首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Voltammetric study of the interfacial electron transfer between bis(butylcyclopentadienyl)iron in 1,2-dichloroethane and hexacyanoferrate in water
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Voltammetric study of the interfacial electron transfer between bis(butylcyclopentadienyl)iron in 1,2-dichloroethane and hexacyanoferrate in water

机译:伏安法研究1,2-二氯乙烷中双(丁基环戊二烯基)铁与水中六氰合铁酸盐之间的界面电子转移

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摘要

The electron transfer (ET) reaction between bis(butylcyclopentadienyl)iron(II) ([Fe-II(C5H4Bu)(2)]) in 1,2-dichloroethane (1,2-DCE) and the hexacyanoferrate redox couple ([Fe-II/III(CN)(6)](4-/3-)) in water (W) at the 1,2-DCE vertical bar W interface has been studied by use of normal pulse voltammetry and cyclic voltammetry. In normal pulse voltammetry, S-shaped current vs. potential curves with well-defined limiting currents attributable to the interfacial ET reaction were observed. The voltammetric results can be explained well by the theoretical equations [M. Senda, Rev. Polarogr. (Jpn), 49 (2003) 219; 50 (2004) 60] according to a so-called IT-mechanism, that is, the [Fe-II(C5H4Bu)(2)] Molecule is transferred from the 1,2-DCE to the W phase across the interface, then the ET reaction takes place homogeneously in the W phase between [Fe-III(CN)(6)](3-)(W) and [Fe-II(C5H4Bu)(2)](W) to produce [Fe-II(CN)(6)](4-)(W) and [Fe-III(C5H4Bu)(2)](+)(W), which is followed by the transfer of the [Fe-III(C5H4Bu)(2)](+) ion from the W to the 1,2-DCE phase across the interface to give the voltammetric current. Experimental results from cyclic voltammetry are also explained well by the IT-mechanism. (c) 2004 Elsevier B.V. All rights reserved.
机译:双(丁基环戊二烯基)铁(II)([Fe-II(C5H4Bu)(2)])在1,2-二氯乙烷(1,2-DCE)中与六氰合铁酸盐氧化还原对([Fe通过使用常规脉冲伏安法和循环伏安法研究了1,2-DCE垂直条形W界面在水(W)中的-II / III(CN)(6)](4- / 3-))。在常规脉冲伏安法中,观察到S型电流与电位曲线的关系,该曲线具有明确定义的归因于界面ET反应的极限电流。伏安法的结果可以用理论方程[M。 Senda,Rev。Polarogr。 (Jpn),49(2003)219; 50(2004)60]根据所谓的IT机制,即[Fe-II(C5H4Bu)(2)]分子通过界面从1,2-DCE转移到W相,然后ET反应在[Fe-III(CN)(6)](3-)(W)和[Fe-II(C5H4Bu)(2)](W)之间的W相中均匀发生(CN)(6)](4-)(W)和[Fe-III(C5H4Bu)(2)](+)(W),然后转移[Fe-III(C5H4Bu)(2 )](+)离子从W到界面上的1,2-DCE相产生伏安电流。 IT机理也很好地解释了循环伏安法的实验结果。 (c)2004 Elsevier B.V.保留所有权利。

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