Abstract

Infrared spectra (0.003 cm-1 resolution) of 16O16O18O and 16O18O18O ozone isotopologues have been recorded and analyzed in the range 600–5000 cm-1. Several thousand rovibrational lines belonging to 32 absorption bands have been measured and assigned. An accurate determination of band centers through the rovibrational analysis has been done, 12 bands being observed for the first time to our knowledge. In addition to atmospheric retrieval applications, these results are also useful for a validation of potential energy surfaces and for the study of isotope effects in dynamic processes of ozone.

© 2003 Optical Society of America

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  1. M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, A. Chichery, M. T. Bourgeois, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1 lines positions,” J. Mol. Spectrosc. 216, 454–464 (2002).
    [CrossRef]
  2. M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “Infrared spectrum of 16O18O16O in the 5μm range. Positions, intensities and atmospheric applications,” Atm. Optics Ocean, 16, 206–211 (2003).
  3. M. R. De Backer-Barilly, A. Barbe, S. A. Tashkun, Vl. G. Tyuterev, A. Chichery, “The 5ν3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O,” Mol. Phys. 22, 3499–3506 (2002).
    [CrossRef]
  4. M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1. Line positions,” J. Mol. Spectrosc. (2003), in press.
  5. Vl. G. Tyuterev, A. Barbe, S. N. Mikhailenko, Y. Babykov, “Spectroscopy and molecular properties of ozone,” http://ozone.univ-reims.fr and http://ozone.iao.ru .
  6. C. Jansen, J. Guenther, K. Mauersberger, D. Krankowsky, “Kinetic origin of the ozone isotope effect: a critical analysis of enrichments and rate coefficients,” Phys. Chem. Chem. Phys. 3, 4718–4721 (2001).
    [CrossRef]
  7. J. J. Plateaux, A. Barbe, A. Delahaigue, “Reims high resolution F. T. S. data reduction for ozone,” Spectrochim. Acta A 51, 1153–1169 (1995).
    [CrossRef]
  8. L. Régalia, “Mesures à l’aide d’un spectromètre par transformation de Fourier, des intensités et coefficients d’élargissement de molécules d’intérêt atmosphérique. Etude des précisions: application à N2O, H2O, O3,” M. S. Thesis (Reims University, Reims, France, 1996).
  9. J. J. Plateaux, L. Régalia, C. Boussin, A. Barbe, “A multispectrum fitting technique for data recorded by Fourier Transform spectrometer,” J. Quant. Spectrosc. Radiat. Transfer 68, 507–520 (2001).
    [CrossRef]
  10. Vl. G. Tyuterev, S. A. Tashkun, D. Schwenke, A. Barbe, “Isotopically invariant potential function of the ozone molecule,” in Proceedings of Highrus Conference, Proc. SPIE (to be published).
  11. Vl. G. Tyuterev, T. Cours, S. A. Tashkun, P. Jensen, A. Barbe “Potential function of the ozone molecule: global calculations of the rovibrational states and the dissociation behaviour,” in the 13th Symposium and School on High-Resolution Molecular Spectroscopy,” L. N. Sinitsa, editor, Proc. SPIE4063, 142–151 (1999).
  12. R. Siebert, P. Fleurat-Lessard, R. Schinke, M. Bittererova, S. C. Farantos, “The vibrational energies of ozone up to the dissociation threshold: dynamics calculations on an accurate potential energy surface,” J. Chem. Phys. 116, 9749–9767 (2002).
    [CrossRef]
  13. C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
    [CrossRef]
  14. J. K. G. Watson, “Determination of centrifugal distortion coefficients of asymmetric top molecules,” J. Chem. Phys. 46, 4189–4196 (1967).
    [CrossRef]
  15. J. M. Flaud, R. Bacis, “The ozone molecule: infrared and microwave spectroscopy,” Spectrochim Acta Part A 54, 3–16 (1998).
    [CrossRef]
  16. V. I. Perevalov, Vl. G. Tyuterev, “Effective centrifugal distortion Hamiltonian with empirically determinable parameters in the case of Coriolis resonances for asymmetric top molecules,” Opt. Spectrosk. 52, 644–650 (1982).
  17. S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, A. Chichery, “High-resolution IR spectra of the ozone molecule,” Atmos. Oceanic Opt 12, 771–785 (1999).
  18. A. Chichery, A. Barbe, Vl. G. Tyuterev, M. T. Bourgeois, “Analysis of high resolution spectra of 18O3. 1-Spectral range 1300–3100 cm-1,” J. Mol. Spectrosc. 206, 1–13 (2001).
    [CrossRef] [PubMed]
  19. A. Chichery, A. Barbe, Vl. G. Tyuterev, “Analysis of high resolution spectra of 18O3. 2-Spectral range 3100–4900 cm-1,” J. Mol. Spectrosc. 206, 14–26 (2001).
    [CrossRef] [PubMed]
  20. S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, “Extended analysis of line positions and intensities of ozone bands in the 2900–3400 cm-1 region,” J. Mol. Spectrosc. 215, 29–41 (2002).
    [CrossRef]
  21. A. Barbe, “High resolution infrared spectroscopy of ozone: a support for atmospheric observations,” Computational Technologies 7, 12–23 (2002).
  22. J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
    [CrossRef]
  23. A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
    [CrossRef]
  24. M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
    [CrossRef]
  25. A. Chichery, A. Barbe, VI. G. Tyuterev, S. Tashkun, “High resolution IR spectra of 18O enriched ozone: band centers of 16O16O18O, 16O18O18O, 18O16O18O and 16O18O16O,” J. Mol. Spectrosc. 205, 347–349 (2001).
    [CrossRef] [PubMed]

