Observation of the onset of torsion-induced, mode-specific dissipative intramolecular vibrational redistribution (IVR).

Evidence is found showing that coupling with vibration-torsion ("vibtor") levels of both in-plane and out-of-plane vibrations is instrumental in causing dissipative intramolecular vibrational redistribution (IVR). Both zero-electron-kinetic-energy (ZEKE) spectroscopy and two-dimensional laser-induced fluorescence (2D-LIF) spectroscopy are employed to investigate a series of bands located ∼1200 cm−1 above the S1 ← S0 origin in p-fluorotoluene. Transitions in this wavenumber region have been the focus of a number of studies probing IVR. By recording both ZEKE and 2D-LIF spectra, a prepared S1 population is projected onto both the ground state cation and ground state neutral energy states, respectively, giving added confidence to the assignments. The spectral region under discussion is dominated by a pair of fundamental bands, but for the first time, we present explicit evidence that this is complicated by contributions from a number of overtones and combinations, including vibtor levels. We deduce that very different extents of coupling are present across a 60 cm−1 window of the spectrum, even though the density of states is similar; in particular, one of the fundamentals couples efficiently to the increasing bath of levels, while one does not. We explain this by the influence of serendipitous near-coincidences of same-symmetry levels. [ABSTRACT FROM AUTHOR]