Issue 3, 1987

Infrared–radiofrequency double-resonance spectra and pressure broadening in the enantiomers and racemic mixture of gaseous 1,2-dichloro-2-fluoroethanone

Abstract

The frequencies and pressure broadening of some infrared–radiofrequency double-resonance absorptions are reported for the (–) enantiomer and racemic mixture of 1,2-dichloro-2-fluoroethanone at mTorr pressures. This is the first study of its kind, aimed at discerning spectral differences between an enantiomer and its racemic mixture at sub-Doppler resolution. The different frequency dependence of the lineshape in the enantiomer and racemic mixture as a function of pressure (i.e. collision rate) is a source of information on the statistical cross-correlation between vibration, rotation and translation during the intermolecular collision. Some differences in intensity have been found for the infrared–microwave double-resonance lines at 736 and 588 MHz on the 10 R32 CO2 laser line, but these differences could be due to chemical and/or absorption phenomena or to a genuine intensity difference between the enantiomer and the racemate. Another radio-frequency resonance at 273 MHz was also investigated and the results are given in this paper together with their equivalents in all three lines in the racemic mixture. This high-resolution spectroscopic investigation does not show with a clear level of confidence the differences expected from the different statistical correlation between vibration, rotation and translation in enantiomer and racemic mixture.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 2, 1987,83, 463-471

Infrared–radiofrequency double-resonance spectra and pressure broadening in the enantiomers and racemic mixture of gaseous 1,2-dichloro-2-fluoroethanone

D. Hennequin, P. Glorieux, E. Arimondo and M. W. Evans, J. Chem. Soc., Faraday Trans. 2, 1987, 83, 463 DOI: 10.1039/F29878300463

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