{"title":"碱性高锰酸盐自由基诱导l -胱氨酸氧化动力学研究","authors":"M. R. Kembhavi, R. G. Panari, S. Nandibewoor","doi":"10.1515/irm-1999-0306","DOIUrl":null,"url":null,"abstract":"Abstract The kinetics of oxidation of L-cystine by alkaline permanganate follows the rate law, where Κ is the formation constant for the complex between L-cystine and permanganate and k is the decomposition rate constant. The data suggest that the oxidation of L-cystine proceeds via the formation of a complex between L-cystine and permanganate which decomposes slowly, followed by a fast reaction between the free radical of L-cystine and another molecule of permanganate to give the products. The reaction constants involved in the mechanism are derived. There is good agreement between the observed and calculated rate constants under varying experimental conditions. The activation parameters are computed with respect to the slow step of the mechanism.","PeriodicalId":8996,"journal":{"name":"BioInorganic Reaction Mechanisms","volume":"42 1","pages":"225 - 232"},"PeriodicalIF":0.0000,"publicationDate":"1999-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Free Radical Induced Oxidation of L-Cystine by Alkaline Permanganate - A Kinetic Study\",\"authors\":\"M. R. Kembhavi, R. G. Panari, S. Nandibewoor\",\"doi\":\"10.1515/irm-1999-0306\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract The kinetics of oxidation of L-cystine by alkaline permanganate follows the rate law, where Κ is the formation constant for the complex between L-cystine and permanganate and k is the decomposition rate constant. The data suggest that the oxidation of L-cystine proceeds via the formation of a complex between L-cystine and permanganate which decomposes slowly, followed by a fast reaction between the free radical of L-cystine and another molecule of permanganate to give the products. The reaction constants involved in the mechanism are derived. There is good agreement between the observed and calculated rate constants under varying experimental conditions. The activation parameters are computed with respect to the slow step of the mechanism.\",\"PeriodicalId\":8996,\"journal\":{\"name\":\"BioInorganic Reaction Mechanisms\",\"volume\":\"42 1\",\"pages\":\"225 - 232\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1999-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BioInorganic Reaction Mechanisms\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1515/irm-1999-0306\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BioInorganic Reaction Mechanisms","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/irm-1999-0306","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
摘要
l -胱氨酸被碱性高锰酸盐氧化的动力学遵循速率定律,其中Κ为l -胱氨酸与高锰酸盐络合物的形成常数,k为分解速率常数。数据表明,l -胱氨酸的氧化是通过l -胱氨酸和高锰酸盐之间形成络合物进行的,该络合物缓慢分解,然后l -胱氨酸自由基与另一分子高锰酸盐发生快速反应生成产物。导出了反应机理中涉及的反应常数。在不同的实验条件下,速率常数的观测值与计算值吻合较好。根据机构的慢步,计算了激活参数。
Free Radical Induced Oxidation of L-Cystine by Alkaline Permanganate - A Kinetic Study
Abstract The kinetics of oxidation of L-cystine by alkaline permanganate follows the rate law, where Κ is the formation constant for the complex between L-cystine and permanganate and k is the decomposition rate constant. The data suggest that the oxidation of L-cystine proceeds via the formation of a complex between L-cystine and permanganate which decomposes slowly, followed by a fast reaction between the free radical of L-cystine and another molecule of permanganate to give the products. The reaction constants involved in the mechanism are derived. There is good agreement between the observed and calculated rate constants under varying experimental conditions. The activation parameters are computed with respect to the slow step of the mechanism.