Ion-transfer voltammetry at 1,6-dichlorohexane|water and 1,4-dichlorobutane|water interfaces

Abstract

The usefulness of 1,6-dichlorohexane (1,6-DCH) and 1,4-dichlorobutane (1,4-DCB) as organic solvent (O) for ion-transfer voltammetry at O|water (W) interface has been examined, and the results are compared with those with 1,2-dichloroethane (1,2-DCE). The width of potential window of the 0.1 M tetraoctylammonium tetrakis(4-chlorophenyl)borate (O)|0.05 M Li 2SO 4 (W) interface increased in the sequence: O = 1,6-DCH > 1,4-DCB > 1,2-DCE. The voltammetric behavior of the transfer of various cations and anions at the 1,6-DCH|W and 1,4-DCB|W interfaces has been shown to be of reversible nature, and the midpoint potentials or the reversible half-wave potentials have been determined. The midpoint potentials of hydrophilic ions have also been determined by the analysis of anodic final rise or cathodic final decent of the voltammograms with the O|W interfaces, where the W contains a salt of the hydrophilic ion. Also, the effect of ion-pair formation in O on the midpoint potentials has also been discussed.