O13CS
Carbonyl sulfide, 13C isotopomer
Species tag 061502
Version1*
Date of EntryApr. 2005
ContributorH. S. P. Müller

The experimental lines are from
(1) N. W. Larsen, and B. P. Winnewisser, 1974, Z. Naturforsch. 29a, 1213; from
(2) A. Dubrulle, J. Demaison, J. Burie, and D. Boucher, 1980, Z. Naturforsch. 35a, 471; from
(3) J. P. M. de Freede, M. P. W. Gillis, and H. A. Dijkerman, 1988, J. Mol. Spectrosc. 128, 509; and from
(3) F. J. Lovas and R. D. Suenram, 1987, J. Chem. Phys. 87, 2010.
Predictions beyond J = 50 should be viewed with some caution.
The 13C nuclear spin-rotation splitting may be resolved for the J = 1 – 0 transition; the splitting is about 5.1 kHz for this transition with an intensity ratio of 1 : 2. This splitting is unlikely to be resolved for higher J because it is only about 3.4 kHz between the strong hfs components. The 13C spin multiplicity of 2 was not considered in the calculation of the partition function !
The dipole moment is from
(4) K. Tanaka, T. Tanaka, and I. Suzuki 1985, J. Chem. Phys. 82, 2835.

Lines Listed99
Frequency / GHz< 1196
Max. J99
log STR0-6.5
log STR1-5.7
Isotope Corr.-1.994
Egy / (cm-1)0.0
 µa / D0.7153
 µb / D 
 µc / D 
 A / MHz 
 B / MHz6061.92
 C / MHz 
 Q(500.0)1720.2448
 Q(300.0)1031.9755
 Q(225.0)773.9794
 Q(150.0)516.0405
 Q(75.00)258.1586
 Q(37.50)129.2392
 Q(18.75)64.7853
 Q(9.375)32.5604
detected in ISM/CSMyes


Database maintained by Holger S. P. Müller and Sven Thorwirth, programming by D. Roth and F. Schlöder