胶束介质中Mn(III)醋酸盐诱导α-氨基酸五胺钴(III)配合物的电子转移

S. Udhayavani, K. Subramani
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引用次数: 0

摘要

α-氨基酸的五胺钴(III)配合物在酸性介质中被醋酸锰(III)胶束催化氧化,最终产物为近100%的Co(II)和约100%的羰基化合物。在胶束存在的情况下,未结合的氨基酸产生约100%的羰基化合物。研究了硫酸浓度变化的影响。Co(III)配合物在λ=502 nm处的紫外可见吸光度下降接近初始吸光度的100%。尽管Mn(III)与未结合配体的化学计量为2:1,但Mn(III)与钴(III)配合物的比例为1:1,在钴(III)中心还原约为100%。计算了动力学和化学计量学的结果。提出了一种与实验结果一致的合适的机制,即加入一个自由基阳离子中间体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mn(III)acetate-Induced Electron Transfer in Pentaammine Cobalt(III)Complexes of α-Amino Acids in Micellar Medium
A micellar catalyzed oxidation of pentaamminecobalt(III) complexes of α-amino acids by Mn(III)acetate in acidic medium yielding nearly 100% Co(II) and about 100% carbonyl compounds are ultimate products. The unbound amino acids yield about 100% of carbonyl compound in presence of micelles. The effect of variation of sulphuric acid has been carried. The decrease in UV-Visible absorbance at λ=502 nm for Co(III) complex corresponds to nearly 100% of the initial absorbance. In spite of the stoichiometry of Mn(III) to unbound ligand is 2:1, the ratio of Mn(III) to cobalt(III) complex is 1:1 accounting for about 100% reduction at the cobalt(III) centre. The kinetic and stoichiometric results have been accounted. A suitable mechanism consistent with the experimental findings has been proposed by involving a radical cation intermediate.
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来源期刊
E-journal of Chemistry
E-journal of Chemistry CHEMISTRY, MULTIDISCIPLINARY-
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