C4H, v5 = 1
Butadiynyl, v5 = 1, 2Πi
Species tag 049515
Version1*
Date of EntryFeb. 2020
ContributorH. S. P. Müller

Transition frequencies were reported by
(1) A. L. Cooksy, C. A. Gottlieb, T. C. Killian, P. Thaddeus, N. A. Patel, K. H. Young, and M. C. McCarthy, 2015, Astrophys. J. Suppl. Ser. 216, Art. No. 30.
Hyperfine parameters could not be determined. Values were guessed for the present entry based on data for other vibrational states. The HFS splitting, especially at low frequencies, should be viewed with considerable caution. Transition frequencies with calculated uncertainties exceeding 0.1 MHz should be viewed with caution.
The vibrational energy was taken from a quantum chemical calculation by
(2) S. Graf, J. Geiss, and S. Leutwyler, 2001, J. Chem. Phys. 114, 4542.
The dipole moment was assumed to be the same as in the X 2Σ+ ground vibrational state, see e049503.cat. This assumption may be reasonable.
The partition function of the main species takes into account all states presently available in the CDMS. It is converged fairly well up to about 150 K. Vibrational contributions to the partition function are also available. These should be viewed cautiously because of several estimates concerning vibrational energies.

Lines Listed488
Frequency / GHz< 600
Max. J62
log STR0-8.5
log STR1-5.3
Isotope Corr.-0.0
Egy / (cm–1)578
 µa / D2.1
 µb / D 
 µc / D 
 A / MHz 
 B / MHz4778.035
 C / MHz 
 Q(300.0)15542.2130
 Q(225.0)8848.3936
 Q(150.0)4095.2962
 Q(75.00)1420.6195
 Q(37.50)660.0312
 Q(18.75)329.7446
 Q(9.375)165.5392
 Q(5.000)88.9165
 Q(2.725)49.0805
detected in ISM/CSMno


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