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首页> 外文期刊>Zeitschrift fur Physikalische Chemie: International Journal of Research in Physical Chemistry and Chemical Physics >Spectrophotometric Studies of Reactions of the Aquapentacyanoferrate(II) Ion with Ketones.Kinetics and Mechanism of the Substitution Reaction of the Aquapentacyanoferrate(II) Ion with 1-Benzoylethylpyridinium Chloride
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Spectrophotometric Studies of Reactions of the Aquapentacyanoferrate(II) Ion with Ketones.Kinetics and Mechanism of the Substitution Reaction of the Aquapentacyanoferrate(II) Ion with 1-Benzoylethylpyridinium Chloride

机译:水合五氰基高铁酸酯(II)离子与酮反应的分光光度研究。水合五氰基高铁酸酯(II)离子与1-苯甲酰基乙基吡啶鎓氯化物取代的动力学和机理

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摘要

The carbonyl group of compounds of the phenacyl- and benzoylethyl-pyridinium type is recognized as a potential a donor ligand which can produce complexes with the aquapentacyanoferrate(II) ion.Its reactive form is the ionized one i.e.the enolate ion.A detailed Spectrophotometric investigation has been made for the reaction of the aquapentacyanoferrate(II) ion with 1-benzoylethylpyridinium chloride.The equilibrium constant of the produced complex was derived using two literatury available additional types of processing the molar ratio method's experimental data which were not found to be applied to this type of complexes.The kinetics of this substitution reaction were studied in buffered solutions at pH = 8.0 and / = 0.05M.The obtained results are consistent with a dissociative mechanism.
机译:苯甲酰基-和苯甲酰基乙基-吡啶鎓类型的化合物的羰基被认为是潜在的供体配体,可以与水合戊酸高铁酸根离子(II)生成络合物,其反应形式是被离子化的一种,即烯醇酸根离子。季戊四酸高铁酸根离子(II)与1-苯甲酰基乙基吡啶鎓氯化物的反应已被制备。使用两种可用的其他文学类型的摩尔比方法的实验数据来处理制得的配合物的平衡常数。在pH = 8.0和/ = 0.05M的缓冲溶液中研究了这种取代反应的动力学。所得结果与解离机理相符。

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