Abstract
The B state of SO 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 (b vibrational symmetry) have not previously been observed because transitions into these levels from the zero-point level of the state are vibronically forbidden. We use IR-UV double resonance to observe the b vibrational levels of the state below 1600 cm 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 -axis Coriolis interactions between levels of a and b vibrational symmetry, and to determine accurately the vibrational dependence of the rotational constants in the distorted electronic state.
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