2003 (1)

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “Infrared spectrum of 16O18O16O in the 5μm range. Positions, intensities and atmospheric applications,” Atm. Optics Ocean, 16, 206–211 (2003).

2002 (5)

M. R. De Backer-Barilly, A. Barbe, S. A. Tashkun, Vl. G. Tyuterev, A. Chichery, “The 5ν3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O,” Mol. Phys. 22, 3499–3506 (2002).
[CrossRef]

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, A. Chichery, M. T. Bourgeois, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1 lines positions,” J. Mol. Spectrosc. 216, 454–464 (2002).
[CrossRef]

R. Siebert, P. Fleurat-Lessard, R. Schinke, M. Bittererova, S. C. Farantos, “The vibrational energies of ozone up to the dissociation threshold: dynamics calculations on an accurate potential energy surface,” J. Chem. Phys. 116, 9749–9767 (2002).
[CrossRef]

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, “Extended analysis of line positions and intensities of ozone bands in the 2900–3400 cm-1 region,” J. Mol. Spectrosc. 215, 29–41 (2002).
[CrossRef]

A. Barbe, “High resolution infrared spectroscopy of ozone: a support for atmospheric observations,” Computational Technologies 7, 12–23 (2002).

2001 (5)

A. Chichery, A. Barbe, Vl. G. Tyuterev, M. T. Bourgeois, “Analysis of high resolution spectra of 18O3. 1-Spectral range 1300–3100 cm-1,” J. Mol. Spectrosc. 206, 1–13 (2001).
[CrossRef] [PubMed]

A. Chichery, A. Barbe, Vl. G. Tyuterev, “Analysis of high resolution spectra of 18O3. 2-Spectral range 3100–4900 cm-1,” J. Mol. Spectrosc. 206, 14–26 (2001).
[CrossRef] [PubMed]

J. J. Plateaux, L. Régalia, C. Boussin, A. Barbe, “A multispectrum fitting technique for data recorded by Fourier Transform spectrometer,” J. Quant. Spectrosc. Radiat. Transfer 68, 507–520 (2001).
[CrossRef]

