Journal
JOURNAL OF MOLECULAR SPECTROSCOPY
Volume 352, Issue -, Pages 1-9Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jms.2018.07.005
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Funding
- Polish National Science Centre [DEC/2011/02/A/ST2/00298]
- MINECO [CTQ2017-89150-R]
- UPV/EHU [UFI11/23, PPG17/10]
- FPU contract from the MECD
- ERDF
- ESF
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The pure rotational spectrum of CF3CCl3 (1,1,1-trichloro-2,2,2-trifluoroethane, CFC-113a) was investigated at 4-18 GHz in supersonic expansion with chirped pulse and cavity Fourier -transform rotational spectroscopy, and at 94-309 GHz with broadband millimetre wave spectroscopy. Spectroscopic constants for all four possible chlorine isotopic species have been considerably updated. Global fits of hyperfine -resolved and hyperfine -unresolved data are reported and triple chlorine nucleus hyperfine structure has been analysed for all four isotopologues to within experimental accuracy. The new measurements have been augmented with anharmonic force field calculations in an evaluation of the semi -experimental equilibrium geometry for CF3CCl3. Interactions between hyperfine sublevels contributing to frequencies of the lowest J transitions allowed determination of the axial rotational constant A = 1326.24(15) MHz for (CF3CCl3)-Cl-35 from analysis of pure rotational transitions. (C) 2018 Elsevier Inc. All rights reserved.
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