Effects of Aromaticity in Cations and Their Functional Groups on the Low-Frequency Spectra and Physical Properties of...

We have critically investigated the low-frequency spectra of six ionic liquids (ILs) consisting of systematically different cations having benzyl moieties or comparable-sized saturated cyclohexylmethyl groups, by means of femtosecond Raman-induced Kerr effect spectroscopy (fs-RIKES). The target ionic liquids are bis(trifluoromethylsulfonyl)amide ([NTf2](-)) salts of the 1-benzyl-3-methylimidazolium ([BzMIm](+)), 1-benzyl-1-methylpyrrolidinium ([BzMPyrr](+)), 1-benzylpyridinium ([BzPy](+)), 1-cyclohexylmethyl-3-methylimidazolium ([CHxmMIm](+)), 1-cyclohexylmethyl-1-methylpyrrolidinium ([CHxmMPyrr](+)), and 1-cyclohexylmethylpyridinium ([CHxmPy](+)) cations. The primary purpose of this study is to clarify the effects of charged and neutral aromatic moieties on the low-frequency spectrum and bulk properties such as liquid density, surface tension, shear viscosity, glass transition temperature, and melting point. We found that ILs with benzyl groups have larger surface tensions than those with the same cation bearing the cyclohexylmethyl group. The trend in the glass transition temperatures, comparing ILs having the same side group, is pyridinium > imidazolium > pyrrolidinium. The effects of a single aromatic moiety on the shear viscosity are inconclusive, although the viscosities of the ILs with aromatic moieties on both the cation and the benzyl group, i.e., [BzMIm][NTf2] and [BzPy][NTf2], are substantially lower than those of the other ILs at room temperature, as a consequence of their higher fragilities. In the low-frequency Kerr spectra in the frequency range of approximately 0.1 to 200 cm(-1) measured by fs-RIKES, the ILs possessing two aromatic groups show the largest relative intensity of the nuclear response to the electronic response. Both the charged and neutral aromatic rings show signals due to the ring libration; the neutral one appears at a lower frequency than the charged one. The relationship between the first moment of the broad low-frequency spectrum band and the bulk parameter consisting of the square root of the surface tension divided by the liquid density is obeyed by the cyclohexylmethyl derivatives whether the cation is aromatic or not, but not by the ILs with the neutral aromatic benzyl group. Quantum chemistry calculations have been also performed to understand the vibrational modes of the ionic species in the ILs.