C. Jansen, J. Guenther, K. Mauersberger, D. Krankowsky, “Kinetic origin of the ozone isotope effect: a critical analysis of enrichments and rate coefficients,” Phys. Chem. Chem. Phys. 3, 4718–4721 (2001).
[CrossRef]

A. Chichery, A. Barbe, VI. G. Tyuterev, S. Tashkun, “High resolution IR spectra of 18O enriched ozone: band centers of 16O16O18O, 16O18O18O, 18O16O18O and 16O18O16O,” J. Mol. Spectrosc. 205, 347–349 (2001).
[CrossRef] [PubMed]

1999 (1)

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, A. Chichery, “High-resolution IR spectra of the ozone molecule,” Atmos. Oceanic Opt 12, 771–785 (1999).

1998 (1)

J. M. Flaud, R. Bacis, “The ozone molecule: infrared and microwave spectroscopy,” Spectrochim Acta Part A 54, 3–16 (1998).
[CrossRef]

1995 (2)

J. J. Plateaux, A. Barbe, A. Delahaigue, “Reims high resolution F. T. S. data reduction for ozone,” Spectrochim. Acta A 51, 1153–1169 (1995).
[CrossRef]

M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
[CrossRef]

1990 (1)

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

1989 (1)

J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
[CrossRef]

1986 (1)

C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
[CrossRef]

1982 (1)

V. I. Perevalov, Vl. G. Tyuterev, “Effective centrifugal distortion Hamiltonian with empirically determinable parameters in the case of Coriolis resonances for asymmetric top molecules,” Opt. Spectrosk. 52, 644–650 (1982).

1967 (1)

J. K. G. Watson, “Determination of centrifugal distortion coefficients of asymmetric top molecules,” J. Chem. Phys. 46, 4189–4196 (1967).
[CrossRef]

Bacis, R.

J. M. Flaud, R. Bacis, “The ozone molecule: infrared and microwave spectroscopy,” Spectrochim Acta Part A 54, 3–16 (1998).
[CrossRef]

Barbe, A.

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “Infrared spectrum of 16O18O16O in the 5μm range. Positions, intensities and atmospheric applications,” Atm. Optics Ocean, 16, 206–211 (2003).

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, A. Chichery, M. T. Bourgeois, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1 lines positions,” J. Mol. Spectrosc. 216, 454–464 (2002).
[CrossRef]

M. R. De Backer-Barilly, A. Barbe, S. A. Tashkun, Vl. G. Tyuterev, A. Chichery, “The 5ν3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O,” Mol. Phys. 22, 3499–3506 (2002).
[CrossRef]

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, “Extended analysis of line positions and intensities of ozone bands in the 2900–3400 cm-1 region,” J. Mol. Spectrosc. 215, 29–41 (2002).
[CrossRef]

A. Barbe, “High resolution infrared spectroscopy of ozone: a support for atmospheric observations,” Computational Technologies 7, 12–23 (2002).

A. Chichery, A. Barbe, Vl. G. Tyuterev, “Analysis of high resolution spectra of 18O3. 2-Spectral range 3100–4900 cm-1,” J. Mol. Spectrosc. 206, 14–26 (2001).
[CrossRef] [PubMed]

A. Chichery, A. Barbe, Vl. G. Tyuterev, M. T. Bourgeois, “Analysis of high resolution spectra of 18O3. 1-Spectral range 1300–3100 cm-1,” J. Mol. Spectrosc. 206, 1–13 (2001).
[CrossRef] [PubMed]

J. J. Plateaux, L. Régalia, C. Boussin, A. Barbe, “A multispectrum fitting technique for data recorded by Fourier Transform spectrometer,” J. Quant. Spectrosc. Radiat. Transfer 68, 507–520 (2001).
[CrossRef]

A. Chichery, A. Barbe, VI. G. Tyuterev, S. Tashkun, “High resolution IR spectra of 18O enriched ozone: band centers of 16O16O18O, 16O18O18O, 18O16O18O and 16O18O16O,” J. Mol. Spectrosc. 205, 347–349 (2001).
[CrossRef] [PubMed]

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, A. Chichery, “High-resolution IR spectra of the ozone molecule,” Atmos. Oceanic Opt 12, 771–785 (1999).

