腈
钴
化学
电催化剂
催化作用
氢化物
质子化
组合化学
氧化还原
动力学同位素效应
氢
光化学
氘
无机化学
电化学
有机化学
电极
物理化学
物理
离子
量子力学
作者
Tiantian Wang,Fengjiao He,Wei Jiang,Jie Liu
标识
DOI:10.1002/anie.202316140
摘要
Catalytic hydrogenation of nitriles represents an efficient and sustainable one-step synthesis of valuable bulk and fine chemicals. We report herein a molecular cobalt electrocatalyst for selective hydrogenative coupling of nitriles with amines using protons as the hydrogen source. The key to success for this reductive reaction is the use of an electrocatalytic approach for efficient cobalt-hydride generation through a sequence of cathodic reduction and protonation. As only electrons (e- ) and protons (H+ ) as the redox equivalent and hydrogen source, this general electrohydrogenation protocol is showcased by highly selective and straightforward synthesis of various functionalized and structurally diverse amines, as well as deuterium isotope labeling applications. Mechanistic studies reveal that the electrogenerated cobalt-hydride transfer to nitrile process is the rate-determining step.
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