Effect of ligand protonation on the facilitated ion transfer reactions across oil water interfaces. V. Applications of forced hydrodynamic conditions

被引:10
|
作者
Vega Mercado, Franco [1 ]
Manuel Ovejero, Juan [1 ]
Ariel Fernandez, Ricardo [1 ]
Alberto Dassie, Sergio [1 ]
机构
[1] Univ Nacl Cordoba, Inst Invest Fisicoquim Cordoba INFIQC, Dept Fisicoquim, CONICET,Fac Ciencias Quim, X5000HUA,Ciudad Univ, RA-5000 Cordoba, Argentina
关键词
Facilitated proton transfer; Forced hydrodynamic conditions; Liquidlliquid interface; Water autoprotolysis; Quinidine; LIQUID-LIQUID INTERFACE; LIQUID/LIQUID INTERFACE; PARTITION DIAGRAMS; CYCLIC VOLTAMMETRY; TRANSFER KINETICS; DEGRADED PRODUCT; CHANNEL FLOW; MECHANISM; NITROBENZENE; MICROPIPETTE;
D O I
10.1016/j.jelechem.2015.08.001
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Hydrodynamic forced conditions applied to the aqueous or the organic phase during a potential sweep can be used to elucidate the mechanisms of ion transfer across liquid' liquid interfaces. The aim of this study is to confirm experimentally the previous proposed global mechanisms of facilitated proton transfer via water autoprotolysis and to extend them, controlling the mass transport. We show that proton transfer assisted by quinidine via water autoprotolysis is an interesting example, where the ion transfer reaction occurs with the formation of different products in each phase, i.e., protonated weak base in the organic phase and the hydroxide ion in the aqueous phase. Furthermore, one of the reactants (water) is always in excess with respect to the other one (neutral weak base). These features provide unique characteristics to facilitated proton transfer via water autoprotolysis to be explored by applying forced hydrodynamic conditions. (C) 2015 Elsevier B.V. All rights reserved.
引用
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页码:100 / 104
页数:5
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