Escribano, R., Mills, I. and Brodersen, S. (1976) Second order Coriolis resonance in the v2, v5 Raman bands of CH3F. Journal of Molecular Spectroscopy, 61 (2). pp. 249-264. ISSN 0022-2852 doi: 10.1016/0022-2852(76)90247-2
Abstract/Summary
The vibration-rotation Raman spectrum of the ν2 and ν5 fundamentals of CH3F is reported, from 1320 to 1640 cm−1, with a resolution of about 0.3 cm−1. The Coriolis resonance between the two bands leads to many perturbation-allowed transitions. Where the resonance is still sufficiently weak that the quantum number K′ retains its meaning, perturbation-allowed transitions are observed for all values of ΔK from +4 to −4; in regions of strong resonance, however, we can only say that the observed transitions obey the selection rule Δ(k−l) = 0 or ±3. The spectrum has been analyzed by band contour simulation using a computer program based on exact diagonalization of the Hamiltonian within the ν2, ν5 vibrational levels, and improved vibration-rotation constants for these bands are reported. The relative magnitudes and relative sings of polarizability derivatives involved in these vibrations are also reported.
Altmetric Badge
Item Type | Article |
URI | https://reading-clone.eprints-hosting.org/id/eprint/7444 |
Item Type | Article |
Refereed | Yes |
Divisions | Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry |
Publisher | Academic Press |
Download/View statistics | View download statistics for this item |
University Staff: Request a correction | Centaur Editors: Update this record