Bis[(3,5-dimethyl-1-pyrazolyl)methyl]ethylamine -: A versatile ligand for complexation in RhI cationic complexes

被引:0
|
作者
Mathieu, R
Esquius, G
Lugan, N
Pons, J
Ros, J
机构
[1] CNRS, Chim Coordinat Lab, F-31077 Toulouse 4, France
[2] Univ Autonoma Barcelona, Dept Quim, Bellaterra 08193, Cerdanyola, Spain
关键词
rhodium; aminopyrazole; hemilabile ligands; cationic complexes;
D O I
暂无
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The bis[(3,5-dimethyl-1-pyrazolyl)methyl]ethylamine ligand (1) reacts with [Rh(COD)(THF)(2)][BF4] leading to [Rh(COD)(1)][BF4] ([2][BF4]) in which 1 is kappa (3) bonded in the solid state. Because of the steric bulk of 1,5-cyclooctadiene, it prefers the kappa (2) mode of bonding in solution. Substitution of 1,5-cyclooctadiene by carbon monoxide generates [3] [BF4] in which 1 is kappa (3) bonded in solution and solid state. Variable temperature NMR spectroscopic studies give evidence of a kappa (3) reversible arrow kappa (2) equilibrium in solution. [3][BF4] is easily decarbonylated to [Rh(CO)(1)][BF4] [4][BF4] in which 1 is kappa (3) bonded; however on bubbling carbon monoxide through, [3][BF4] is regenerated. The single-crystal X-ray structures of [2][BF4], [3][BPh4], and [4][BPh4] are reported.
引用
收藏
页码:2683 / 2688
页数:6
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