A Highly Active Manganese Precatalyst for the Hydrosilylation of Ketones and Esters

被引:132
|
作者
Mukhopadhyay, Tufan K. [1 ]
Flores, Marco [1 ]
Groy, Thomas L. [1 ]
Trovitch, Ryan J. [1 ]
机构
[1] Arizona State Univ, Dept Chem, Tempe, AZ 85287 USA
关键词
CARBONYL-COMPOUNDS; CATALYTIC HYDROSILYLATION; IRON CATALYSTS; COMPLEXES; HYDROSILATION; ALDEHYDES;
D O I
10.1021/ja4116346
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reduction of ((PDI)-P-Ph2PPr)MnCl2 allowed the preparation of the formally zerovalent complex, ((PDI)-P-Ph2PPr)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 ((PDI)-P-Ph2PPr)Mn was found to mediate the atom-efficient utilization of Si-H bonds to form quaternary silane products. ((PDI)-P-Ph2PPr)Mn was also shown to catalyze the dihydrosilylation of esters following cleavage of the substrate acyl C-O bond. Electronic structure investigation of ((PDI)-P-Ph2PPr)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.
引用
收藏
页码:882 / 885
页数:4
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