Kinetic and Mechanistic Pathway of Electron Transfer Reactions: Pyridine Oxidation by Peroxomonophosphoric Acid in Acidic Aqueous Medium

A. Agarwal, A. Meena
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Abstract

The kinetic and mechanistic pathways of pyridine oxidation by peroxomonophosphate has been studied in an acidic aqueous medium. Reactions of peroxomonophosphoric acid are the least exploited kinetically. This reaction has been attempted to understand the role of oxidation of pyridine and the reactivity pattern of peroxomonophosphate. The reaction has been second-order or first-order concerning the oxidant and substrate, respectively. The reaction rate showed a decreasing effect with increasing hydrogen ion concentration. Considering peroxomonophosphate reactions as non-chain reactions and all the results, a feasible mechanism for the reaction has been suggested. The calculated energy of activation and entropy of activation has been observed conventionally to be 80 ± 5 kJ mol-1 and – 45 ± 6 JK-1 mol-1 . The oxidation product was pyridine-N-oxide in this reaction.
电子转移反应的动力学和机理途径:过氧单磷酸在酸性水介质中氧化吡啶
在酸性水介质中研究了过磷酸氧化吡啶的动力学和机理途径。过磷酸单磷酸的反应在动力学上是利用最少的。为了了解吡啶氧化的作用以及过氧单磷酸的反应模式,我们尝试了这一反应。随着氢离子浓度的增加,反应速率呈下降趋势。考虑到过磷酸单胞菌反应为非链反应以及所有结果,提出了该反应的可行机理。计算得出的活化能和活化熵分别为 80 ± 5 kJmol-1 和 - 45 ± 6 JK-1 mol-1。该反应的氧化产物为吡啶-N-氧化物。
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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