Liang Yaoyu, Das Uttam Kumar, Luo Jie, Diskin-Posner Yael, Avram Liat, Milstein David
Department of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 7610001, Israel.
Department of Chemical Research Support, Weizmann Institute of Science, Rehovot 7610001, Israel.
J Am Chem Soc. 2022 Oct 19;144(41):19115-19126. doi: 10.1021/jacs.2c08491. Epub 2022 Oct 4.
The development of catalysts for environmentally benign organic transformations is a very active area of research. Most of the catalysts reported so far are based on transition-metal complexes. In recent years, examples of catalysis by main-group metal compounds have been reported. Herein, we report a series of magnesium pincer complexes, which were characterized by NMR and X-ray single-crystal diffraction. Reversible activation of H via aromatization/dearomatization metal-ligand cooperation was studied. Utilizing the obtained complexes, the unprecedented homogeneous main-group metal catalyzed semihydrogenation of alkynes and hydrogenation of alkenes were demonstrated under base-free conditions, affording -alkenes and alkanes as products, respectively, with excellent yields and selectivities. Control experiments and DFT studies reveal the involvement of metal-ligand cooperation in the hydrogenation reactions. This study not only provides a new approach for the semihydrogenation of alkynes and hydrogenation of alkenes catalyzed by magnesium but also offers opportunities for the hydrogenation of other compounds catalyzed by main-group metal complexes.
开发用于环境友好型有机转化的催化剂是一个非常活跃的研究领域。迄今为止报道的大多数催化剂都是基于过渡金属配合物。近年来,已有主族金属化合物催化的实例报道。在此,我们报道了一系列镁钳形配合物,通过核磁共振和X射线单晶衍射对其进行了表征。研究了通过芳构化/去芳构化金属-配体协同作用实现的氢的可逆活化。利用所得到的配合物,在无碱条件下实现了前所未有的均相主族金属催化的炔烃半氢化和烯烃氢化反应,分别以优异的产率和选择性得到了反式烯烃和烷烃产物。对照实验和密度泛函理论研究揭示了金属-配体协同作用参与了氢化反应。该研究不仅为镁催化的炔烃半氢化和烯烃氢化提供了一种新方法,也为其他主族金属配合物催化的化合物氢化提供了机会。