高碘酸离子在水介质中氧化三乙四胺六乙酸钴酸盐(II)配合物的动力学及机理

R. Naik, A. Srivastava, A. Verma, S. Yadav, Ruchi Singh, S. Prasad
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引用次数: 0

摘要

研究了高碘酸盐在酸性水介质中氧化[Co(II)TTHA]4-(其中TTHA =三乙基四胺六乙酸)的动力学和机理。在伪一阶条件下,在λmn = 550 nm处,用大量过量的氧化剂[IO4-]在pH = 4.0 + 0.02, 1 = 0.1 M (CH3COONa + Na NO3)下,在150℃、200℃和250℃三种不同温度下,对[Co(II)TTHA]4-与[IO4-]服从球内反应途径,形成长寿命的中间配合物,最终转化为相应的[Co(III)TTHA]3-配合物作为最终反应产物。实验观察表明,该反应在[Co(II)TTHA]4-中表现出一阶依赖性。当[IO4-]保持其他反应变量不变时,拟一阶速率常数(Kabc)的变化符合以下经验方程:Kabc = a[IO4-]2/b + c[IO4-]此速率规律符合三步机制方案。(Kabc)的值随着pH的增加几乎不变,这是由于[Co(II)TTHA]4-络合物的去质子化形式与[IO4-]在整个pH区域内发生了反应。采用Eyring方程计算活化参数:∆H* = 16.63 KJ mol -1;∆S* = -214.00 JK-1摩尔-1。这些值与提出的三步机制方案一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Kinetics and Mechanism of Oxidation of Triethylenetetraaminehexaacetatocobaltate(II) Complex by Periodate Ion in AqueousMedium
The kinetics and mechanism of oxidation of [Co(II)TTHA]4- (where TTHA = Triehylenetetraaminehexaaceticacid) by periodate ion has been studied in aqueous acidic medium. The reaction has been investigated spectrophotometrically at λmn = 550 nm under pseudo first- order condition by taking large excess of oxidant, [IO4-] at pH = 4.0 + 0.02, 1 = 0.1 M (CH3COONa + Na NO3) and at three different temperatures viz 150 C, 200 C and 250 C. The electron transfer reaction between [Co(II)TTHA]4- and , [IO4-] obeys inner- sphere reaction pathway through the formation of long lived intermediate complex which eventually get converted into a corresponding [Co(III)TTHA]3- complex as final reaction product. The experimental observations have shown that the reaction exhibit first- order dependence in [Co(II)TTHA]4- . The variation of pseudo- first- order rate constant (Kabc) with [IO4-] keeping other reaction variables fixed at constant value is found to obey the following empirical equation. Kabc = a[IO4-]2/b + c[IO4-] This rate law is consistent with a three step mechanistic scheme. The values of (Kabc) are almost invariant with increasing pH and attributed due to the reaction of deprotonated form of [Co(II)TTHA]4- complex and [IO4-] in the whole pH region. Eyring’s equations has been used to calculate the activation parameters and found to be ∆H* = 16.63 KJ mole-1 ; ∆S* = -214.00 JK-1 mole-1. These values are consistent with three step mechanistic scheme as proposed.
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