Inner Sphere Reduction of Tris(pyridine-2- carboxylato)manganese(III) by Hydroxylammonium Ion in Sodium Picolinate-Picolinic Acid Buffer Media

K. Gupta, B. Pal
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引用次数: 1

Abstract

Abstract The kinetics and mechanism of the oxidation of hydroxylamine by tris(pyridine-2-carboxylato)manganese( III) in Na(pic)-picH [where Na( pic) = sodium salt of pyridine-2-carboxylic acid (picH)] has been studied in the pH range 4.89-6.10. The rate of the reaction increases with increasing [substrate] but with decreasing acidity. A rate expression has been derived from which the dissociation constant of the equilibrium NH3OH+ ⇄ NH2OH + H+ has been computed at different temperatures. Activation parameters for the slow rate determining step have been evaluated. Manganese(III) complex is reduced by the hydroxylammonium ion by an inner sphere mechanism. The reaction appears to proceed through the intermediate formation of free radicals to give products of oxidation.
羟基铵离子在吡啶酸钠-吡啶酸缓冲介质中内球还原三(吡啶-2-羧酸)锰(III)
摘要研究了pH为4.89 ~ 6.10范围内,三(吡啶-2-羧酸)锰(III)在Na(pic)-picH[其中Na(pic) =吡啶-2-羧酸钠盐[picH]中氧化羟胺的动力学和机理。反应速率随[底物]的增加而增加,但随酸度的降低而增加。我们导出了一个速率表达式,由此计算了不同温度下平衡态NH3OH+ NH2OH + H+的解离常数。对慢速决定步骤的激活参数进行了评估。锰(III)配合物通过内球机制被羟铵离子还原。这个反应似乎是通过自由基的中间形成来产生氧化产物的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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