A plethora of vibrational states of the HCN molecule are of
relevance for astronomical observations.
The states are designated by
(v1v2v3).
Note: The
(100) mode is the CH stretching mode at
3311.5 cm1; the (010) mode
is the doubly degenerate bending mode at
712.0 cm1; and the (001) mode is the CN
stretching mode at 2096.8 cm1.
The designation of the (100) and (001) modes has been
interchanged on occasion sometimes without recognizing
this.
The Feb. 2003 entry was based on data for (000) and (010).
The May 2007 entry employs in addition data for
(020) and (030) as well as (001) and (100).
Below (100), the Coriolis interacting (040) and (011) states
have to be included in the fit.
The observed v = 0 transitions were summarized largely
in
(1) V. Ahrens, F. Lewen, S. Takano, G. Winnewisser, S. Urban,
A. A. Negirev, and A. N. Koroliev,
2002, Z. Naturforsch., 57a, 669.
One additional high J transition was reported
in
(2) S. Thorwirth, H. S. P. Müller, F. Lewen, S. Brünken,
V. Ahrens, and G. Winnewisser,
2003, Astrophys. J. 585, L163.
For the May 2007 entry the J = 2 1
transition frequencies were taken from
(3) G. Cazzoli and C. Puzzarini, unpublished;
cited in A. V. Lapinov,
2006, Proc. SPIE 6580, Art. No. 658001.
Sources for the v2 = 1 data are given in
e027503.cat, those for higher vibrational states in one of the
documentations e027507.cat to e027510.cat.
Extensive infrared data was taken from
(4) A. G. Maki, G. C. Mellau, S. Klee, M. Winnewisser, and W. Quapp,
2000, J. Mol. Spectrosc. 202, 67.
The dipole moment was reported by
(5) W. L. Ebenstein and J. S. Muenter,
1984, J. Chem. Phys. 80, 3989.
The 14N hyperfine splitting can be resolved for low values
of J. Therefore, a separate
hyperfine calculation is provided up to J" = 10
up to 1 THz.
While the general entries do NOT include hyperfine effects,
the spin multiplicity gI of 3 for the
14N nucleus is included in the partition function
as well as in the upper state degeneracy gup.
The partition function takes into account all vibrational states
used in the fit.
Contributions of individual vibrational states to the partition
function are available. The vibrational contributions are essentially
complete at 300 K.
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