J. J. Plateaux, A. Barbe, A. Delahaigue, “Reims high resolution F. T. S. data reduction for ozone,” Spectrochim. Acta A 51, 1153–1169 (1995).
[CrossRef]

M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
[CrossRef]

Vl. G. Tyuterev, S. A. Tashkun, D. Schwenke, A. Barbe, “Isotopically invariant potential function of the ozone molecule,” in Proceedings of Highrus Conference, Proc. SPIE (to be published).

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1. Line positions,” J. Mol. Spectrosc. (2003), in press.

Vl. G. Tyuterev, T. Cours, S. A. Tashkun, P. Jensen, A. Barbe “Potential function of the ozone molecule: global calculations of the rovibrational states and the dissociation behaviour,” in the 13th Symposium and School on High-Resolution Molecular Spectroscopy,” L. N. Sinitsa, editor, Proc. SPIE4063, 142–151 (1999).

Bittererova, M.

R. Siebert, P. Fleurat-Lessard, R. Schinke, M. Bittererova, S. C. Farantos, “The vibrational energies of ozone up to the dissociation threshold: dynamics calculations on an accurate potential energy surface,” J. Chem. Phys. 116, 9749–9767 (2002).
[CrossRef]

Bourgeois, M. T.

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, A. Chichery, M. T. Bourgeois, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1 lines positions,” J. Mol. Spectrosc. 216, 454–464 (2002).
[CrossRef]

A. Chichery, A. Barbe, Vl. G. Tyuterev, M. T. Bourgeois, “Analysis of high resolution spectra of 18O3. 1-Spectral range 1300–3100 cm-1,” J. Mol. Spectrosc. 206, 1–13 (2001).
[CrossRef] [PubMed]

M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
[CrossRef]

Boussin, C.

J. J. Plateaux, L. Régalia, C. Boussin, A. Barbe, “A multispectrum fitting technique for data recorded by Fourier Transform spectrometer,” J. Quant. Spectrosc. Radiat. Transfer 68, 507–520 (2001).
[CrossRef]

Camy-Peyret, C.

M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
[CrossRef]

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
[CrossRef]

C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
[CrossRef]

Chichery, A.

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, A. Chichery, M. T. Bourgeois, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1 lines positions,” J. Mol. Spectrosc. 216, 454–464 (2002).
[CrossRef]

M. R. De Backer-Barilly, A. Barbe, S. A. Tashkun, Vl. G. Tyuterev, A. Chichery, “The 5ν3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O,” Mol. Phys. 22, 3499–3506 (2002).
[CrossRef]

A. Chichery, A. Barbe, Vl. G. Tyuterev, “Analysis of high resolution spectra of 18O3. 2-Spectral range 3100–4900 cm-1,” J. Mol. Spectrosc. 206, 14–26 (2001).
[CrossRef] [PubMed]

A. Chichery, A. Barbe, Vl. G. Tyuterev, M. T. Bourgeois, “Analysis of high resolution spectra of 18O3. 1-Spectral range 1300–3100 cm-1,” J. Mol. Spectrosc. 206, 1–13 (2001).
[CrossRef] [PubMed]

A. Chichery, A. Barbe, VI. G. Tyuterev, S. Tashkun, “High resolution IR spectra of 18O enriched ozone: band centers of 16O16O18O, 16O18O18O, 18O16O18O and 16O18O16O,” J. Mol. Spectrosc. 205, 347–349 (2001).
[CrossRef] [PubMed]

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, A. Chichery, “High-resolution IR spectra of the ozone molecule,” Atmos. Oceanic Opt 12, 771–785 (1999).

Cours, T.

