Kinetics and Mechanistic Study of Permanganate Oxidation of Fluorenone Hydrazone in Alkaline Medium

A. Fawzy, Saleh A. Ahmed, I. Althagafi, M. Morad, K. Khairou
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引用次数: 3

Abstract

The oxidation kinetics of fluorenone hydrazone (FH) using potassium permanganate in alkaline medium were measured at a constant ionic strength of 0.1 mol dm−3 and at 25°C using UV/VIS spectrophotometer. A first-order kinetics has been monitored in the reaction of FH with respect to [permanganate]. Less-than-unit order dependence of the reaction on [FH] and [OH−] was revealed. No pronounced effect on the reaction rate by increasing ionic strength was recorded. Intervention of free radicals was observed in the reaction. The reaction mechanism describing the kinetic results was illustrated which involves formation of 1 : 1 intermediate complex between fluorenone hydrazones and the active species of permanganate. 9H-Fluorenone as the corresponding ketone was found to be the final oxidation product of fluorenone hydrazone as confirmed by GC/MS analysis and FT-IR spectroscopy. The expression rate law for the oxidation reaction was deduced. The reaction constants and mechanism have been evaluated. The activation parameters associated with the rate-limiting step of the reaction, along with the thermodynamic quantities of the equilibrium constants, have been calculated and discussed.
高锰酸盐在碱性介质中氧化芴酮腙的动力学及机理研究
采用紫外/可见分光光度计,在0.1 mol dm−3的恒定离子强度和25℃条件下,测定了高锰酸钾在碱性介质中对氟芴酮腙(FH)的氧化动力学。在FH与[高锰酸盐]的反应中监测了一级动力学。结果表明,[FH]和[OH−]对反应的依赖程度小于单位阶。增加离子强度对反应速率无明显影响。在反应中观察到自由基的干预作用。阐述了氟酮腙与高锰酸盐活性组分之间形成1:1中间配合物的反应机理。经GC/MS分析和FT-IR分析证实,9h -芴酮为芴酮腙的最终氧化产物。推导了氧化反应的表达速率规律。计算了反应常数和反应机理。计算并讨论了与反应限速步骤有关的活化参数,以及平衡常数的热力学量。
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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