Microwave Spectrum of the C3S Molecule in the Vibrationally Excited States of Bending Modes, v4 and v5

1995 ◽  
Vol 169 (1) ◽  
pp. 92-107 ◽  
Author(s):  
J.A. Tang ◽  
S. Saito
1985 ◽  
Vol 40 (9) ◽  
pp. 913-919
Author(s):  
Juan Carlos López ◽  
José L. Alonso

Abstract The rotational transitions of 3,4-dihydro-1,2-pyran in the ground state and six vibrationally excited states have been assigned. The rotational constants for the ground state (A = 5198.1847(24), B = 4747.8716(24) and C = 2710.9161(24) have been derived by fitting μa, μb and μc-type transitions. The dipole moment was determined from Stark displacement measurements to be 1.400(8) D with its principal axis components |μa| =1.240(2), |μb| = 0.588(10) and |μc| = 0.278(8) D. A model calculation to reproduce the ground state rotational constants indicates that the data are consistent with a twisted ring conformation. The average intensity ratio gives vibrational separations between the ground and excited states of the ring-bending and ring-twisting modes of ~ 178 and ~ 277 cm-1 respectively.


1978 ◽  
Vol 33 (2) ◽  
pp. 156-163 ◽  
Author(s):  
Harold Jones ◽  
Michio Takami ◽  
John Sheridan

The microwave spectrum of chloroacetylene in the ground and excited states has been investigated in the frequency range 15 to 306 GHz. Ground state rotational and nuclear quadrupole coupling constants for twelve isotopic species of chloroacetylene and accurate distortion constants were determined for two of these. The data allowed the rs-structure of chloroacetylene to be reconsidered and the internal consistency of this method of structure determination to be checked. Rotational spectra in five vibrationally excited states, with energy up to 700 cm-1 were observed for four different isotopic species and spectroscopic constants for these states were derived.


1981 ◽  
Vol 36 (11) ◽  
pp. 1239-1241
Author(s):  
H. Dreizier ◽  
D. Steffek

The microwave spectrum of gauche 1,2-difluoroethane w as investigated in the ground and five vibrationally excited states by a centrifugal distortion analysis.


2020 ◽  
Vol 640 ◽  
pp. L13 ◽  
Author(s):  
J. R. Pardo ◽  
C. Bermúdez ◽  
C. Cabezas ◽  
M. Agúndez ◽  
J. D. Gallego ◽  
...  

Observations of IRC +10216 with the Yebes 40 m telescope between 31 and 50 GHz have revealed more than 150 unidentified lines. Some of them can be grouped into a new series of 26 doublets, harmonically related with integer quantum numbers ranging from Jup = 54 to 80. The separation of the doublets increases systematically with J, that is to say, as expected for a linear species in one of its bending modes. The rotational parameters resulting from the fit to these data are B = 290.8844 ± 0.0004 MHz, D = 0.88 ± 0.04 Hz, and q = 0.1463 ± 0.0001 MHz. The rotational constant is very close to that of the ground state of HC9N. Our ab initio calculations show an excellent agreement between these parameters and those predicted for the lowest energy vibrationally excited state, ν19 = 1, of HC9N. This is the first detection, and complete characterization in space, of vibrationally excited HC9N. An energy of 41.5 cm−1 is estimated for the ν19 state. In addition, 17 doublets of HC7N in the ν15 = 1 state, for which laboratory spectroscopy is available, were detected for the first time in IRC +10216. Several doublets of HC5N in its ν11 = 1 state were also observed. The column density ratio between the ground and the lowest excited vibrational states are ≈127, 9.5, and 1.5 for HC5N, HC7N, and HC9N, respectively. We find that these lowest-lying vibrational states are most probably populated via infrared pumping to vibrationally excited states lying at ≈600 cm−1. The lowest vibrationally excited states thus need to be taken into account to precisely determine absolute abundances and abundance ratios for long carbon chains. The abundance ratios N(HC5N)/N(HC7N) and N(HC7N)/N(HC9N) are 2.4 and 7.7, respectively.


1978 ◽  
Vol 33 (11) ◽  
pp. 1312-1322
Author(s):  
S. O. Ljunggren ◽  
P. J. Mjöberg ◽  
J . E. Bäckvall

The microwave spectrum of 1-butene oxide in the gas phase has been studied in the frequency region 18.0-39.0 GHz. The spectrum observed arose from a rotamer with a dihedral H-C2-C3-C4 angle of 59° ± 1°. In addition to several Q-branch progressions the spectrum contained several long perpendicular RP and PR progressions. However, of the ground state lines, only the intermediate PR transitions showed internal rotation splittings that could be resolved to yield a barrier height of 3.02 kcal mol-1. The value derived from the line splittings of the first excited methyl torsional state was slightly higher (3.17 kcal mol-1) but must be regarded as being less reliable. The components of the dipole moment, the rotational constants, and the quartic and sextic centrifugal distortion coefficients for the ground state and three vibrationally excited states were determined.


1964 ◽  
Vol 14 (1-4) ◽  
pp. 27-52 ◽  
Author(s):  
Takeshi Oka ◽  
Kojiro Takagi ◽  
Yonezo Morino

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