Observation of b2_2 symmetry vibrational levels of the SO2_2 $\tilde{\mbox{C}}$ 1^1B2_2 state: Vibrational level staggering, Coriolis interactions, and rotation-vibration constants

preprint2016arXivOpen access

Abstract

The C~\mathrm{\tilde{C}} 1^1B2_2 state of SO2_2 has a double-minimum potential in the antisymmetric stretch coordinate, such that the minimum energy geometry has nonequivalent SO bond lengths. However, low-lying levels with odd quanta of antisymmetric stretch (b2_2 vibrational symmetry) have not previously been observed because transitions into these levels from the zero-point level of the X~\mathrm{\tilde{X}} state are vibronically forbidden. We use IR-UV double resonance to observe the b2_2 vibrational levels of the C~\mathrm{\tilde{C}} state below 1600 cm−1^{-1} of vibrational excitation. This enables a direct characterization of the vibrational level staggering that results from the double-minimum potential. In addition, it allows us to deperturb the strong cc-axis Coriolis interactions between levels of a1_1 and b2_2 vibrational symmetry, and to determine accurately the vibrational dependence of the rotational constants in the distorted C~\mathrm{\tilde{C}} electronic state.

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