Ionic liquids composed of a hydrophobic anion, tetrakis[3,5-bis(trifluoromethyl)phenyl]borate (TFPB-), and various aromatic and aliphatic ammonium have been prepared. TFPB salts of N-octadecylisoquinolinium (C18Iq+) and trioctylmethylammonium (TOMA+) show low melting points of 31 and 36 degrees C, respectively, whereas TFPB-based ionic liquids of 1-alkyl-3-methylimidazolium with the alkyl chain length of 5-12 show melting points lower than 90 degrees C. The [C(18)Iq][TFPB]|water (W) and [TOMA][TFPB]|W interfaces have the polarized potential window (ppw) of 0.8 V at 56 degrees C, which is twice as wide as the ppw at the interface between W and room-temperature ionic liquids of bis(perfluoroalkylsulfonyl)imide so far reported. The extension of the ppw by more than 0.4 V to the positive direction enables voltammetric measurements of the ion transfer of relatively hydrophobic anions such as bis(trifluoromethylsulfonyl)imide and bis(pentafluoroethylsulfonyl)imide and of hydrophilic cations such as tetraethylammonium and acetylcholine ions.

The facilitated transfer of alkali metal cations (Li+, Na+, K+, Rb+, Cs+) by dibenzo-18-crown-6 (DB18C6) across the electrochemically polarizable interface between an aqueous solution (W) and a hydrophobic ionic liquid, N-octadecylisoquinolinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate ([C18Iq][TFPB]), has been studied using cyclic voltammetry at the interface formed at the tip of a micropipet. In cyclic voltammograms (CVs), the current due to the facilitated transfer of the cations by DB18C6 from W to [C18Iq][TFPB] can be measured within the polarized potential window of the [C(18)Iq][TFPB]|W interface. The stoichiometry of the complexes in [C18Iq][TFPB] for Li+, Na+, K+, and Rb+ are found to be 1:1 while for the Cs+ transfer both 1:1 and 1:2 complexes are likely to be formed. The formation constants of the 1:1 complexes for Li+, Na+, K+, and Rb+ in [C18Iq][TFPB], , evaluated from CVs are log = 5.0, 7.0, 8.2, and 7.3, respectively. The value for K+ is 1 order of magnitude greater than that for Na+. This higher selectivity of DB18C6 to K+ over Na+ in [C18Iq][TFPB] compared with that in molecular solvents suggests that the RTIL provides a unique solvation environment for the complexations of DB18C6 with the ions.

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Ion transfer across the polarized interface between a room-temperature ionic liquid (RTIL) or room-temperature molten salt, tetrahexylammonium bis(trifluoromethylsulfonyl)imide (THAC1C1N), and water has been studied voltammetrically using a micro liquid-liquid interface formed at the orifice of a glass capillary micropipette. A small current of nanoampere level circumvents the problem of the iR drop in the viscous ionic liquid phase. Voltammograms for the transfer of moderately hydrophilic ions, such as BF4 -and ClO4 -, from the aqueous phase in the capillary to the bulk of THAC1C1N in which the capillary is submerged, show steady-state characteristics in that the current does not depend on the scan rate up to a few hundred millivolt per second, and the plateau in the limiting current region is proportional to the bulk concentration of analyte ions. Owing to the steady-state current, which is presumably ascribed to a noncylindrical geometry of the capillary tip, the relative magnitude of the hydrophobicity, or the affnity to the RTIL, of a series of ions can be determined from the half-wave potentials of voltammograms.

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