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Rotational Spectra of 13CH3F in the v2 = 1 and v5 = 1 Vibrational States

✍ Scribed by D. Papousek; J. Demaison; G. Wlodarczak; J. Cosleou; P. Pracna; S. Klee; M. Winnewisser; S.P. Belov; M.Y. Tretyakov


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
666 KB
Volume
164
Category
Article
ISSN
0022-2852

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✦ Synopsis


Millimeter-wave and submillimeter-wave spectra of the rotational transitions in the (v_{2}=1) and (v_{5}=1) vibrational states of ({ }^{13} \mathrm{CH}{3} \mathrm{~F}) were measured up to (462 \mathrm{GHz}). Far-infrared spectra of these transitions were measured in the region (30-65 \mathrm{~cm}^{-1}) with a resolution of (0.0019 \mathrm{~cm}^{-1}) using an interferometric spectrometer Bruker IFS 120 HR. Almost 700 lines including 14 lines of the (\Delta\left(k-l{s}\right)= \pm 3) perturbation-allowed transitions in the (v_{s}=1) state were assigned. Both vibrational states are strongly perturbed, especially by the (x, y)-Coriolis resonance and "2, -1 " 1 -type interactions. The corresponding spectroscopical parameters were determined by a nonlinear leastsquares fit to the experimental data. (c) 1994 Academic Press, Inc.


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A representation of the effective rotational Hamiltonian in the form of optimum versions of a rational series of the perturbation theory is suggested for nonisolated molecular states. This representation is used to analyze the most complete set of precise transition frequencies in the rotational spe