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The Far-Infrared Fourier Transform Spectrum of H2Se

โœ Scribed by I.N. Kozin; S. Klee; P. Jensen; O.L. Polyansky; I.M. Pavlichenkov


Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
715 KB
Volume
158
Category
Article
ISSN
0022-2852

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โœฆ Synopsis


In the present work. we study the spectrum of the (\mathrm{H}{2} \mathrm{Se}) molecule in the far-infrared region. This work is a continuation of our experimental investigation of the anomalous "fourfold clustering effect" exhibited by the rotational energy levels in the vibrational ground state of (\mathrm{H}{2} \mathrm{Se}). The spectrum in the region (30-360 \mathrm{~cm}^{-1}) was measured with a Bruker IFS (120 \mathrm{HR}) interferometer attached to a 3 -m-long cell. In order to observe transitions involving high (J) and (K_{u}) quantum numbers the cell was heated to (90^{\circ} \mathrm{C}). About 2500 lines were identified and fitted using a modified Watson Hamiltonian. Improved sets of rotational and centrifugal distortion constants for all six selenium isotopomers were obtained. It is shown that the fourfold clustering of rotational levels, as well as the observed linestrength distortions, can be explained in terms of localized wavefunctions.
c. 1993 Academic Press. Ins


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