi: 10.1002/chem.202301034. Epub 2023 Jun 9.
Electrochemistry offers a sustainable platform for discovering reactions involving single-electron transfer (SET) that generates highly reactive and synthetically versatile radical species. Compared with photochemistry similarly specializing in SET which requires expensive photocatalysts, electrochemistry employs low-cost electricity to drive the electron flow. Paired electrolysis makes use of both half-reactions, thus obviating the need for sacrificial reactions and maximizing the atom and energy economy. In convergent paired electrolysis, anodic oxidation and cathodic reduction occur simultaneously to generate two intermediates, which are then coupled to furnish the product. It represents a distinctive approach to challenging redox-neutral reactions. However, the gap between the two electrodes makes it hard for a reactive intermediate to come across the other coupling partner. This concept article summarizes recent state-of-the-art advances on radical-based convergent paired electrolysis, which adopted different strategies to overcome the difficulty.
电化学提供了一个可持续的平台,用于发现涉及单电子转移(SET)的反应,这些反应会产生高反应性和合成多功能的自由基物种。与专门从事 SET 的光化学相比,电化学利用低成本的电力来驱动电子流动,而光化学同样需要昂贵的光催化剂。成对电解利用两个半反应,从而避免了牺牲反应的需要,并最大限度地提高了原子和能量效率。在收敛的成对电解中,阳极氧化和阴极还原同时发生,生成两个中间体,然后将它们偶联以生成产物。这是一种解决具有挑战性的氧化还原中性反应的独特方法。然而,两个电极之间的间隙使得反应性中间体很难遇到其他偶联伙伴。本文综述了基于自由基的收敛成对电解的最新研究进展,该方法采用了不同的策略来克服这一困难。