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Spectroelectrochemical approaches to heterogeneous electron transfer reactions at the polarised water|1,2-dichloroethane interfaces

机译:极化水| 1,2-二氯乙烷界面上非均相电子转移反应的光谱电化学方法

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摘要

Heterogeneous electron transfer (ET) reactions at the polarised water|1,2-dichloroethane (DCE) interface are studied by in situ UV-Visible spectroscopy in total internal reflection mode. The reduction of 7,7,8,8-tetracyanoquinodimethane (TCNQ) and the oxidation of 1,1'-dimethylferrocene (DMFc) by the hexacyanoferrate redox couple are considered. The generation of products in the organic phase is monitored spectroscopically and correlated to the simultaneous current response. Both systems exhibit a good correlation between optical and electrochemical responses, highlighting the ideal behaviour of these redox couples for electron transfer studies at liquid|liquid interfaces.The kinetics of ET between hexacyanoferrate and TCNQ is analysed also by chronoabsorptometry and potential modulated reflectance spectroscopy. The potential dependence of the ET rate constant is discussed within the framework of the ET models for ITIES.
机译:通过全内反射模式下的原位紫外-可见光谱研究了极化的1,2 |-二氯乙烷(DCE)界面上的异质电子转移(ET)反应。考虑到7,7,8,8-四氰基喹二甲烷(TCNQ)的还原和六氰合铁酸酯氧化还原对对1,1'-二甲基二茂铁(DMFc)的氧化。用光谱法监测有机相中产物的产生并将其与同时的电流响应相关联。两种体系在光学和电化学响应之间均显示出良好的相关性,突显了这些氧化还原对在液-液界面进行电子转移研究的理想行为。六氰合铁酸盐和TCNQ之间的ET动力学还通过计时吸收法和电势调制反射光谱法进行了分析。在ET的ET模型框架内讨论了ET速率常数的潜在依赖性。

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