Vibrational Energy Relaxation of Selectively Excited Aromatic Molecules in Solution: The Effect of a Methyl Rotor and Its Chemical Substitution

Abstract

Transient femtosecond IR-pump-UV-probe spectroscopy is employed to investigate the intramolecular vibrational energy redistribution (IVR) and the intermolecular vibrational energy transfer (VET) of benzene, toluene (CH 3 -C 6 H 5 ), and α,α,α,-trifluorotoluene (CF 3 -C 6 H 5 ) selectively excited in overtones or combination bands of C-H stretch vibrations in solution. Global IVR and VET rate coefficients are derived from the measured transient absorption profiles using a simple kinetic model. The study reveals the effect of a methyl rotor and the effect of methyl rotor fluorination on the mechanisms and time scales of IVR and VET in aromatic model systems. For the present case, it turned out that the methyl rotor in toluene is not simply an enhancer for IVR; however, its fluorination accelerates IVR significantly. These results suggest that the methyl rotor effect on an aromatic ring in solution is more subtle than expected from previous gas-phase studies. In particular, the corresponding relaxation rates in this case are not simply governed by the number of lowest order resonances, such as found for aliphatic molecules. Instead, in aromatic molecules also, the very large number of higher order anharmonic resonances may play a pronounced role. Because the IVR rates are not at all correlated with the total density of states, we conclude that intramolecular vibrational energy relaxation of a zeroth order C-H stretch overtone or combination vibration in these molecules is not in its statistical limit and that hierarchical IVR, such as known for isolated molecules, still survives to some extent in solution. Our results further suggest that VET rates are not always simply correlated with the lowest frequency modes of the molecules.