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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 >7,7 ',8,8 '-Tetracyanoquinodimethane as a redox probe for studying cation transfer across the water/2-nitrophenyl octyl ether interface at three-phase junctions supported by carbon ink screen-printed electrodes
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7,7 ',8,8 '-Tetracyanoquinodimethane as a redox probe for studying cation transfer across the water/2-nitrophenyl octyl ether interface at three-phase junctions supported by carbon ink screen-printed electrodes

机译:7,7',8,8'-四氰基氨基二甲基甲烷作为氧化还原探针,用于研究碳油墨丝网印刷电极支撑的三相连接处水/ 2-硝基苯基辛基醚界面上的阳离子转移

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The transfer of alkylammonium cations across the water/2-nitrophenyl octyl ether (NPOE) interface was studied at the three-phase junctions supported by a carbon ink screen-printed electrode (SPE) using cyclic and square-wave voltammetry. A microliter droplet of NPOE containing 7,7',8,8'-tetracyanoquinodimethane (TCNQ) was immobilized on the surface of the SPE and was immersed in aqueous solutions containing various alkylammonium salts. A plot of the half-wave transfer potential versus the logarithm of the cation concentration exhibits a close to Nernst slope. Moreover, a plot of the half-wave transfer potentials against the formal transfer potentials of alkylammonium cations yielded a slope close to unity. All these experimental facts suggest that the reduction of TCNQ at the SPE/NPOE interface is accompanied by a simultaneous cation transfer across the NPOE/water interface to preserve the electroneutrality of the organic microdroplet, namely the overall process corresponds to a cation-coupled electron transfer reaction. Finally, this approach allowed measuring the formal transfer potential of highly lipophilic cation, such as bis(triphenylphosphoranylidene)ammonium.
机译:使用循环和方波伏安法研究了碳油墨丝网印刷电极(SPE)支持的三相结处烷基铵阳离子在水/ 2-硝基苯基辛基醚(NPOE)界面上的转移。将含有7,7',8,8'-四氰基喹二甲烷(TCNQ)的微升NPOE液滴固定在SPE的表面上,并将其浸入含有各种烷基铵盐的水溶液中。半波传输电势与阳离子浓度的对数的关系图显示出接近能斯特斜率。此外,对烷基铵阳离子的形式转移电势的半波转移电势的图产生接近于一的斜率。所有这些实验事实表明,在SPE / NPOE界面处TCNQ的减少伴随着同时穿过NPOE /水界面的阳离子转移,以保持有机微滴的电子中性,即整个过程对应于阳离子耦合电子转移反应。最后,这种方法可以测量高度亲脂性阳离子(例如双(三苯基磷酰亚烷基)铵)的形式转移势。

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