The IR absorption spectra of CO2 doped Xe solutions have been recorded in the range of the fundamental v(3)(Sigma (u)) band and of the Coriolis perturbed v(1) + v(2)(1), v(1) + v(2)(11) (pi (u)) Fermi doublet (v(1) + v(2) approximate to 3v(2)) in gas, liquid and solid phases. The characteristic transformation and rapid narrowing of the v(3) band, observed in the gas to liquid phase transition, shows marked hindering of the rotational motion of the CO2 molecule in dense Xe mixtures. It was found that the liquid to solid phase transition is accompanied by noticeable broadening of the v(3) band. The rotational motion of CO2 is not frozen in solid Xe at least near the freezing point. This is in contrast with sharp narrowing of the vibrational bands and so with blocking up rotations in the case of a heavier CS2 guest in the solid Xe host just below the freezing point. The intensity ratio A(v(1) + v(2)(1))/A(v(1) + v(2)(11)) of the Coriolis perturbed v(1) + v(2)(1), v(1) + v(2)(11) doublet reveals the noticeable increase from 8 +/- 1 in a low density gas to 18 +/- 2 in the liquid phase. The results obtained suggest remarkable modification of the second-order Coriolis coupling in the case of CO2 doped dense liquid Xe. (C) 2001 Elsevier Science B.V. All rights reserved.

Original languageEnglish
Pages (from-to)179-183
Number of pages5
JournalJournal of Molecular Structure
Volume596
DOIs
StatePublished - 26 Sep 2001
Event3rd International Conference of the Vibrational Spectroscopy in Materials Science - KRAKOW, Poland
Duration: 23 Sep 200026 Sep 2000

    Research areas

  • vibrational spectra, CO2, noble gas solutions, phase transition, rotational relaxation processes, Coriolis coupling

ID: 41409705