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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Kinetics of the Reaction of Chromium(VI) with Tris(1,10-phenanthroline)iron(II) Ions in Acidic Solutions.Anion and Medium Effects: Perchlorate versus Triflate
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Kinetics of the Reaction of Chromium(VI) with Tris(1,10-phenanthroline)iron(II) Ions in Acidic Solutions.Anion and Medium Effects: Perchlorate versus Triflate

机译:铬(VI)与三(1,10-菲咯啉)铁(II)离子在酸性溶液中反应的动力学阴离子和介质作用:高氯酸根与三氟甲磺酸根

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摘要

Reinvestigation of the reaction between title reagents in aqueous acidic triflate and perchlorate media revealed an unusual difference: the reaction is strictly first-order with respect to the concentration of Fe(phen)_3~(2+) (phen = 1,10-phenanthroline) in the triflate medium but shows an additional,but we believe artifactual,higher-order term in the perchlorate medium.We postulate that the apparent orders with respect to [Fe(phen)_3~(2+)] in (H/Li)ClO_4 do not indicate the actual chemical mechanism but,in whole or in part,the orders,particularly the higher-order component,reflect an interaction specific to Fe(phen)_3~(2+) or Fe(phen)_3~(3+) and ClO_4~- in solution.Data in (H/Li)O_3SCF_3 solutions indicate that,in the absence of added Fe(phen)_3~(3+),the first of the three sequential electron-transfer steps is rate controlling.Reactions started in the presence of the product Fe(phen)_3~(3+) occur somewhat more slowly,suggesting the first electron transfer is reversible.This finding allows the relative rate constants for Cr(V) oxidation and reduction to be evaluated,with limited precision,by two methods of analysis.The dependences on [Cr(VI)] can be resolved into contributions from the species HCrO_4~- and Cr_2O_7~(2-),each of which in turn depends on [H~+].The reaction mechanism is discussed in light of the data obtained in the triflate medium.Further,the rate constants for certain steps can be considered in light of E~0 for the Cr(VI)/(V) couple.
机译:重新研究酸性三氟甲磺酸盐水溶液和高氯酸盐介质中标题试剂之间的反应发现了一个不同寻常的差异:就Fe(phen)_3〜(2+)的浓度而言,该反应严格是一阶的(phen = 1,10-菲咯啉)在三氟甲磺酸盐介质中显示,但在高氯酸盐介质中显示了一个附加的,但我们认为是虚假的高阶项。我们假设(H / Li)中与[Fe(phen)_3〜(2+)]有关的表观有序)ClO_4并不表示实际的化学机理,而是全部或部分地反映了Fe(phen)_3〜(2+)或Fe(phen)_3〜( (H / Li)O_3SCF_3溶液中的数据表明,在不添加Fe(phen)_3〜(3+)的情况下,三个连续电子转移步骤中的第一个是速率在产物Fe(phen)_3〜(3+)存在下开始的反应发生的速度要慢一些,这表明第一次电子转移是可逆的。通过两种分析方法降低了要评估的Cr(V)氧化和还原的相对速率常数,但精度有限。可以将对[Cr(VI)]的依赖性分解为HCrO_4〜-和Cr_2O_7〜物种的贡献。 (2-),每个反过来取决于[H〜+]。根据在三氟甲磺酸酯(triflate)介质中获得的数据讨论了反应机理。此外,根据E〜可以考虑某些步骤的速率常数。 Cr(VI)/(V)对为0。

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