可可碱与高锰酸盐离子在酸性水溶液中的电子转移反应

F. Jones, I. Anweting, I. E. Okon
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引用次数: 1

摘要

采用分光光度法研究了可可碱(以下简称TB)与高锰酸盐离子在T = 24, [H+] = 3.2 × 10-1 mol dm-3, I = 1.0 mol dm-3 (Na2SO4)的准一级条件下的电子转移反应。化学计量学研究表明,1摩尔高锰酸盐离子能消耗2摩尔TB。[TB]和[MnO4-]的反应速率都是一级反应,总的反应速率是二级反应。在研究范围内,[H+]和离子强度分别提高了反应速率。Michaelis-Mentens分析显示没有中间复杂地层的证据。观察了添加阴离子和阳离子对反应速率的催化作用。反应符合率法如下所示:- d (MnO4 -) / dt = (a + b (H +)) (MnO4(结核病) -]                                                                                     一个= 0.041 dm3mol-1 s - 1和b = 0.028 dm3mol-1 s - 1。因此,该反应是通过外球途径发生的,并提出了合理的反应机理。
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Electron Transfer Reaction of Theobromine and Permanganate Ion in Aqueous Acidic Media
Electron transfer reaction of theobromine (hereafter referred to as TB) and permanganate ion has been studied using spectrophotometric technique under pseudo first-order conditions at T = 24, [H+] = 3.2 × 10–1 mol dm–3and I = 1.0 mol dm–3 (Na2SO4). Stoichiometric study depicted that two moles of TB were consumed by one mole of permanganate ion. The rate of the reaction is first order in both [TB] and [MnO4-] and second order overall. It was observed that, [H+] and ionic strength respectively enhanced the rate of the reaction in the range studied. Michaelis-Mentens analysis showed no evidence of intermediate complex formation. Added anions and cations were observed to catalyze the reaction rate. The reaction conforms to the rate law as shown below:     -d [MnO4-]/dt = (a+b [H+]) [TB] [MnO4-]                                                                                     where a = 0.041 dm3mol–1 s–1 and   b= 0.028 dm3mol–1 s–1. The reaction thus occurs by an outer-sphere pathway and plausible mechanism is proposed for the reaction.
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