Department of Chemistry and Biochemistry, Arizona State University , Tempe, Arizona 85287, United States.
J Am Chem Soc. 2014 Jan 22;136(3):882-5. doi: 10.1021/ja4116346. Epub 2014 Jan 10.
The reduction of ((Ph2PPr)PDI)MnCl2 allowed the preparation of the formally zerovalent complex, ((Ph2PPr)PDI)Mn, which features a pentadentate bis(imino)pyridine chelate. This complex is a highly active precatalyst for the hydrosilylation of ketones, exhibiting TOFs of up to 76,800 h(-1) in the absence of solvent. Loadings as low as 0.01 mol % were employed, and ((Ph2PPr)PDI)Mn was found to mediate the atom-efficient utilization of Si-H bonds to form quaternary silane products. ((Ph2PPr)PDI)Mn was also shown to catalyze the dihydrosilylation of esters following cleavage of the substrate acyl C-O bond. Electronic structure investigation of ((Ph2PPr)PDI)Mn revealed that this complex possesses an unpaired electron on the metal center, rendering it likely that catalysis takes place following electron transfer to the incoming carbonyl substituent.
((Ph2PPr)PDI)MnCl2 的还原允许制备形式上的零价配合物 ((Ph2PPr)PDI)Mn,其具有五齿双(亚氨基)吡啶螯合配体。该配合物是酮的氢硅烷化的高效前催化剂,在没有溶剂的情况下,其 TOF 高达 76800 h-1。使用的负载量低至 0.01 mol%,并且发现 ((Ph2PPr)PDI)Mn 介导了 Si-H 键的原子经济利用,形成了季硅烷产物。((Ph2PPr)PDI)Mn 还被证明可以在底物酰基 C-O 键断裂后催化酯的二氢硅烷化。对 ((Ph2PPr)PDI)Mn 的电子结构研究表明,该配合物在金属中心具有未成对电子,这表明催化作用可能发生在向进入的羰基取代基进行电子转移之后。