Abstract
The equilibrium coefficient, K1, for the reaction [PdCl4]2- + RR′ SO ⇆ [Pd(RR′ SO)Cl]− + Cl−, has been determined for dimethylsulfoxide, tetramethylensulfoxide, and phenylmethylsulfoxide and found to be 67, 46 and 8.8 respectively at 25°C, ü= 1.0 in 95:5 methanol-water. Values for the equilibrium constants for the dimethylsulfoxide complex are also reported at other ionic strengths. The equilibrium constants for the second stage, [Pd(Me2SO)Cl3]- + Me2SO)⇆-[Pd(Me2SO)2Cl2] + Cl−, has been determined for dimethylsulfoxide only, K2=2.5 × 10−2 at 25°C (μ not controlled). The causes of the mutual destabilisation of two dimethylsulfoxides are discussed.