首页> 外文期刊>International Journal of Advanced Chemistry >Electron transfer reaction of Tris(1,10-phenanthroline) cobalt(III) complex [Co(phen)3]3+ and thiosulphate ion (S2O32?) in an aqueous acidic medium
【24h】

Electron transfer reaction of Tris(1,10-phenanthroline) cobalt(III) complex [Co(phen)3]3+ and thiosulphate ion (S2O32?) in an aqueous acidic medium

机译:三(1,10-菲咯啉)钴(III)配合物[Co(phen)3] 3+与硫代硫酸根离子(S2O32?)的电子转移反应

获取原文
           

摘要

The electron transfer reaction of Tris (1,10-phenanthroline)cobalt(III) complex by thiosulphate ion has been studied in an aqueous acidic medium. Stoichiometric determination shows that for one mole of the oxidant that was reduced, one mole of the reductant was consumed; the reaction conforms to an overall equation: 2[Co(phen) 3 ] 3+ + 2S 2 O 3 2? → 2[Co(phen) 3 ] 2+ + S 4 O 6 2? Kinetics study carried out under pseudo-first order condition shows that the reaction proceeded via a one-way acid-dependent pathway and was third order overall; zero order with respect to the oxidant concentration, second order with respect to the reductant concentration and first order with respect to the hydrogen ion concentration. The empirical rate law conforms to the equation: ? {Co(phen) 3 } 3+ ] = a [H + ] [S 2 O 3 2? ] 2 ‘a’ = 128.26 dm 6 mol ?2 s ?1 : at [H + ] = 2.0 × 10 ?2 mol dm ?3 , μ = 0.4 mol dm ?3 (NaCl), T = 28 ± 1?C and λ max = 495 nm. The rate of reaction increased at the increase in ionic strength and at the decrease in medium dielectric constant. Added cations and anions catalyzed and inhibited the reaction rates respectively. The Michaelis-Menten plot of 1/k 1 versus 1/[S 2 O 3 2? ] 2 started from the origin. Hence based on spectroscopic investigation, thermodynamic information from temperature dependence studies and kinetic evidence from Michaelis–Menten plots and the interactions with added ions, an outer-sphere mechanism has been rationalized for this reaction. The mechanistic scheme of the reaction was proposed via the stated mechanistic route.
机译:已经研究了在酸性水溶液中硫代硫酸根离子对三(1,10-菲咯啉)钴(III)配合物的电子转移反应。化学计量确定表明,还原的一摩尔氧化剂消耗掉一摩尔的还原剂;反应符合一个整体方程:2 [Co(phen)3] 3+ + 2S 2 O 3 2? →2 [Co(phen)3] 2+ + S 4 O 6 2?在拟一级反应条件下进行的动力学研究表明,反应是通过单向酸依赖性途径进行的,总体上是三级反应。氧化剂浓度为零级,还原剂浓度为二级,氢离子浓度为一级。经验率定律符合以下方程式: {Co(phen)3} 3+] = a [H +] [S 2 O 3 2? ] 2'a'= 128.26 dm 6 mol?2 s?1:[H +] = 2.0×10?2 mol dm?3,μ= 0.4 mol dm?3(NaCl),T = 28±1°C λmax = 495 nm。反应速率随着离子强度的增加和介质介电常数的减小而增加。添加的阳离子和阴离子分别催化和抑制了反应速率。 1 / k 1对1 / [S 2 O 3 2?的Michaelis-Menten图。 ] 2从原点开始。因此,基于光谱学研究,温度依赖性研究的热力学信息以及Michaelis-Menten图的动力学证据以及与添加离子的相互作用,已为该反应合理化了外层机理。通过所述机理路线提出了反应的机理方案。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号