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The Far Infrared Spectrum of the NO Dimer

โœ Scribed by A.R.W. McKellar; J.K.G. Watson


Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
145 KB
Volume
194
Category
Article
ISSN
0022-2852

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โœฆ Synopsis


The far-infrared spectrum of the NO dimer in the gas phase has been observed for the first time using a long-path (180 m) cooled (99 K) absorption cell and a Bomem Fourier transform spectrometer. Four weak vibration-rotation bands were detected in the 120 -450 cm ฯช1 region and assigned to intermolecular vibrations of the cis-planar ON-NO complex. The strongest is a type b band at 239.36 cm ฯช1 , which is assigned as the 2 (symmetric bending) fundamental. A second type b band at 134.50 cm ฯช1 , partly obscured by 2 โŒธ 3/2 4 2 โŒธ 1/2 transitions of the NO monomer, is assigned as the 3 (intermolecular stretch) fundamental. A third type b band at 351.38 cm ฯช1 can then be assigned as the 2 ฯฉ 3 combination band. Finally, a very weak type a band at 429.14 cm ฯช1 is assigned as the 6 (antisymmetric bending) fundamental. We report here detailed analyses of the 2 and 2 ฯฉ 3 bands, which yielded upper state rotational parameters, centrifugal distortion parameters, and band origins. Somewhat less extensive analyses for 3 and 6 give their rotational parameters and band origins. These results resolve the mystery of the true values of the intermolecular vibrational frequencies of the NO dimer, which turn out to be rather different from previous determinations based on condensed phase spectra.


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