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The anations of Pt(H2O)42+ and PtX(H2O)3+ (to trans-PtX(H2O)2) by X− = Cl−, Br−, I− and SCN− and the anation of trans-PtX2(H2O)2) by X− = Cl−, Br− and I− have been studied at 25 °C and 1.00 M perchlorate medium using both stopped-flow and conventional spectrophotometry. For large excess of X−, PtX42− is formed according to the mechanism in Figure 1. The results indicate an entering ligand order of
