OC(NH2)2, v1
urea, carbonic acid diamide, v1
Species tag 060533
Version1*
Date of EntryJan. 2023
ContributorH. S. P. Müller

Please note that the identities of the exited states are not known. They have been numbered from low energies to higher energies. This state is the lowest excited vibrational state. The next state is at about four times the energy !
The transition frequencies were taken from
(1) D. J. Tyree, T. W. Chapman, I. R. Medvedev, Z. Kisiel, 2022, J. Mol. Spectrosc. 390, Art. No. 111706.
The transition frequencies were judged conservatively and were adjusted from 50 to 35 kHz. A small number of lines with larger residuals was omitted. The parameter set differs slightly from that in (1). The calculations should be accurate enough for all observational purposes. Transition frequencies with calculated uncertainties larger than 0.2 MHz should be viewed with caution.
The partition function considers the ground vibrational state only. Vibrational correction factors have been derived. Please do note the caveats ! Spin-statistical weights of the ratio 13 : 11 were omitted as they are close to 1 : 1. In v1, Ka + Kc even and odd would carry the weights of 13 and 11, respectively.
The ground state dipole moment was determined in
(2) R. D. Brown, P. D. Godfrey, and J. Storey, 1975, J. Mol. Spectrosc. 58, 445.

Lines Listed12929
Frequency / GHz< 1000
Max. J91
log STR0-8.0
log STR1-6.0
Isotope Corr.-0.0
Egy / cm–1~61.
 µa / D 
 µb / D3.83
 µc / D 
 A / MHz11208.967
 B / MHz10361.077
 C / MHz5419.071
 Q(300.0)34925.8391
 Q(225.0)22682.8934
 Q(150.0)12345.3379
 Q(75.00)4365.7721
 Q(37.50)1545.0571
 Q(18.75)547.4806
 Q(9.375)194.4567
 Q(5.000)76.3590
 Q(2.725)31.1779
detected in ISM/CSMyes


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