Orthometalation of Tp*Rh(PPh3)2: Implications for Catalytic Reactivity
作者
Changsheng Cao,Tongen Wang,Brian O. Patrick,Jennifer A. Love
出处
期刊:Organometallics [American Chemical Society] 日期:2006-02-01卷期号:25 (5): 1321-1324被引量:14
标识
DOI:10.1021/om0510268
摘要
In the course of our studies of the catalytic reactivity of Tp*Rh(PPh 3 ) 2 ( 1 ), we noted considerable decomposition of 1 in reactions conducted in 1,2-dicholoroethane (DCE) requiring extended reaction times (>12 h). Because this decomposition could have significant implications for the catalytic utility of 1, we have undertaken a study of the decomposition process. We herein report that 1 undergoes facile, irreversible orthometalation of a PPh 3 ligand at room temperature in slightly polar solvents, such as THF and 1,2-dichloroethane. In comparison, orthometalation is virtually undetectable in PhCH 3 at room temperature. Fortunately, 1 shows catalytic activity for hydrothiolation and hydrophosphinylation in low-polarity solvents. Accordingly, reactions using 1 (and potentially related complexes) should be conducted in nonpolar solvents or solvent mixtures whenever possible.