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首页> 外文期刊>Journal of the Indian Chemical Society >Oxidation studies of formic and oxalic acids by morpholinium fluorochromate : Kinetic and mechanistic study
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Oxidation studies of formic and oxalic acids by morpholinium fluorochromate : Kinetic and mechanistic study

机译:氟铬酸吗啉鎓氧化甲酸和草酸的动力学和机理研究

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摘要

Kinetics and mechanism of oxidation of formic and oxalic acids by morpholinium fluorochromate (MFC) have been studied in dimethylsulphoxide. The main product of oxidation is carbon dioxide. The reaction is first order with respect to MFC. Michaelis-Menten type of kinetics were observed with respect to the reductants. The reaction is acid-catalysed and the acid dependence has the form : k(obs) = a + b[H+]. The oxidation of alpha-deuterioformic acid exhibits a substantial primary kinetic isotope effect (k(H)/k(D) = 5.30 at 298 K). The reaction has been studied in nineteen different organic solvents and the solvent effect has been analysed using Taft's and Swain's multiparametric equations. The temperature dependence of the kinetic isotope effect indicates the presence of a symmetrical cyclic transition state in the rate-determining step. Suitable mechanisms have been proposed.
机译:在二甲基亚砜中研究了吗啉鎓氟铬酸盐(MFC)氧化甲酸和草酸的动力学和机理。氧化的主要产物是二氧化碳。对于MFC,反应是一阶的。关于还原剂,观察到了Michaelis-Menten类型的动力学。该反应是酸催化的,并且酸依赖性具有以下形式:k(obs)= a + b [H +]。 α-氘代甲酸的氧化反应显示出基本的一级动力学同位素效应(在298 K时k(H)/ k(D)= 5.30)。已在19种不同的有机溶剂中研究了该反应,并使用塔夫脱(Taft)和斯文(Swain)多参数方程分析了溶剂的作用。动力学同位素效应的温度依赖性表明在速率确定步骤中存在对称的循环过渡态。已经提出了合适的机制。

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