Perez Jose Fernando Carbajal, Kirlin Fallyn L, Reynolds Eamon F, Altomare-Jarczyk Cole E, Joseph Benjamin T, Keith Jason M, Chianese Anthony R
Department of Chemistry, Colgate University, 13 Oak Drive, Hamilton, New York 13346, United States.
ACS Catal. 2024 Oct 23;14(21):16497-16507. doi: 10.1021/acscatal.4c04475. eCollection 2024 Nov 1.
In this article, we describe a detailed experimental and computational study of the activation mechanism for a highly active pincer ruthenium(0) precatalyst for the hydrogenation of polar organic compounds. The precatalyst activates by reaction with 2 equiv of hydrogen, resulting in a net oxidative addition to ruthenium and hydrogenation of an imine functional group on the supporting ligand. The kinetics of precatalyst hydrogenation were measured by UV-visible spectroscopy under catalytically relevant conditions (10-39 bar hydrogen, 298 K). The kinetic data, in combination with density functional theory calculations, support an intriguing autocatalytic mechanism, where the product ruthenium(II) complex catalyzes the hydrogenation of the ruthenium(0) precatalyst.
在本文中,我们描述了一项针对用于极性有机化合物氢化反应的高活性钳形钌(0)预催化剂活化机制的详细实验和计算研究。该预催化剂通过与2当量的氢气反应而活化,导致钌发生净氧化加成反应以及支撑配体上的亚胺官能团氢化。在催化相关条件(氢气压力10 - 39巴,温度298K)下,通过紫外可见光谱法测定了预催化剂氢化的动力学。动力学数据与密度泛函理论计算相结合,支持了一种有趣的自催化机制,即产物钌(II)配合物催化钌(0)预催化剂的氢化反应。