Cooxidation of Dibenzalacetone with Oxalic Acid by Pyrazinium Chlorochromate

S. K. Periyasamy, R. Ponmadasamy
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Abstract

Oxidation of dibenzalacetone with pyrazinium chlorochromate in presence of oxalic acid has been studied at 313 K. Various reaction parameters such as effect of varying oxidant, substrate, Hydrogen ion concentration, catalyst, solvent composition, ionic strength, effect of Mn2+, effect of Al3+ and effect of temperature were studied to determine the kinetics of the reaction. Our study revealed that the reaction followed first order dependence with respect to oxidant and catalyst. The reaction followed fractional order kinetics with respect to substrate and H+. Increase in ionic strength was found to have no effect on the reaction rate and decrease in the dielectric constant of the medium decreases the reaction rate. Increase in the concentration of manganous sulphate retarded the reaction rate which confirmed the two-electron transfer involved in the mechanism. There was no possibility of free radical mechanism, which was confirmed by the addition of acrylonitrile shows no significant effect on the reaction rate indicating the non-involvement of free radical reaction.. Based on the experimental observations a mechanism and rate law has been derived. Moreover, the oxidation product was found to be chalcone epoxide, which was characterized by IR spectrum.
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氯铬酸吡嗪与草酸共氧化二苯甲丙酮
研究了草酸存在下吡嗪氯铬酸盐在313k下氧化二苯甲丙酮。考察了氧化剂、底物、氢离子浓度、催化剂、溶剂组成、离子强度、Mn2+、Al3+、温度等因素对反应动力学的影响。我们的研究表明,该反应对氧化剂和催化剂具有一级依赖性。反应对底物和H+的反应遵循分数级动力学。离子强度的增加对反应速率没有影响,介质介电常数的降低使反应速率降低。硫酸锰浓度的增加减慢了反应速率,证实了双电子转移参与了反应机理。不存在自由基机制的可能性,丙烯腈的加入证实了这一点,对反应速率没有显著影响,表明自由基不参与反应。根据实验观察,推导出了反应机理和速率规律。氧化产物为环氧查尔酮,并用红外光谱对其进行了表征。
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