Vl. G. Tyuterev, T. Cours, S. A. Tashkun, P. Jensen, A. Barbe “Potential function of the ozone molecule: global calculations of the rovibrational states and the dissociation behaviour,” in the 13th Symposium and School on High-Resolution Molecular Spectroscopy,” L. N. Sinitsa, editor, Proc. SPIE4063, 142–151 (1999).

De Backer-Barilly, M. R.

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “Infrared spectrum of 16O18O16O in the 5μm range. Positions, intensities and atmospheric applications,” Atm. Optics Ocean, 16, 206–211 (2003).

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, A. Chichery, M. T. Bourgeois, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1 lines positions,” J. Mol. Spectrosc. 216, 454–464 (2002).
[CrossRef]

M. R. De Backer-Barilly, A. Barbe, S. A. Tashkun, Vl. G. Tyuterev, A. Chichery, “The 5ν3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O,” Mol. Phys. 22, 3499–3506 (2002).
[CrossRef]

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1. Line positions,” J. Mol. Spectrosc. (2003), in press.

Delahaigue, A.

J. J. Plateaux, A. Barbe, A. Delahaigue, “Reims high resolution F. T. S. data reduction for ozone,” Spectrochim. Acta A 51, 1153–1169 (1995).
[CrossRef]

Farantos, S. C.

R. Siebert, P. Fleurat-Lessard, R. Schinke, M. Bittererova, S. C. Farantos, “The vibrational energies of ozone up to the dissociation threshold: dynamics calculations on an accurate potential energy surface,” J. Chem. Phys. 116, 9749–9767 (2002).
[CrossRef]

Flaud, J. M.

J. M. Flaud, R. Bacis, “The ozone molecule: infrared and microwave spectroscopy,” Spectrochim Acta Part A 54, 3–16 (1998).
[CrossRef]

M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
[CrossRef]

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
[CrossRef]

C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
[CrossRef]

Fleurat-Lessard, P.

R. Siebert, P. Fleurat-Lessard, R. Schinke, M. Bittererova, S. C. Farantos, “The vibrational energies of ozone up to the dissociation threshold: dynamics calculations on an accurate potential energy surface,” J. Chem. Phys. 116, 9749–9767 (2002).
[CrossRef]

Guenther, J.

C. Jansen, J. Guenther, K. Mauersberger, D. Krankowsky, “Kinetic origin of the ozone isotope effect: a critical analysis of enrichments and rate coefficients,” Phys. Chem. Chem. Phys. 3, 4718–4721 (2001).
[CrossRef]

Jansen, C.

C. Jansen, J. Guenther, K. Mauersberger, D. Krankowsky, “Kinetic origin of the ozone isotope effect: a critical analysis of enrichments and rate coefficients,” Phys. Chem. Chem. Phys. 3, 4718–4721 (2001).
[CrossRef]

Jensen, P.

Vl. G. Tyuterev, T. Cours, S. A. Tashkun, P. Jensen, A. Barbe “Potential function of the ozone molecule: global calculations of the rovibrational states and the dissociation behaviour,” in the 13th Symposium and School on High-Resolution Molecular Spectroscopy,” L. N. Sinitsa, editor, Proc. SPIE4063, 142–151 (1999).

Krankowsky, D.

C. Jansen, J. Guenther, K. Mauersberger, D. Krankowsky, “Kinetic origin of the ozone isotope effect: a critical analysis of enrichments and rate coefficients,” Phys. Chem. Chem. Phys. 3, 4718–4721 (2001).
[CrossRef]

Malathy Devi, V.

C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
[CrossRef]

Malathy-Devi, V.

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
[CrossRef]

Mauersberger, K.

C. Jansen, J. Guenther, K. Mauersberger, D. Krankowsky, “Kinetic origin of the ozone isotope effect: a critical analysis of enrichments and rate coefficients,” Phys. Chem. Chem. Phys. 3, 4718–4721 (2001).
[CrossRef]

Mikhailenko, S.

