The (0, 0) band of the A 4 ⌸-X 4 ⌺ Ϫ transition of MoN, between 590 and 635 nm, has been studied using the sub-Doppler technique of intermodulated laser-induced fluorescence spectroscopy. Spectra taken at a resolution of about 60 MHz showed resolved hyperfine structure, which is caused principally b
A Reinvestigation of the c3Π–X1Σ+ (0–0) Absorption Band of Carbon Monoxide
✍ Scribed by Jacob Baker; Françoise Launay; Michéle Eidelsberg; François Rostas
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 199 KB
- Volume
- 203
- Category
- Article
- ISSN
- 0022-2852
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✦ Synopsis
The forbidden c 3 ⌸-X 1 ⌺ ϩ (0-0) absorption band of carbon monoxide has been reinvestigated under different pressure conditions using the 10.7-m VUV spectrograph at Meudon. Overlap with the allowed C 1 ⌸-X 1 ⌺ ϩ (0-0) band at lower transition energy has been taken into account. We have identified a new rotational branch corresponding to an S-type branch and extended the analysis to both higher and lower J. An analysis of the band structure and the low J transition lines suggests that the band gains its intensity predominantly as a result of an interaction of the c 3 ⌸ state with a 1 ⌺ ϩ state, most likely the C 1 ⌺ ϩ (v ϭ 0) state. Molecular constants have been obtained for the c 3 ⌸ state that are in reasonable agreement with those previously published. The apparently anomalous small value for the centrifugal distortion constant is explained by a homogeneous perturbation with the k 3 ⌸ valence state.
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