Hammond Chris J, Ayles Victoria L, Bergeron Denis E, Reid Katharine L, Wright Timothy G
School of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
J Chem Phys. 2006 Sep 28;125(12):124308. doi: 10.1063/1.2354501.
We employ zero-kinetic-energy (ZEKE) photoelectron spectroscopy with nanosecond laser pulses to study intramolecular vibrational redistribution (IVR) in S(1) para-fluorotoluene. The frequency resolution of the probe step is superior to that obtained in any studies on this molecule to date. We focus on the behavior of the 13(1) (C-CH(3) stretch) and 7a(1) (C-F stretch) vibrational states whose dynamics have previously received significant attention, but with contradictory results. We show conclusively that, under our experimental conditions, the 7a(1) vibrational state undergoes significantly more efficient IVR than does the 13(1) state. Indeed, under the experimental conditions used here, the 13(1) state undergoes very little IVR. These two states are especially interesting because their energies are only 36 cm(-1) apart, and the two vibrational modes have the same symmetry. We discuss the role of experimental conditions in observations of IVR in some detail, and thereby suggest explanations for the discrepancies reported to date.
