New Infrared Spectra of Acetylene-Water Dimers: First Determination of the A Rotational Constant and Another K -Dependent Anomaly

Infrared spectra of acetylene-water complexes are studied in the regions of the H O ν bend (1600 cm ) and the D O ν /ν stretches (2670-2808 cm ), using tunable infrared sources to probe a pulsed supersonic slit jet expansion. In the H O bend region, there is a puzzling absence of = 0 transitions for...

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Veröffentlicht in:The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2024-09, Vol.128 (36), p.7628-7633
Hauptverfasser: Barclay, A J, McKellar, A R W, Moazzen-Ahmadi, N
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Sprache:eng
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Zusammenfassung:Infrared spectra of acetylene-water complexes are studied in the regions of the H O ν bend (1600 cm ) and the D O ν /ν stretches (2670-2808 cm ), using tunable infrared sources to probe a pulsed supersonic slit jet expansion. In the H O bend region, there is a puzzling absence of = 0 transitions for C H -H O, while both = 0 and 1 are observed for C D -H O. This continues a pattern of "missing" states noted in previous infrared studies of acetylene-water. Noticeable line broadening gives estimates of upper state predissociation lifetimes of about 1.6 ns for C D -H O with = 1, 0.8 ns for C H -H O with = 1, and 0.8 ns for C D -H O with = 0. The lifetime for C H -H O = 0 must be much shorter (
ISSN:1089-5639
1520-5215
1520-5215
DOI:10.1021/acs.jpca.4c04599