The H2S spectrum around 0.7 μm

被引:27
作者
Flaud, JM
Vaittinen, O
Campargue, A
机构
[1] Univ Paris 11, CNRS, Photophys Mol Lab, F-91405 Orsay, France
[2] Univ Grenoble 1, Spectrometrie Phys Lab, CNRS, UMR5588, F-38402 St Martin Dheres, France
关键词
D O I
10.1006/jmsp.1998.7581
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The overtone spectrum of H2S has been recorded by intracavity laser spectroscopy in the 14100-14400 cm(-1) spectral region. The rovibrational analysis was performed allowing one to assign not only lines involving the pair of interacting states {(402), (303)} {(60(+), 0), (60(-), 0)} in local mode notation), but also lines involving the interacting states {(322), (223)} ({(50(+), 2.), (50(-), 2)} in local mode notation). Indeed, apart from the strong H-22 interactions that link the rotational levels of the states (60(+/-), 0) on the one hand, and the rotational levels of the states (50(+), 2) on the other hand, we observe that the rotational levels of the two pairs of states interact strongly through anharmonic and Coriolis-type resonances. These resonances transfer intensity to lines involving the (50+, 2) pair of states. Altogether 80 rotational upper-state levels have been observed and reproduced satisfactorily using an Hamiltonian matrix that takes explicitly into account the various interactions and assumes the same vibrational energy and rotational constants for the two components of the local mode pairs. The following band centers have been obtained: v(o) (60(+), 0) = 14291.122 cm(-1) and v(o) (50(+/-), 2) = 14284.705 cm(-1). Finally a local mode-type behavior is evidenced by the values of the Hamiltonian constants, and refined vibrational local mode parameters are obtained. (C) 1998 Academic Press.
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页码:262 / 268
页数:7
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