Orientational Time Correlation Functions for Vibrational Sum-Frequency Generation. 3. Methanol

Molecular dynamics simillaions have been used to study the orientational dynamics of methanol at the liquid/vapor and liquid/silica interfaces Orientational time correlation functions for the symmetric and asymmetric methyl stretches of methanol have been calculated to assess the role ofreorientationtn the vibrational Sum-frequency generation (VSFG), spectroscopy of these modes at the two interfaces. We find that internal methyl rotation plays significant pale in suppressing the intensity of the asymmetric methyl stretches at the liquid/Vapor interface. The broad orientational distribution of the methyl groups and the properties of the Raman Spectra of the asymmetric stretches are also major contributors to the low intensity of these modes in VSFG spectra at this interface. We find that after an initial rapid, inertial decay, there is little coupling among the orientational degrees of freedom of the methyl group, which suggests that time dependent VSFG spectroscopy may be used to probe interfacial Orientational dynamics in this and other hydrogen-bonded liquids.