Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5415530 | Journal of Molecular Spectroscopy | 2009 | 7 Pages |
Abstract
Rotationally resolved spectra of the AË2Aâ²-XË2Aâ³ system for the HSO radical were observed by laser induced fluorescence spectroscopy. The radical was produced in a discharged supersonic jet of a gas mixture of dimethyl disulfide and O2 diluted in Ar. The observed spectra were assigned to ro-vibronic transitions of the Kaâ²âKaâ³Â = 0 â 1, 1 â 0, and 2 â 1 subbands of AË(00v3â²)-XË (0 0 0) with v3â²Â = 0-8, and those of AË (0 1 3) â XË (0 0 1), yielding the rotational and spin-rotation interaction constants for the excited electronic state. For the vibronic origin band, the band origin and the rotational constants are determined to be Tv = 14383.2533(28) cmâ1, A = 287316(33), (B + C)/2 = 16712.8(48), and (B â C)/2 = 532.0(70) MHz. Dispersed fluorescence spectra of the HSO radical were also observed, where the fundamental vibrational frequencies of the ν1 and ν2 modes for the XË state have been determined experimentally for the first time.
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Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Takashi Yoshikawa, Akihiro Watanabe, Yoshihiro Sumiyoshi, Yasuki Endo,