Hydrogen Carbonate Inhibited and Induced Substitution Reactions of Labile Square-Planar Diethylenetriaminepalladium(II) Complexes

Ernst Breet, Rudi van Eldik
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引用次数: 4

Abstract

The reaction of labile square-planar diethylenetriaminepalladium(II) complexes with hydrogen carbonate ion was studied by stopped flow spectrophotometry as a function of [HCO3] and [Cl] and constant [Pd], ionic strength and temperature to investigate the substitution behaviour with a nucleophile capable of affecting the solution pH. The kinetic results significantly deviate from those for normal square-planar substitution behaviour. The reaction comprises two consecutive equilibrations, which have complex kinetics compared to the simple two-term rate law normally encountered, and which represent hydrogen carbonate inhibited and induced substitution reactions, respectively. The suggested mechanism and data treatment account for the observed deviating kinetics and provide alternative ways of obtaining formerly determined aquation and anation rate constants with comparable accuracy, even for complexes too labile to be monitored directly.

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碳酸氢抑制和诱导不稳定方平面二乙烯三胺钯配合物的取代反应
采用停流分光光度法研究了不稳定的方形平面二乙基三胺钯(II)配合物与碳酸氢离子的反应,研究了[HCO−3]和[Cl−]与恒定的[Pd]、离子强度和温度的函数关系,考察了亲核试剂对溶液ph的取代行为。该反应包括两个连续的平衡,与通常遇到的简单的两项速率定律相比,它们具有复杂的动力学,分别代表碳酸氢抑制和诱导取代反应。所建议的机制和数据处理解释了所观察到的偏离动力学,并提供了以相当精度获得先前确定的水化和气化速率常数的替代方法,即使对于太不稳定而无法直接监测的配合物也是如此。
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