Bis[(3,5-dimethyl-1-pyrazolyl)methyl]ethylamine - A versatile ligand for complexation in Rh-I cationic complexes
Citation
R. Mathieu et al., Bis[(3,5-dimethyl-1-pyrazolyl)methyl]ethylamine - A versatile ligand for complexation in Rh-I cationic complexes, EUR J INORG, (10), 2001, pp. 2683-2688
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
SICI code
1434-1948(200110):10<2683:B-AVLF>2.0.ZU;2-2
Abstract
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 i
s kappa (3) bonded in the solid state. Because of the steric bulk of 1,5-cy
clooctadiene, it prefers the kappa (2) mode of bonding in solution. Substit
ution of 1,5-cyclooctadiene by carbon monoxide generates [3] [BF4] in which
1 is kappa (3) bonded in solution and solid state. Variable temperature NM
R 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 carbo
n monoxide through, [3][BF4] is regenerated. The single-crystal X-ray struc
tures of [2][BF4], [3][BPh4], and [4][BPh4] are reported.