首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Kinetics and mechanism of the reduction of pentacyanonitroferrate(III) by L-ascorbic acid in acidic aqueous solution
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Kinetics and mechanism of the reduction of pentacyanonitroferrate(III) by L-ascorbic acid in acidic aqueous solution

机译:L-抗坏血酸在酸性水溶液中还原五氰基硝酸铁(III)的动力学和机理

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摘要

The electron transfer reaction between [Fe(CN)(5)(NO2)](3-) and ascorbic acid was subjected to a detailed kinetic and thermodynamic study as a function of pH, ascorbic acid concentration, temperature and pressure. The pH profile indicates a pH independent region in the pH 5.0-5.5 range, which is ascribed to the oxidation of the ascorbate anion HA(-) present in solution under such conditions. The experimental rate and activation parameters suggest that this redox process follows an outer-sphere electron transfer mechanism. The Marcus, Fuoss and Stranks-Marcus-Hush relationships were applied to estimate the self-exchange rate constant for the [Fe(CN)(5)(NO2)](3-/4-) couple, the ion-pair formation constant, the rate constant for electron transfer and the value of Delta V(et)double dagger. The results are discussed in reference to related systems reported in the literature. [References: 35]
机译:[Fe(CN)(5)(NO2)](3-)与抗坏血酸之间的电子转移反应根据pH,抗坏血酸浓度,温度和压力进行了详细的动力学和热力学研究。 pH曲线表明在pH 5.0-5.5范围内的pH独立区域,这归因于在这种条件下溶液中存在的抗坏血酸阴离子HA(-)的氧化。实验速率和活化参数表明该氧化还原过程遵循外球电子转移机理。应用Marcus,Fuoss和Stranks-Marcus-Hush关系来估计[Fe(CN)(5)(NO2)](3- / 4-)对的自交换速率常数,离子对形成常数,电子传输的速率常数和Delta V(et)双匕首的值。参考文献中报道的相关系统讨论结果。 [参考:35]

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