First high-resolution analysis of the 1, 3 and 1 + 3 bands of sulphur dioxide 33S16O2

被引:15
|
作者
Flaud, J. -M. [1 ,2 ]
Blake, T. A. [3 ]
Lafferty, W. J. [4 ]
机构
[1] Univ Paris Est Creteil, UMR CNRS, Inst Pierre Simon Laplace, LISA, Creteil, France
[2] Univ Paris Diderot, UMR CNRS, Inst Pierre Simon Laplace, LISA, Creteil, France
[3] Pacific Northwest Natl Lab, Richland, WA USA
[4] NIST, Sensor Sci Div, Gaithersburg, MD 20899 USA
关键词
High-resolution infrared; 33S16O2 sulphur dioxide; molecular parameters; ROTATIONAL SPECTRUM; SULFUR-DIOXIDE; LINE-INTENSITIES; SO2; BANDS; (SO2)-S-32-O-18; SPECTROSCOPY; REANALYSIS; STATES;
D O I
10.1080/00268976.2016.1269966
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
HighlightsHigh-resolution spectra of (SO2)-S-33-O-16 have been recorded for the first time in the 8 and 4 mu m spectral regions.The (1), (3) and (1) + (3) bands of the (SO2)-S-33-O-16 have been analysed up to very high quantum numbers.Accurate ro-vibrational upper states constants have been determined. ABSTRACTFourier transform spectra of sulphur dioxide (SO2)-S-33-O-16 have been recorded in the 8.0 and 4.0 mu m spectral regions at a resolution of 0.0015 cm(-1) using a Bruker IFS 125HR spectrometer leading to the observation of the (1), (3) and (1) + (3) vibrational bands of the (SO2)-S-33-O-16 molecule. The corresponding upper state ro-vibrational levels were fit using a Hamiltonian matrix taking into account a Coriolis K-a = 3 resonance between the ro-vibrational levels of the 1(1) and 3(1) vibrational states and a Watson-type Hamiltonian for the ro-vibrational levels of the 1(1) 3(1) vibrational state. In this way it was possible to reproduce the upper state ro-vibrational levels to within the experimental uncertainty; i.e. approximate to 0.20 x 10(-3) cm(-1). Very accurate rotational and centrifugal distortion constants were derived from the fit together with the following band centres: (0) ((1)) = 1147.979535(60) cm(-1), (0) ((3)) = 1353.335912(60) cm(-1) and (0) ((1) + (3)) = 2487.493732(30) cm(-1). [GRAPHICS]
引用
收藏
页码:447 / 453
页数:7
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