碱性高锰酸盐对l -天冬酰胺氧化脱胺和脱羧动力学的机理研究

M. R. Kembhavi, A. L. Harihar, S. Nandibewoor
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引用次数: 2

摘要

摘要采用分光光度法研究了碱性高锰酸盐在离子强度为0.50 mol dm-3条件下l -天冬酰胺(L-Aspg)氧化脱胺和脱羧的动力学。该反应在[高锰酸盐离子]中表现为一级动力学,在[L-Aspg]和[碱]中表现为分数级依赖性。初始添加的醛、氨、锰等产物对反应速率无显著影响。离子强度的增加和介质介电常数的降低增加了速率。碱性介质中的氧化过程有两种途径:一种是依赖底物的途径,另一种是不依赖底物的途径。对机理中涉及的常数进行了计算。在观测到的速率常数和计算得到的速率常数之间有很好的一致性。计算了路径I和路径II相对于慢步的激活参数。
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Kinetics of Oxidative Deamination and Decarboxylation of L-Asparagine by Alkaline Permanganate: a Mechanistic Approach
Abstract The kinetics of oxidative deamination and decarboxylation of L-asparagine (L-Aspg) by aqueous alkaline permanganate at constant ionic strength of 0.50 mol dm-3 were studied spectrophotometrically. The reaction exhibits first-order kinetics in [permanganate ion] and fractional-order dependences in [L-Aspg] and [alkali]. Initially added products such as aldehyde, ammonia and manganate have no significant effect on the rate of reaction. An increase in ionic strength and a decrease in dielectric constant of the medium increase the rate. The oxidation process in alkaline medium has shown to proceed via two paths: One a substrate dependent path, the other a substrate independent path. The constants involved in the mechanism were evaluated. There is a good agreement between observed and calculated rate constants. The activation paramaters with respect to slow step of path I and path II were calculated.
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