Intramolecular energy transfer in highly vibrationally excited methanol. III. Rotational and torsional analysis

We report here torsional analysis of rotationally resolved spectra of the 3 nu(1), 5 nu(1), and 6 nu(1) (OH stretch) bands of jet-cooled methanol. The upper states are reached by a double resonance excitation scheme involving the selection of single rotational states in the n1 fundamental band. Detection of the overtone transitions (n nu(1)<--nu(1)) is by infrared laser assisted photofragment spectroscopy (IRLAPS). The torsional tunneling frequency declines monotonically from 9.1 cm(-1) in the vibrational ground state to 1.6 cm(-1) at 6 nu(1). For the available rotational levels at 3 nu(1) (K = 0-3) and 6 nu(1) (K = 0,1), the pattern of torsional energies is approximately regular. To obtain the vibrational dependence of the torsional barrier V-3, it was necessary to use the OH radical and HOOH as models for the vibrational dependence of the torsional inertial constant F. The assumed linear dependence of V-3 on nu(1) accounts for the torsional tunneling splittings at nu(1) = 0, 3, and 6 and for the pattern of the torsional energies. V-3 increases by 40-45 cm(-1) per quantum of OH excitation. (C) 1999 American Institute of Physics. [S0021-9606(99)02417-4].

Published in:
JOURNAL OF CHEMICAL PHYSICS, 110, 23, 11359-11367

 Record created 2005-12-15, last modified 2018-03-17

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