过硫酸盐-铁(II)和镍(II)-肟-亚胺配合物之间的电子转移反应动力学研究

B. Saha, M. Ali, S. Gangopadhyay, Nizamuddin Shaikh, P. Banerjee
{"title":"过硫酸盐-铁(II)和镍(II)-肟-亚胺配合物之间的电子转移反应动力学研究","authors":"B. Saha, M. Ali, S. Gangopadhyay, Nizamuddin Shaikh, P. Banerjee","doi":"10.1080/10286620210353","DOIUrl":null,"url":null,"abstract":"The kinetics of the oxidation of complexes, [Fe(H 2 L) 2+ and [Ni(HL')] 2+ (H 2 L u = u 3,14-dimethyl-4,7,10,13-tetraazadeca-3,13-diene-2,5-dione-dioxime, (I)) and HL'=15-amino-3-methyl-4,7,10,13-tetraazapentadec-3-ene-2-one-oxime, (II)) by peroxodisulfate ion was studied spectrophotometrically under pseudo-first-order conditions keeping the complexes as minor components, within the pH range 3.0-7.93 at I =0.20 u mol u dm m 3 (NaClO 4 ) for the former and I =0.25 u mol u dm m 3 for the latter complex at 303 u K. At a particular pH, plots of k obs vs. [S 2 O 8 2 m ] yield ascending curves with decreasing slope values for both the reactions, and the general rate law: d/d t [complex]=2 kQ [S 2 O 8 2 m ]/(1+ Q [S 2 O 8 2 m ]) is followed. A pre-equilibrium ion-pair formation between the reactants prior to electron transfer is proposed. A plot of m [log( k 12 / W 12 ) m 1/2 u log u k 22 ] vs. 1/2 u log( K 12 f 12 ) for such reactions yields a straight line with slope m (0.73 - 0.10) which deviates significantl...","PeriodicalId":54977,"journal":{"name":"Inorganic Reaction Mechanisms","volume":"3 1","pages":"173-180"},"PeriodicalIF":0.0000,"publicationDate":"2002-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Electron Transfer Reactions Between Peroxodisulfate-and Iron(II) and Nickel(II)-oxime-imine Complexes--a Kinetic Study\",\"authors\":\"B. Saha, M. Ali, S. Gangopadhyay, Nizamuddin Shaikh, P. Banerjee\",\"doi\":\"10.1080/10286620210353\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The kinetics of the oxidation of complexes, [Fe(H 2 L) 2+ and [Ni(HL')] 2+ (H 2 L u = u 3,14-dimethyl-4,7,10,13-tetraazadeca-3,13-diene-2,5-dione-dioxime, (I)) and HL'=15-amino-3-methyl-4,7,10,13-tetraazapentadec-3-ene-2-one-oxime, (II)) by peroxodisulfate ion was studied spectrophotometrically under pseudo-first-order conditions keeping the complexes as minor components, within the pH range 3.0-7.93 at I =0.20 u mol u dm m 3 (NaClO 4 ) for the former and I =0.25 u mol u dm m 3 for the latter complex at 303 u K. At a particular pH, plots of k obs vs. [S 2 O 8 2 m ] yield ascending curves with decreasing slope values for both the reactions, and the general rate law: d/d t [complex]=2 kQ [S 2 O 8 2 m ]/(1+ Q [S 2 O 8 2 m ]) is followed. A pre-equilibrium ion-pair formation between the reactants prior to electron transfer is proposed. A plot of m [log( k 12 / W 12 ) m 1/2 u log u k 22 ] vs. 1/2 u log( K 12 f 12 ) for such reactions yields a straight line with slope m (0.73 - 0.10) which deviates significantl...\",\"PeriodicalId\":54977,\"journal\":{\"name\":\"Inorganic Reaction Mechanisms\",\"volume\":\"3 1\",\"pages\":\"173-180\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Reaction Mechanisms\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/10286620210353\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Reaction Mechanisms","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/10286620210353","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

在伪一阶条件下,以小组分的形式研究了配合物[Fe(h2 L) 2+和[Ni(HL')] 2+ (h2 L u = 3,14-二甲基-4,7,10,13-四氮杂碳-3,13-二烯-2,5-二酮-二肟,(I))和HL'=15-氨基-3-甲基-4,7,10,13-四氮杂碳-3-烯-2-一肟,(II))被过氧化物二磺酸离子氧化的动力学。pH值范围内3.0 - -7.93 = 0.20 u摩尔dm我3 (NaClO 4)前我= 0.25 u摩尔dm 3后者复杂303 u k . pH值在一个特定的块奥林匹克广播服务公司与k [S 2 O 8 2 m]收益率上升与下降斜率值的反应曲线,和一般速率定律:d / d t(复杂的)= 2 kQ [S 2 O 8 2 m] / (1 + Q [S 2 O 8 2 m])之后。在电子转移之前,反应物之间形成了一个预平衡离子对。这类反应的m [log(k 12 / W 12) m 1/2 u log u k 22]与1/2 u log(k 12 f 12)的曲线得到斜率为m(0.73 - 0.10)的直线。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electron Transfer Reactions Between Peroxodisulfate-and Iron(II) and Nickel(II)-oxime-imine Complexes--a Kinetic Study
The kinetics of the oxidation of complexes, [Fe(H 2 L) 2+ and [Ni(HL')] 2+ (H 2 L u = u 3,14-dimethyl-4,7,10,13-tetraazadeca-3,13-diene-2,5-dione-dioxime, (I)) and HL'=15-amino-3-methyl-4,7,10,13-tetraazapentadec-3-ene-2-one-oxime, (II)) by peroxodisulfate ion was studied spectrophotometrically under pseudo-first-order conditions keeping the complexes as minor components, within the pH range 3.0-7.93 at I =0.20 u mol u dm m 3 (NaClO 4 ) for the former and I =0.25 u mol u dm m 3 for the latter complex at 303 u K. At a particular pH, plots of k obs vs. [S 2 O 8 2 m ] yield ascending curves with decreasing slope values for both the reactions, and the general rate law: d/d t [complex]=2 kQ [S 2 O 8 2 m ]/(1+ Q [S 2 O 8 2 m ]) is followed. A pre-equilibrium ion-pair formation between the reactants prior to electron transfer is proposed. A plot of m [log( k 12 / W 12 ) m 1/2 u log u k 22 ] vs. 1/2 u log( K 12 f 12 ) for such reactions yields a straight line with slope m (0.73 - 0.10) which deviates significantl...
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信