TY - JOUR
T1 - Intermolecular Dynamics of Room-Temperature Ionic Liquids: Femtosecond Optical Kerr Effect Measurements on 1-Alkyl-3-methylimidazolium Bis((trifluoromethyl)sulfonyl)imides
T2 - Femtosecond optical Kerr effect measurements on 1-alkyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imides
AU - Dzyuba, Sergei V.
AU - Hyun, Byung-Ryool
AU - Bartsch, Richard
AU - Quitevis, Edward
PY - 2002/8/22
Y1 - 2002/8/22
N2 - Using optically heterodyne-detected Raman-induced Kerr effect spectroscopy (OHD-RIKES) with 40 fs laser pulses, the transient birefringence in the room-temperature ionic liquids (RTILs), 1-alkyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imides, [Cnmim]NTf2 with n = 2, 4, 5, 6, 8, 10 (C2, C4, C5, C6, C8, C10), has been studied at room temperature and ambient pressure. Near zero delay, the OHD-RIKES response is dominated by the instantaneous electronic response. The nuclear response appears as a shoulder on the electronic response. Between 0 and 1 ps, the nuclear response is dominated by the intermolecular vibrational (nondiffusive) response. For C4, C5, C6, and C8, the 1/e time of the pseudo-exponential tail of the intermolecular response decreases with viscosity, in accord with the hydrodynamic model for vibrational dephasing. Superimposed on the OHD-RIKES response for C4, C5, and C6 is a coherent oscillation with a frequency of ∼140 cm-1. The intermolecular vibrational spectra for these RTILs obtained from the reduced OHD-RIKES data by using a Fourier transform procedure extend from 0 to 200 cm-1 and are bimodal with a low-frequency component at ∼22 cm-1 and a high-frequency component at ∼84 cm-1. The relative contribution of the high-frequency component to the total band increases in going from C2 to C5 and remains constant for C5, C6, and C8. The behavior of the reduced spectral densities is consistent with increasing order in the liquid. It is proposed that the 140 cm-1 oscillation arises from collective motions of locally ordered domains in the liquid.
AB - Using optically heterodyne-detected Raman-induced Kerr effect spectroscopy (OHD-RIKES) with 40 fs laser pulses, the transient birefringence in the room-temperature ionic liquids (RTILs), 1-alkyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imides, [Cnmim]NTf2 with n = 2, 4, 5, 6, 8, 10 (C2, C4, C5, C6, C8, C10), has been studied at room temperature and ambient pressure. Near zero delay, the OHD-RIKES response is dominated by the instantaneous electronic response. The nuclear response appears as a shoulder on the electronic response. Between 0 and 1 ps, the nuclear response is dominated by the intermolecular vibrational (nondiffusive) response. For C4, C5, C6, and C8, the 1/e time of the pseudo-exponential tail of the intermolecular response decreases with viscosity, in accord with the hydrodynamic model for vibrational dephasing. Superimposed on the OHD-RIKES response for C4, C5, and C6 is a coherent oscillation with a frequency of ∼140 cm-1. The intermolecular vibrational spectra for these RTILs obtained from the reduced OHD-RIKES data by using a Fourier transform procedure extend from 0 to 200 cm-1 and are bimodal with a low-frequency component at ∼22 cm-1 and a high-frequency component at ∼84 cm-1. The relative contribution of the high-frequency component to the total band increases in going from C2 to C5 and remains constant for C5, C6, and C8. The behavior of the reduced spectral densities is consistent with increasing order in the liquid. It is proposed that the 140 cm-1 oscillation arises from collective motions of locally ordered domains in the liquid.
UR - http://www.scopus.com/inward/record.url?scp=0037158962&partnerID=8YFLogxK
U2 - 10.1021/jp0141575
DO - 10.1021/jp0141575
M3 - Article
VL - 106
SP - 7579
EP - 7585
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 33
ER -