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Observation of b2 symmetry vibrational levels of the SO2 C̃ (1)B2 state: Vibrational level staggering, Coriolis interactions, and rotation-vibration constants.
Park, G Barratt; Jiang, Jun; Saladrigas, Catherine A; Field, Robert W.
Afiliação
  • Park GB; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
  • Jiang J; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
  • Saladrigas CA; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
  • Field RW; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
J Chem Phys ; 144(14): 144311, 2016 Apr 14.
Article em En | MEDLINE | ID: mdl-27083725
ABSTRACT
The C̃ (1)B2 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 X̃ state are vibronically forbidden. We use IR-UV double resonance to observe the b2 vibrational levels of the C̃ 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 C̃ electronic state.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article