Observation of b2 symmetry vibrational levels of the SO2 C ̃ 1B2 state: Vibrational level staggering, Coriolis interactions, and rotation-vibration constants
The C ̃ 1B2 state of SO2 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 vibrational symmetry) have not previously been observed bec...
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Veröffentlicht in: | The Journal of chemical physics 2016-04, Vol.144 (14) |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The
C
̃
1B2 state of SO2 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 vibrational symmetry) have not previously been observed because transitions into these levels from the zero-point level of the
X
̃
state are vibronically forbidden. We use IR-UV double resonance to observe the b2 vibrational levels of the
C
̃
state below 1600 cm−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 c-axis Coriolis interactions between levels of a1 and b2 vibrational symmetry and to determine accurately the vibrational dependence of the rotational constants in the distorted
C
̃
electronic state. |
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ISSN: | 0021-9606 1089-7690 |
DOI: | 10.1063/1.4944924 |