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• W2060283485 abstract "The voltammetry of 7,7,8,8-tetracyanoquinodimethane (TCNQ) at an electrode-microparticle-aqueous (electrolye) interface has been proposed as a cation sensor on the basis that changes in electrolyte cation (analyte) concentrations result in reproducible shifts in the TCNQ0/- reversible potential. In order to probe the ion selective nature of the TCNQ sensor, the voltammetric response towards a series of tetraalkylammonium cations of variable size and hydrophobicity were studied. Both the thermodynamics (reversible potential) and kinetics (voltammetric peak separation) of the TCNQ0/- system were strongly dependant on the identity of the R4N+ cation. The reversible potential responded in a Nernstian manner to changes in cation concentration. When presented with mixed-analyte solutions, the TCNQ system exhibited Nicolsky type (or competitive) form of selectivity. However, the selectivity coefficients found in the present study were far greater than previously reported with group I cations. The order obtained for the tetraalkylammonium series indicates that ion selectivity is predominantly based on analyte solvation thermodyanics rather than a specific ionophore mechanism." @default.
• W2060283485 created "2016-06-24" @default.
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• W2060283485 date "2003-01-01" @default.
• W2060283485 modified "2023-10-13" @default.
• W2060283485 title "Ion selectivity obtained under voltammetric conditions when a TCNQ chemically modified electrode is presented with aqueous solutions containing tetraalkylammonium cations" @default.
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• W2060283485 doi "https://doi.org/10.1039/b309078g" @default.
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