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Title: Observation of b2 symmetry vibrational levels of the SO2C 1B2 state: Vibrational level staggering, Coriolis interactions, and rotation-vibration constants

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4944924· OSTI ID:1248484

The $$\tilde{C}$$ 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 $$\tilde{X}$$ state are vibronically forbidden. We use IR-UV double resonance to observe the b2 vibrational levels of the $$\tilde{C}$$ 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 $$\tilde{C}$$ electronic state.

Research Organization:
Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
FG02-87ER13671
OSTI ID:
1248484
Alternate ID(s):
OSTI ID: 1247601; OSTI ID: 1733330; OSTI ID: 1831804
Journal Information:
Journal of Chemical Physics, Vol. 144, Issue 14; ISSN 0021-9606
Publisher:
American Institute of Physics (AIP)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 11 works
Citation information provided by
Web of Science

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