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光电化学铁/镍共催化醇的碳-碳官能化反应

Photoelectrochemical Fe/Ni cocatalyzed C-C functionalization of alcohols.

作者信息

Zou Long, Sun Rui, Tao Yongsheng, Wang Xiaofan, Zheng Xinyue, Lu Qingquan

机构信息

The Institute for Advanced Studies (IAS), Wuhan University, Wuhan, Hubei, P. R. China.

出版信息

Nat Commun. 2024 Jun 19;15(1):5245. doi: 10.1038/s41467-024-49557-7.

Abstract

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).

摘要

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)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf67/11187109/4a7f961eb704/41467_2024_49557_Fig1_HTML.jpg

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