Hydrosilylation of Aldehydes and Ketones Catalyzed by Nickel PCP-Pincer Hydride Complexes

被引:220
作者
Chakraborty, Sumit [1 ]
Krause, Jeanette A. [1 ]
Guan, Hairong [1 ]
机构
[1] Univ Cincinnati, Dept Chem, Cincinnati, OH 45221 USA
关键词
CARBON-CARBON BONDS; TETRAKIS(TRIETHYL PHOSPHITE)NICKEL HYDRIDE; TRANSITION-METAL HYDRIDES; C-H ACTIVATION; DONOR ABILITIES; PHOSPHINE-LIGANDS; ETHYLENE OLIGOMERIZATION; HOMOGENEOUS CATALYSIS; DIPHOSPHINE LIGANDS; MECHANISTIC INSIGHT;
D O I
10.1021/om800948f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Nickel PCP-pincer hydride complexes catalyze chemoselective hydrosilylation of C=O bonds of aldehydes and ketones in the presence of other functional groups. The mechanism involves C=O insertion into a nickel-hydrogen bond, followed by cleavage of the newly formed Ni-O bond with a silane.
引用
收藏
页码:582 / 586
页数:5
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