R. Naik, A. Srivastava, A. Verma, S. Yadav, Ruchi Singh, S. Prasad
{"title":"高碘酸离子在水介质中氧化三乙四胺六乙酸钴酸盐(II)配合物的动力学及机理","authors":"R. Naik, A. Srivastava, A. Verma, S. Yadav, Ruchi Singh, S. Prasad","doi":"10.1515/IRM.2007.6.3.185","DOIUrl":null,"url":null,"abstract":"The kinetics and mechanism of oxidation of [Co(II)TTHA]4- (where TTHA = Triehylenetetraaminehexaaceticacid) by periodate ion has been studied in aqueous acidic medium. The reaction has been investigated spectrophotometrically at λmn = 550 nm under pseudo first- order condition by taking large excess of oxidant, [IO4-] at pH = 4.0 + 0.02, 1 = 0.1 M (CH3COONa + Na NO3) and at three different temperatures viz 150 C, 200 C and 250 C. The electron transfer reaction between [Co(II)TTHA]4- and , [IO4-] obeys inner- sphere reaction pathway through the formation of long lived intermediate complex which eventually get converted into a corresponding [Co(III)TTHA]3- complex as final reaction product. The experimental observations have shown that the reaction exhibit first- order dependence in [Co(II)TTHA]4- . The variation of pseudo- first- order rate constant (Kabc) with [IO4-] keeping other reaction variables fixed at constant value is found to obey the following empirical equation. Kabc = a[IO4-]2/b + c[IO4-] This rate law is consistent with a three step mechanistic scheme. The values of (Kabc) are almost invariant with increasing pH and attributed due to the reaction of deprotonated form of [Co(II)TTHA]4- complex and [IO4-] in the whole pH region. Eyring’s equations has been used to calculate the activation parameters and found to be ∆H* = 16.63 KJ mole-1 ; ∆S* = -214.00 JK-1 mole-1. These values are consistent with three step mechanistic scheme as proposed.","PeriodicalId":8996,"journal":{"name":"BioInorganic Reaction Mechanisms","volume":"34 1","pages":"185 - 192"},"PeriodicalIF":0.0000,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Kinetics and Mechanism of Oxidation of Triethylenetetraaminehexaacetatocobaltate(II) Complex by Periodate Ion in AqueousMedium\",\"authors\":\"R. Naik, A. Srivastava, A. Verma, S. Yadav, Ruchi Singh, S. Prasad\",\"doi\":\"10.1515/IRM.2007.6.3.185\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The kinetics and mechanism of oxidation of [Co(II)TTHA]4- (where TTHA = Triehylenetetraaminehexaaceticacid) by periodate ion has been studied in aqueous acidic medium. The reaction has been investigated spectrophotometrically at λmn = 550 nm under pseudo first- order condition by taking large excess of oxidant, [IO4-] at pH = 4.0 + 0.02, 1 = 0.1 M (CH3COONa + Na NO3) and at three different temperatures viz 150 C, 200 C and 250 C. The electron transfer reaction between [Co(II)TTHA]4- and , [IO4-] obeys inner- sphere reaction pathway through the formation of long lived intermediate complex which eventually get converted into a corresponding [Co(III)TTHA]3- complex as final reaction product. The experimental observations have shown that the reaction exhibit first- order dependence in [Co(II)TTHA]4- . The variation of pseudo- first- order rate constant (Kabc) with [IO4-] keeping other reaction variables fixed at constant value is found to obey the following empirical equation. Kabc = a[IO4-]2/b + c[IO4-] This rate law is consistent with a three step mechanistic scheme. The values of (Kabc) are almost invariant with increasing pH and attributed due to the reaction of deprotonated form of [Co(II)TTHA]4- complex and [IO4-] in the whole pH region. Eyring’s equations has been used to calculate the activation parameters and found to be ∆H* = 16.63 KJ mole-1 ; ∆S* = -214.00 JK-1 mole-1. These values are consistent with three step mechanistic scheme as proposed.\",\"PeriodicalId\":8996,\"journal\":{\"name\":\"BioInorganic Reaction Mechanisms\",\"volume\":\"34 1\",\"pages\":\"185 - 192\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2007-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BioInorganic Reaction Mechanisms\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1515/IRM.2007.6.3.185\",\"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.2007.6.3.185","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The Kinetics and Mechanism of Oxidation of Triethylenetetraaminehexaacetatocobaltate(II) Complex by Periodate Ion in AqueousMedium
The kinetics and mechanism of oxidation of [Co(II)TTHA]4- (where TTHA = Triehylenetetraaminehexaaceticacid) by periodate ion has been studied in aqueous acidic medium. The reaction has been investigated spectrophotometrically at λmn = 550 nm under pseudo first- order condition by taking large excess of oxidant, [IO4-] at pH = 4.0 + 0.02, 1 = 0.1 M (CH3COONa + Na NO3) and at three different temperatures viz 150 C, 200 C and 250 C. The electron transfer reaction between [Co(II)TTHA]4- and , [IO4-] obeys inner- sphere reaction pathway through the formation of long lived intermediate complex which eventually get converted into a corresponding [Co(III)TTHA]3- complex as final reaction product. The experimental observations have shown that the reaction exhibit first- order dependence in [Co(II)TTHA]4- . The variation of pseudo- first- order rate constant (Kabc) with [IO4-] keeping other reaction variables fixed at constant value is found to obey the following empirical equation. Kabc = a[IO4-]2/b + c[IO4-] This rate law is consistent with a three step mechanistic scheme. The values of (Kabc) are almost invariant with increasing pH and attributed due to the reaction of deprotonated form of [Co(II)TTHA]4- complex and [IO4-] in the whole pH region. Eyring’s equations has been used to calculate the activation parameters and found to be ∆H* = 16.63 KJ mole-1 ; ∆S* = -214.00 JK-1 mole-1. These values are consistent with three step mechanistic scheme as proposed.