Suppr超能文献

关于FeIII(edta)与过氧化氢反应的进一步机理信息:第二个反应步骤的观察及pH值的重要性

Further mechanistic information on the reaction between FeIII(edta) and hydrogen peroxide: observation of a second reaction step and importance of pH.

作者信息

Brausam Ariane, van Eldik Rudi

机构信息

Institute for Inorganic Chemistry, University of Erlangen-Nürnberg, Egerlandstr. 1, 91058 Erlangen, Germany.

出版信息

Inorg Chem. 2004 Aug 23;43(17):5351-9. doi: 10.1021/ic0497580.

Abstract

A detailed study of the effect of buffer, temperature, and pressure on the reaction of hydrogen peroxide with Fe(III)(edta)H(2)O was performed using stopped-flow techniques. The reaction was found to consist of two steps and resulted in the formation of the already characterized high-spin Fe(III) side-on bound peroxo complex. The second step of the reaction was found to be independent of the hydrogen peroxide concentration. Formation of the purple peroxo complex is only observable above pH 7.5. Both reaction steps are affected by specific and general acid-catalysis. Five different buffer systems were used to clarify the role of general acid-catalysis in these reactions. Both reaction steps reveal an element of reversibility, which disappears on decreasing the acid concentration. The positive volumes of activation for both the forward and reverse reactions of the first step suggest a dissociative interchange substitution process for the reversible end-on binding of hydrogen peroxide to Fe(III)(edta)H(2)O. The small negative volume of activation for the second reaction step suggests an associative interchange mechanism for the formation of the side-on bound peroxo complex that is accompanied by dissociation of one of the four carboxylates of edta. A detailed mechanism in agreement with all the reported kinetic data is presented.

摘要

使用停流技术对缓冲液、温度和压力对过氧化氢与[Fe(III)(edta)H₂O]⁻反应的影响进行了详细研究。发现该反应由两步组成,并生成了已表征的高自旋Fe(III)侧基结合过氧络合物。发现反应的第二步与过氧化氢浓度无关。紫色过氧络合物仅在pH 7.5以上才可观察到。两个反应步骤均受特定酸催化和一般酸催化的影响。使用了五种不同的缓冲系统来阐明一般酸催化在这些反应中的作用。两个反应步骤均显示出可逆性,在降低酸浓度时这种可逆性消失。第一步正向和逆向反应的正活化体积表明,过氧化氢与[Fe(III)(edta)H₂O]⁻的可逆端基结合存在解离交换取代过程。第二个反应步骤的小负活化体积表明,侧基结合过氧络合物的形成存在缔合交换机制,同时伴随着edta四个羧酸盐之一的解离。提出了一个与所有已报道动力学数据一致的详细机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验