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Rovibrational spectroscopy of the Fermi-interacting nu(4)=1 and nu(3) = nu(6)=1 levels of DCF3

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    SYSNO ASEP0341550
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleRovibrational spectroscopy of the Fermi-interacting nu(4)=1 and nu(3) = nu(6)=1 levels of DCF3
    Author(s) Pracna, Petr (UFCH-W)
    Ceausu-Velcescu, A. (FR)
    Predoi-Cross, A. (CA)
    Urban, Š. (CZ)
    Source TitleJournal of Molecular Spectroscopy. - : Elsevier - ISSN 0022-2852
    Roč. 259, č. 1 (2010), s. 1-10
    Number of pages10 s.
    Languageeng - English
    CountryUS - United States
    Keywordsdeuterated fluoroform ; high resolution IR spectroscopy ; anharmonic and vibration-rotation resonances
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsIAA400400706 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    LC06071 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000273967300001
    DOI10.1016/j.jms.2009.09.007
    AnnotationThe high-resolution infrared spectrum of deuterated fluoroform (DCF3) Was studied in the 700 and 1200 cm(-1) regions, with the aim of assigning and analyzing the nu(4) CF3 asymmetric stretching vibration. The Fermi-type anharmonic coupling between the nu(4) = 1 and nu(3) = nu(6) = 1 rovibrational levels, already mentioned in an early work of Ruoff et al. [Spectrochimica Acta Part A 31A (1975) 1099-1100], was studied here for the first time under high resolution. Assignments in the nu(3) + nu(6)/nu(4) band system were confirmed and extended by the identification of the nu(3) + nu(6) - nu(6) and nu(4)-nu(6) bands in the 700 cm(-1) region, the latter being enhanced near the Fermi crossings of the studied levels. Data from both the hot and difference bands were included in the analysis. The close separation of the studied vibrational levels of about 14.8 cm(-1) produces a large variety of resonance crossings which involve levels with Delta k = 0,..., 6.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2011
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