Wang Tiantian, He Fangfang, Jiang Wei, Liu Jie
College of Chemistry and Chemical Engineering, State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, 410082, Changsha, China.
Greater Bay Area Institute for Innovation, Hunan University, 511300, Guangzhou, Guangdong Province, China.
Angew Chem Int Ed Engl. 2024 Feb 12;63(7):e202316140. doi: 10.1002/anie.202316140. Epub 2024 Jan 10.
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.
腈的催化氢化是一种高效且可持续的一步法合成重要大宗化学品和精细化学品的方法。我们在此报告一种分子钴电催化剂,用于使用质子作为氢源,将腈与胺进行选择性氢化偶联。该还原反应成功的关键在于采用电催化方法,通过一系列阴极还原和质子化反应高效生成钴氢化物。由于仅使用电子(e⁻)和质子(H⁺)作为氧化还原当量和氢源,这种通用的电氢化方案通过各种功能化和结构多样的胺的高选择性和直接合成以及氘同位素标记应用得到了展示。机理研究表明,电生成的钴氢化物转移到腈的过程是速率决定步骤。