Department of Chemistry, the Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, 1088 Xueyuan Road, Shenzhen, 518055, P. R. China.
Chemistry and Chemical Engineering Guangdong Laboratory, Shantou, 515031, P. R. China.
Chemistry. 2023 Feb 10;29(9):e202203189. doi: 10.1002/chem.202203189. Epub 2022 Dec 23.
Arene hydrogenation is the most straightforward method to prepare carbo- and heterocycles. However, the high resonance energy prevents aromatic substrates from hydrogenation. Herein the homogeneous, nucleophilic hydrogenation of less electron-rich arenes and heteroarenes is reported. The Co(P N )H species that has been demonstrated to be a strong hydride donor could deliver a hydride ion to the cyano (hetero)arene substrates. Deuterium labeling experiments supported a Michael-type reaction pathway. Theoretical analyses have been conducted to investigate the hydricity of the catalytically active CoH species and the electrophilicity of the arene substrates. An outlook for the synthesis of more challenging substituted benzenes was proposed based on the in silico modification of the CoH species.
芳氢化为制备碳环和杂环化合物最直接的方法。然而,芳香底物的高共振能阻止其加氢。本文报道了电子较少的芳烃和杂芳烃的均相亲核加氢。已证明具有强氢供体能力的 Co(P N )H 物种可以向氰基(杂)芳基底物提供氢负离子。氘标记实验支持 Michael 型反应途径。进行了理论分析以研究催化活性 CoH 物种的氢化物和亲电性的芳基底物。根据 CoH 物种的计算机模拟修饰,提出了用于合成更具挑战性取代苯的方案。