Lee Mi-Young, Kahl Christian, Kaeffer Nicolas, Leitner Walter
Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, 45470 Mülheim an der Ruhr, Germany.
JACS Au. 2022 Feb 22;2(3):573-578. doi: 10.1021/jacsau.1c00574. eCollection 2022 Mar 28.
Electrifying the production of base and fine chemicals calls for the development of electrocatalytic methodologies for these transformations. We show here that the semihydrogenation of alkynes, an important transformation in organic synthesis, is electrocatalyzed at room temperature by a simple complex of earth-abundant nickel, [Ni(bpy)]. The approach operates under mild conditions and is selective toward the semihydrogenated olefins with good to very good isomer stereoselectivity. (Spectro)electrochemistry supports that the electrocatalytic cycle is initiated in an atypical manner with a nickelacyclopropene complex, which upon further protonation is converted into a putative cationic Ni(II)-vinyl intermediate that produces the olefin after electron-proton uptake. This work establishes a proof of concept for homogeneous electrocatalysis applied to alkyne semihydrogenation, with opportunities to improve the yields and stereoselectivity.
实现基础化学品和精细化学品生产的电气化需要开发用于这些转化的电催化方法。我们在此表明,炔烃的半氢化反应是有机合成中的一个重要转化反应,在室温下可由一种简单的、富含地球元素的镍配合物[Ni(bpy)]进行电催化。该方法在温和条件下运行,对半氢化烯烃具有选择性,具有良好到非常好的异构体立体选择性。(光谱)电化学表明,电催化循环以一种非典型方式由镍环丙烯配合物引发,该配合物在进一步质子化后转化为假定的阳离子Ni(II)-乙烯基中间体,该中间体在吸收电子-质子后生成烯烃。这项工作为应用于炔烃半氢化的均相电催化建立了概念验证,有机会提高产率和立体选择性。