Investigation of liquid-liquid interfacial electron transfer kinetics using multicenter ferrocenyl complexes

被引:5
|
作者
Xiang, Debo [1 ,2 ]
Merbouh, Nabyl [1 ]
Shao, Huibo [2 ]
Yu, Hua-Zhong [1 ]
机构
[1] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
[2] Beijing Inst Technol, Dept Chem, Fac Sci, Beijing 100081, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
Multi-center ferrocenyl complex; Electron transfer rates; Liquid/liquid interface; Thin-layer electrochemistry; Thermodynamic driving force; LINKED CYCLOPENTADIENIDE IONS; THIN-LAYER ELECTROCHEMISTRY; LIQUID/LIQUID INTERFACES; POTENTIAL DEPENDENCE; GRAPHITE-ELECTRODES; CHARGE-TRANSFER; DRIVING-FORCE; FREE-ENERGY; RATES; DERIVATIVES;
D O I
10.1016/j.electacta.2011.04.062
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The redox behavior of two novel multicenter redox molecules (triferrocenylmethane and triferrocenyl-methanol) has been studied in a thin film of nitrobenzene (NB) imposed between a graphite electrode and an aqueous electrolyte. The well separated three sets of redox peaks indicate strong intramolecular electronic communications between the three ferrocene centers in each molecule. They were adapted as model compounds for the study of electron transfer kinetics across the liquid/liquid interface with varied overall driving force using only one-type redox couples in the organic and aqueous phase, respectively. It has been shown that in both cases the dependence of interfacial electron transfer rate on the increased overall driving force across the nitrobenzene/water interface is not monotonic. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5788 / 5793
页数:6
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