Zou Long, Sun Rui, Tao Yongsheng, Wang Xiaofan, Zheng Xinyue, Lu Qingquan
The Institute for Advanced Studies (IAS), Wuhan University, Wuhan, Hubei, P. R. China.
Nat Commun. 2024 Jun 19;15(1):5245. doi: 10.1038/s41467-024-49557-7.
The simultaneous activation of reactants on the anode and cathode via paired electrocatalysis has not been extensively demonstrated. This report presents a paired oxidative and reductive catalysis based on earth-abundant iron/nickel cocatalyzed C-C functionalization of ubiquitous alcohols. A variety of alcohols (i.e., primary, secondary, tertiary, or unstrained cyclic alcohols) can be activated at very low oxidation potential of (~0.30 V vs. Ag/AgCl) via photoelectrocatalysis coupled with versatile electrophiles. This reactivity yields a wide range of structurally diverse molecules with broad functional group compatibility (more than 50 examples).
通过配对电催化同时激活阳极和阴极上的反应物尚未得到广泛证明。本报告提出了一种基于地球上储量丰富的铁/镍共催化普遍存在的醇类进行C-C官能化的配对氧化和还原催化方法。通过光催化与多种亲电试剂耦合,各种醇类(即伯醇、仲醇、叔醇或无张力环醇)可以在非常低的氧化电位(相对于Ag/AgCl约为0.30 V)下被激活。这种反应性产生了广泛的结构多样的分子,具有广泛的官能团兼容性(超过50个实例)。