Clusters of Imidazolium-Based Ionic Liquid in Benzene Solutions

Abstract

Cluster formation of 1-dodecyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide (C(12)mim(+)TFSA(-)) in benzene solutions was investigated using small-angle neutron scattering (SANS), NMR, attenuated total reflectance infrared (ATR-IR), and large-angle X-ray scattering (LAXS) techniques. The SANS measurements revealed that C(12)mim(+)TFSA(-) is heterogeneously mixed with benzene in the narrow range of benzene mole fraction 0.9 ≤ x(C6D6) ≤ 0.995 with a maximum heterogeneity at x(C6D6) ≈ 0.99. The NMR results suggested that the imidazolium ring is sandwiched between benzene molecules through the cation-π interaction. Moreover, TFSA(-) probably interacts with the imidazolium ring even in the range of x(C6H6) ≥ 0.9. Thus, the imidazolium rings, benzene molecules, and TFSA(-) would form clusters in the C(12)mim(+)TFSA(-)-benzene solutions. The LAXS measurements showed that the distance between the imidazolium ring and benzene is ∼3.8 Å with that between the benzene molecules of ∼7.5 Å. On the basis of these results, we discussed a plausible reason for the liquid-liquid equilibrium of the C(12)mim(+)TFSA(-)-benzene system.