High resolution study of the v1+2v2-v2 and 2v2+v3-v2 "hot" bands and ro-vibrational re-analysis of the v1+v2/v2+v3/3v2 polyad of the32SO2 molecule / O. N. Ulenikov [et al.]

Уровень набора: Journal of Quantitative Spectroscopy and Radiative TransferАльтернативный автор-лицо: Ulenekov (Ulenikov), O. N., physicist, Professor of Tomsk Polytechnic University, Doctor of physical and mathematical sciences, 1949-, Oleg Nikolaevich;Gromova, O. V., physicist, Engineer-Researcher of Tomsk Polytechnic University, Candidate of physical and mathematical sciences, 1982-, Olga Vasilievna;Bekhtereva, E. S., physicist, Professor of Tomsk Polytechnic University, Doctor of physical and mathematical sciences, 1974-, Elena Sergeevna;Bolotova, I. B., physicist, Technician of Tomsk Polytechnic University, 1989-, Irina Batorovna;Leroy, K. A., physicist, Junior researcher at Tomsk Polytechnic University, candidate of physico-mathematical Sciences, Professor, University of Montreal (France), 1961-, Klod (Claude) Andre;Horneman, V.-M.;Alanko, S.Язык: английский.Страна: .Резюме или реферат: The weak “hot” absorption bands, ν1+2ν2−ν2 and 2ν2+ν3−ν2, were analysed with high resolution using the Fourier transform interferometer Bruker IFS-120 HR. In order to make possible an analysis of theν1+2ν2−ν2 and 2ν2+ν3−ν2 bands, as the first step, we re-analysed considerably the stronger “cold” bands, ν1+ν2 and ν2+ν3, which are located in the same spectral regions. As the result of analysis we obtained about 2650 and 2050 transitions (1069 and 1001 upper state ro-vibrational energy values) withJmax. = 78, Kamax. = 27 and Jmax. = 68, Kamax. = 24 for the bands ν1+ν2 and ν2+ν3, respectively, that is considerably higher than in the earlier studies of corresponding bands (Jmax. = 33, Kamax. = 7 and Jmax. = 50,Kamax. = 16 for the same bands, ν1 ν2 and ν2+ν3, respectively). A strong local resonance interaction with the 3ν2 band was taken into account, and the set of parameters that reproduce the initial experimental data with an accuracy close to experimental uncertainties, was obtained. The weak ν1+2ν2−ν2 and2ν2+ν3−ν2 bands were assigned, and about 870 and 930 transitions (553 and 540 upper state ro-vibrational energy values) with Jmax. = 60 and Kamax. = 20 and Jmax. = 59 and Kamax. = 16 were assigned to the ν1+2ν2−ν2 and 2ν2+ν3−ν2 bands, respectively. A complete list of assigned transitions is presented, and corresponding spectroscopic parameters are obtained from the fit of assigned transitions (upper energy values)..Примечания о наличии в документе библиографии/указателя: [References: p. 511-512 (47 tit.)].Аудитория: .Тематика: электронный ресурс | труды учёных ТПУ Ресурсы он-лайн:Щелкните здесь для доступа в онлайн
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[References: p. 511-512 (47 tit.)]

The weak “hot” absorption bands, ν1+2ν2−ν2 and 2ν2+ν3−ν2, were analysed with high resolution using the Fourier transform interferometer Bruker IFS-120 HR. In order to make possible an analysis of theν1+2ν2−ν2 and 2ν2+ν3−ν2 bands, as the first step, we re-analysed considerably the stronger “cold” bands, ν1+ν2 and ν2+ν3, which are located in the same spectral regions. As the result of analysis we obtained about 2650 and 2050 transitions (1069 and 1001 upper state ro-vibrational energy values) withJmax. = 78, Kamax. = 27 and Jmax. = 68, Kamax. = 24 for the bands ν1+ν2 and ν2+ν3, respectively, that is considerably higher than in the earlier studies of corresponding bands (Jmax. = 33, Kamax. = 7 and Jmax. = 50,Kamax. = 16 for the same bands, ν1 ν2 and ν2+ν3, respectively). A strong local resonance interaction with the 3ν2 band was taken into account, and the set of parameters that reproduce the initial experimental data with an accuracy close to experimental uncertainties, was obtained. The weak ν1+2ν2−ν2 and2ν2+ν3−ν2 bands were assigned, and about 870 and 930 transitions (553 and 540 upper state ro-vibrational energy values) with Jmax. = 60 and Kamax. = 20 and Jmax. = 59 and Kamax. = 16 were assigned to the ν1+2ν2−ν2 and 2ν2+ν3−ν2 bands, respectively. A complete list of assigned transitions is presented, and corresponding spectroscopic parameters are obtained from the fit of assigned transitions (upper energy values).

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