cis-HC(O)SH
Monothioformic acid, cis isomer
Species tag 062516
Version1*
Date of EntryApr. 2014
ContributorH. S. P. Müller

Among the four possible isomers of monothioformic acid, trans-HC(O)SH and cis-HC(O)SH are stable, whereas trans-HC(S)OH and cis-HC(S)OH are not. As for formic acid, the cis isomer is higher than the trans isomer. The experimental lines were reported by
(1) W. H. Hocking and G. Winnewisser, 1976, Z. Naturforsch. 31a, 422.
Predictions with calculated uncertainties larger than 200 kHz should be viewed with caution. The data set is probably extensive enough for astronomical observations.
The dipole moment and the energy difference were determined in
(2) W. H. Hocking and G. Winnewisser, 1976, Z. Naturforsch. 31a, 995.
The energy difference of 231.3 cm–1 and the separating barrier are high enough that the two isomers may exist as seperate molecules at low to moderately high temperatures (below 100 K). The partition functions were therefore determined independently.

Lines Listed8974
Frequency / GHz< 1000
Max. J103
log STR0-8.3
log STR1-6.5
Isotope Corr.-0.028
Egy / (cm–1)0.0
 µa / D1.805
 µb / D2.228
 µc / D 
 A / MHz62927.71
 B / MHz6134.261
 C / MHz5584.754
 Q(300.0)18918.4802
 Q(225.0)12281.6150
 Q(150.0)6682.4965
 Q(75.00)2362.5784
 Q(37.50)836.0380
 Q(18.75)296.2456
 Q(9.375)105.2335
detected in ISM/CSMno


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