Ligand development in the Ni-catalyzed hydrocyanation of alkenes

被引:93
作者
Bini, Laura [1 ]
Muller, Christian [1 ]
Vogt, Dieter [1 ]
机构
[1] Eindhoven Univ Technol, Schuit Inst Catalysis, Lab Homogeneous Catalysis, NL-5600 MB Eindhoven, Netherlands
关键词
REDUCTIVE ELIMINATION; BITE ANGLE; ASYMMETRIC HYDROCYANATION; DIPHOSPHINE LIGANDS; PHOSPHORUS LIGANDS; HYDROGEN-CYANIDE; NICKEL; COMPLEXES; CHEMISTRY; ETHYLENE;
D O I
10.1039/c0cc01452d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The addition of HCN to alkenes is a very useful reaction for the synthesis of functional organic substrates. Industrially the nickel-catalyzed hydrocyanation has gained considerable importance mainly because of the production of adiponitrile in the DuPont process. In this process the hydrocyanation of butadiene is carried out using aryl phosphite-modified nickel catalyst. Since the performance of organo-transition metal complexes is largely determined by the ligand environment of the metal, fundamental understanding and ligand development is of pivotal importance for any progress. This feature article gives an account of the development and application of different mono-and bidentate phosphorus-based ligands in the Ni-catalyzed hydrocyanation reaction of alkenes. Special attention will be paid to the development of insight and understanding of the ligand structural and electronic properties towards the improvement of the catalyst performance in terms of stability, activity, and selectivity.
引用
收藏
页码:8325 / 8334
页数:10
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