铑(III)催化铈(IV)在酸性水介质中氧化邻二醇

P. Tandon, Shaista Z. Khanam, S. Singh
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引用次数: 8

摘要

研究了氯化铑在硫酸水溶液中催化邻苯二醇氧化的电位,以及氯化铑催化铈与丙烷-1,2-二醇和丁烷-2,3-二醇反应的动力学。数据表明,对于低浓度的铈(IV),反应遵循一级动力学,但氧化剂浓度的进一步增加会减慢反应速度。反应速率与低浓度的二醇成正比,当有机底物浓度较高时,二醇趋于零级。反应速率在催化剂中为一级反应。氢离子和铈离子浓度的增加对反应速率有阻滞作用,氯离子浓度的增加和介质离子强度的增加对反应速率有正向影响。化学计量学和光谱研究证实,在丙烷-1,2-二醇和丁烷-2,3-二醇的氧化产物中,甲醛和乙醛各形成一个分子,乙醛各形成两个分子。计算了活化焓、活化自由能和熵值等热力学参数,发现丁烷-2,3-二醇比丙烷-1,2-二醇更容易形成活化配合物。
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Oxidation of Vicinal Diols by Cerium(IV) in Aqueous Acidic Media Catalyzed by Rhodium(III)
Potential of rhodium(III) chloride in catalyzing, in aqueous sulfuric acid medium, the oxidation of vicinal diols, and the kinetics of reaction of cerium(IV) with propane-1,2-diol and butane-2,3-diol catalyzed by rhodium(III) chloride was investigated. Data show that the reactions follow first order kinetics with respect to low cerium(IV) for lower concentrations, but a further increase in the oxidant concentration retards the reaction velocity. The reaction rate shows direct proportionality with respect to low concentrations of diol, which tends to become zero order at higher concentrations of the organic substrate. The Rate is first order in catalyst. Increase in the concentrations of hydrogen and cerium(III) ions show retarding effects while increase in chloride ion concentration and in turn ionic strength of the medium has a positive effect on the rate. Stoichiometry and spectral studies confirmed the formation of one molecule each of formaldehyde and acetaldehyde and two molecules of acetaldehyde as the products of oxidation in case of propane-1,2- diol and butane-2,3-diol respectively. Thermodynamic parameters like enthalpy of activation, free energy of activation and entropy values were calculated and it was found that the formation of activated complex in the case of butane-2,3-diol was easy compared to that in the case of propane-1,2-diol.
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