15004-88-3Relevant articles and documents
A reaction mechanism for oxidative addition of halogen to platinum(II), reductive elimination of halide from platinum(IV) and halide assisted anations of platinum(IV) complexes
Elding,Gustafson
, p. 165 - 171 (2008/10/09)
The oxidative addition of iodine to Pt(CN)42- is first-order with respect to iodide, iodine and complex. The reverse reductive elimination of iodide from trans-Pt(CN)4I22- is first-order with respect to iodide and Pt(CN)4I22-. The kinetics for the reaction between bromide and trans-Pt(CN)4ClH2O2- involves a rate-determining reductive elimination of chloride, followed by a rapid oxidative addition of bromine to the formed Pt(CN)42-. The reactions between trans-Pt(CN)4BrH2O- and bromide or chloride can be described as halide assisted anations. The rate constant for the bromide anation is kexp = k′[Br-]2 and for the chloride anation (in the presence of bromide) k′[Br-][Cl-] + k′' [Cl-]2. All reactions were followed using a stopped-flow technique at 25°C in 0.50M perchloric acid medium. The equilibrium constant for the redox equilibrium between Pt(CN)42-, iodine and Pt(CN)4I22- was determined separately to be (1.29 ± 0.03) × 104M-1. Exploratory stopped-flow experiments indicate that the oxidative addition of chlorine to PtCl22- is first-order with respect to both chlorine and tetrachloroplatinate. The experimental rate laws can be described by a reaction mechanism which resembles that introduced previously for Pt(II)-catalyzed anations and substitutions, in that both mechanisms can be considered as oxidative additions/reductive eliminations.
