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首页> 外文期刊>Bulletin of the Korean Chemical Society >The Kinetics of Complexation of Manganese(¥±), Cobalt(¥±) and Nickel(¥±) Ions with Some Dicarboxylates in Aqueous Solution
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The Kinetics of Complexation of Manganese(¥±), Cobalt(¥±) and Nickel(¥±) Ions with Some Dicarboxylates in Aqueous Solution

机译:锰(¥±),钴(¥±)和镍(¥±)离子与某些二羧酸盐在水溶液中的络合动力学

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The pressure-jump relaxation method has been used to determine the rate constants for the formation and dissociation of maganese(ケ), cobalt(ケ), and nickel(ケ) with some dicarboxylates in aqueous solution at zero ionic strength. The carboxylate ligands used are 3-nitrophthalate, 4-nitrophthalate, and phenylmalonate. The activation parameters have alse been obtained from the temperature dependence of the rate constants. A dissociative interchange mechanism with a chelate ring closure step as rate determining is employed to interpret the kinetic data of manganese(ケ) and cobalt(ケ) complexes. The rates of formation of nickel(ケ) complexes are controlled by both the solvent exchange step and the chelate ring closure step.
机译:跳压松弛法已用于确定锰(zero),钴(ケ)和镍(ケ)与一些二羧酸盐在零离子强度下的水溶液中形成和离解的速率常数。使用的羧酸盐配体是3-硝基邻苯二甲酸酯,4-硝基邻苯二甲酸酯和苯丙二酸酯。活化参数也已经从速率常数的温度依赖性获得。采用螯合环封闭步骤作为速率确定的解离交换机制来解释锰(ケ)和钴(ケ)配合物的动力学数据。镍(α)配合物的形成速率由溶剂交换步骤和螯合环封闭步骤两者控制。

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