High-resolution spectrum of the first triad of D2 32S interacting states
OPTICS AND SPECTROSCOPY
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The high-resolution spectrum of the D2S molecule registered with a Bruker IFS 120HR Fourier spectrometer in the range 2000–4200 cm–1 is analyzed. The spectroscopic parameters of the (110), (011), and (030) vibrational states are obtained. They reproduce rotational energy levels with the accuracy close to experimental one (a total of 737 rovibrational energies is considered corresponding to 2590 transitions up to J max = 21).
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rovibrational spectra spectroscopic parameters inverse spectroscopic problemPreview
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References
- 1.C. Vastel, T. G. Phillips, C. Ceccarelli, and J. Pearson, Astrophys. J., 593, L97–L100 (2003).CrossRefADSGoogle Scholar
- 2.L. Halonen and T. Carrington, Jr., J. Chem. Phys., 88, 4171–4185 (1988).CrossRefADSGoogle Scholar
- 3.I. N. Kozin and P. Jensen, J. Mol. Spectrosc., 163, 483–509 (1994).CrossRefADSGoogle Scholar
- 4.O. Polyansky, P. Jensen, and J. Tennyson, Ibid., 178, 184–188 (1996).Google Scholar
- 5.Vl. G. Tyuterev, S. A. Tashkun, and D. W. Schwenke, Chem. Phys. Lett., 348, 223–234 (2001).CrossRefADSGoogle Scholar
- 6.Vl. G. Tyuterev, L. Régalia-Jarlot, D. W. Schwenke, et al., Physique, 5, 189–199 (2004).CrossRefADSGoogle Scholar
- 7.T. Cours, P. Rosmus, and Vl. G. Tyuterev, Chem. Phys. Lett., 331, 317–322 (2000).CrossRefADSGoogle Scholar
- 8.T. Cours, P. Rosmus, and Vl. G. Tyuterev, J. Chem. Phys., 117, 5192–5208 (2002).Google Scholar
- 9.G. Tarczay, A. Csaszar, M. Leininger, and W. Klooper, Chem. Phys. Lett., 322, 119–128 (2000).CrossRefADSGoogle Scholar
- 10.C. R. Bailey, J. W. Thompson, and J. Hale, J. Chem. Phys., 4, 625–631 (1936).CrossRefADSGoogle Scholar
- 11.A. H. Nielsen and H. H. Nielsen, J. Chem. Phys., 5, 277–283 (1937).CrossRefADSGoogle Scholar
- 12.H. C. Allen, R. E. Naylor, and E. K. Plyler, J. Res. Natl. Bur. Stand., 53, 321–323 (1954).Google Scholar
- 13.H. C. Allen, E. K. Plyler, and R. L. Blaine, Ibid., 59, 211–214 (1957).Google Scholar
- 14.R. E. Miller, G. E. Leroi, and D. F. Eggers, J. Chem. Phys., 45, 3028–3037 (1966).CrossRefADSGoogle Scholar
- 15.R. E. Miller, G. E. Leroi, and D. F. Eggers, Ibid., 46, 2292–2297 (1966).Google Scholar
- 16.R. L. Cook, F. C. De Lucia, and P. Helminger, J. Mol. Spectrosc., 4, 123–136 (1974).Google Scholar
- 17.J. L. Gillis, R. D. Blatherwick, and F. S. Bonomo, Ibid., 114, 228–233 (1985).Google Scholar
- 18.C. Camy-Peyret, J.-M. Flaud, L. Lechuga-Fossat, and J. W. C. Johns, J. Mol. Spectrosc., 109, 300–333 (1985).CrossRefADSGoogle Scholar
- 19.C. Camy-Peyret, J.-M. Flaud, A. N’Gom, and J. W. S. Johns, Mol. Phys., 65, 649–657 (1988).CrossRefADSGoogle Scholar
- 20.O. N. Ulenikov, R. N. Tolchenov, E. N. Melekhina, et al., J. Mol. Spectrosc., 170, 397–416 (1995).CrossRefADSGoogle Scholar
- 21.L. S. Rothman, D. Jacquemart, A. Barbe, et al., J. Quant. Spectrosc. Radiat. Transfer, 96, 139–204 (2005).CrossRefADSGoogle Scholar
- 22.J. K. G. Watson, J. Chem. Phys., 46, 1935–1949 (1967).CrossRefADSGoogle Scholar
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