Hostname: page-component-78c5997874-fbnjt Total loading time: 0 Render date: 2024-11-14T23:49:23.905Z Has data issue: false hasContentIssue false

Molecular Data for Stellar Opacities

Published online by Cambridge University Press:  30 March 2016

Uffe Gråe Jørgensen*
Affiliation:
Niels Bohr Institute, Blegdamsvej 17, DK-2100 Copenhagen, Denmark

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

In total, 40 neutral diatomic molecules, 2 molecular ions, and 7 polyatomic molecules are known from observed photospheric stellar spectra. Line data for opacity computations (i.e., lists of line frequencies, intensities, and excitation energies) exist for 17 of these molecules, although the data are complete only for a handful of them. A detailed description of stellar photospheric molecules can be found in Tsuji (1986), and the existing opacity data have been reviewed by Jorgensen (1995).

Listed line frequencies in the data bases are either the measured values, or based on computed molecular constants obtained from fits to measured values. Attempts to compute ab initio line frequencies have so far resulted in lower accuracy than what is obtained by use of molecular constants. Published line strengths include measured values as well as ab initio values. For strong bands the ab initio intensities are as accurate as the laboratory values, whereas measured values for weak bands are generally more accurate than the ab initio values. The primary advantage of ab initio computations is therefore that the complete set of all transitions can be obtained. Exploratory studies have shown that completeness of the line data is crucial for the obtained stellar photospheric structure.

As an alternative to the ab initio computations of the line intensities, fits to experimental data have been attempted. The most promising method seems to be to fit the dipole function by use of a Padé approximant. Combined with a potential fitted to experimental energy levels, such a dipole function can in principle be used to predict the complete list of band intensities and line intensities for all bands with energies up to the molecular dissociation energy. The part of the dipole function which corresponds to the largest stretching (or bending) of the molecule is the most uncertain in such fits as well as in ab initio computations. This part is responsible for most of the many weak transitions, and large uncertainties are therefore to be excepted in the computed intensities of the weak spectral bands. As these are of major importance for the stellar photospheric structure (due to their huge number and their pseudo continuous appearance in the spectrum), a particularly large effort is desirable in comparing computed intensities with laboratory data for a representative sample of weak bands. Unfortunately, only few measurements of weak bands exist.

Type
II. Joint Discussions
Copyright
Copyright © Kluwer 1995

References

Borysow, A. 1994, in: Molecules in the Stellar Environment, Jorgensen, U.G. (ed.), Springer, p.209 Google Scholar
Brown, L.R., Farmer, C.B., Rinsland, C.P., Toth, R.A. 1987, Appl. Optics, 26, 5154 CrossRefGoogle Scholar
Davis, S.P. 1987, Publ. Astron. Soc. Pac., 99, 1105 CrossRefGoogle Scholar
Davis, S.P. 1994, in: Molecules in the Stellar Environment, Jorgensen, U.G. (ed.), Springer, p.397 Google Scholar
Husson, N., Bonnet, B., Scott, N.A., Chedin, A. 1991, Internal Note, Laboratoire de Meteorologie Dynamique. No. 163 Google Scholar
Jorgensen, U.G. 1995, in: Astrophysical Applications of Powerful New Atomic Databases, Adelman, S., Wiese, W. (eds.), ASP Conference Series, in pressGoogle Scholar
Jorgensen, U.G., Jensen, p. 1993, Mol, J.. Spectrosc, 161, 219 Google Scholar
Jorgensen, U.G., Larsson, M. 1990, A&A, 238, 424 Google Scholar
Kurucz, R.L. 1994, in: Molecules in the Stellar Environment, Jorgensen, U.G. (ed.), Springer, p.282 Google Scholar
Kurucz, R.L., Peytremann, E. 1975, SAO Spec. Rept., 362 Google Scholar
Kuznetsova, L.A., Pazyuk, E.A., Stolyarov, A.V. 1993, Russian, J. Phys. Chem., 67, 2046 Google Scholar
Langhoff, S.R., Bauschlicher, C.W. 1993, Chem. Phys. Lett., 211, 305 CrossRefGoogle Scholar
Littleton, J.E., Davis, S.P. 1985, ApJ, 296, 152 Google Scholar
Pineiro, A.L., Tipping, R.H., Chackerian, C. Jr. 1987a, J. Mol. Spec., 125, 91 Google Scholar
Pineiro, A.L., Tipping, R.H., Chackerian, C. Jr. 1987b, J. Mol. Spec., 125, 184 Google Scholar
Rothman, L.S., et al. 1992, JQSRT, 48, 469 CrossRefGoogle Scholar
Tsuji, T. 1986, ARA&A, 24, 411 Google Scholar
van Dishoeck, E.F. 1994, in: Molecules in the Stellar Environment, Jorgensen, U.G. (ed.),Google Scholar