Stable catalyst for intermolecular Pauson-Khand reaction

被引:9
|
作者
Arias, JL
Cabrera, A
Sharma, P
Rosas, N
Sampere, R
机构
[1] Univ Nacl Autonoma Mexico, Fac Estudios Super Cuautitlan, Mexico City, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Quim, Mexico City 04510, DF, Mexico
关键词
Pauson-Khand reaction; homogeneous catalysis; octacarbonyl dicobalt; phosphine modified catalysts; cyclocarbonylation;
D O I
10.1016/j.molcata.2005.11.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The catalytic activity of previously formed Co-2(CO)(6)[P(Ph)(3)](2) (1) was compared with Co-2(CO)(8) and the system formed by Co-2(CO)(8) plus PPh3 in the intermolecular Pauson-Khand (PK) reaction between norbornadiene and phenylacetylene. The effects of pressure, catalyst concentration and temperature were also studied. Additionally, the catalytic activity of complex I was compared with Co-2(CO)(6)[P(OPh)(3)](2) (2) in the intermolecular PK reaction between strained alkenes and terminal and non-terminal afkynes. Both catalysts are very stable, quite efficient and interestingly complex 2 leads to double PK reaction. The results indicate that these complexes are attractive alternatives to Co-2(CO)(8) as catalyst and in addition, complex 2 is an alternative catalyst for double cyclocarbortylation reaction. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:237 / 241
页数:5
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