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, “Extended analysis of line positions and intensities of ozone bands in the 2900–3400 cm-1 region,” J. Mol. Spectrosc. 215, 29–41 (2002).
[CrossRef]

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, A. Chichery, “High-resolution IR spectra of the ozone molecule,” Atmos. Oceanic Opt 12, 771–785 (1999).

N’Gom, A.

J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
[CrossRef]

Perevalov, V. I.

V. I. Perevalov, Vl. G. Tyuterev, “Effective centrifugal distortion Hamiltonian with empirically determinable parameters in the case of Coriolis resonances for asymmetric top molecules,” Opt. Spectrosk. 52, 644–650 (1982).

Perrin, A.

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
[CrossRef]

Plateaux,

M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
[CrossRef]

Plateaux, J. J.

J. J. Plateaux, L. Régalia, C. Boussin, A. Barbe, “A multispectrum fitting technique for data recorded by Fourier Transform spectrometer,” J. Quant. Spectrosc. Radiat. Transfer 68, 507–520 (2001).
[CrossRef]

J. J. Plateaux, A. Barbe, A. Delahaigue, “Reims high resolution F. T. S. data reduction for ozone,” Spectrochim. Acta A 51, 1153–1169 (1995).
[CrossRef]

Régalia, L.

J. J. Plateaux, L. Régalia, C. Boussin, A. Barbe, “A multispectrum fitting technique for data recorded by Fourier Transform spectrometer,” J. Quant. Spectrosc. Radiat. Transfer 68, 507–520 (2001).
[CrossRef]

M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
[CrossRef]

L. Régalia, “Mesures à l’aide d’un spectromètre par transformation de Fourier, des intensités et coefficients d’élargissement de molécules d’intérêt atmosphérique. Etude des précisions: application à N2O, H2O, O3,” M. S. Thesis (Reims University, Reims, France, 1996).

Rinsland, C. P.

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
[CrossRef]

C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
[CrossRef]

Schinke, R.

R. Siebert, P. Fleurat-Lessard, R. Schinke, M. Bittererova, S. C. Farantos, “The vibrational energies of ozone up to the dissociation threshold: dynamics calculations on an accurate potential energy surface,” J. Chem. Phys. 116, 9749–9767 (2002).
[CrossRef]

Schwenke, D.

Vl. G. Tyuterev, S. A. Tashkun, D. Schwenke, A. Barbe, “Isotopically invariant potential function of the ozone molecule,” in Proceedings of Highrus Conference, Proc. SPIE (to be published).

Siebert, R.

R. Siebert, P. Fleurat-Lessard, R. Schinke, M. Bittererova, S. C. Farantos, “The vibrational energies of ozone up to the dissociation threshold: dynamics calculations on an accurate potential energy surface,” J. Chem. Phys. 116, 9749–9767 (2002).
[CrossRef]

Smith, M. A. H.

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
[CrossRef]

C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
[CrossRef]

Tashkun, S.

A. Chichery, A. Barbe, VI. G. Tyuterev, S. Tashkun, “High resolution IR spectra of 18O enriched ozone: band centers of 16O16O18O, 16O18O18O, 18O16O18O and 16O18O16O,” J. Mol. Spectrosc. 205, 347–349 (2001).
[CrossRef] [PubMed]

Tashkun, S. A.

M. R. De Backer-Barilly, A. Barbe, S. A. Tashkun, Vl. G. Tyuterev, A. Chichery, “The 5ν3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O,” Mol. Phys. 22, 3499–3506 (2002).
[CrossRef]

Vl. G. Tyuterev, T. Cours, S. A. Tashkun, P. Jensen, A. Barbe “Potential function of the ozone molecule: global calculations of the rovibrational states and the dissociation behaviour,” in the 13th Symposium and School on High-Resolution Molecular Spectroscopy,” L. N. Sinitsa, editor, Proc. SPIE4063, 142–151 (1999).

Vl. G. Tyuterev, S. A. Tashkun, D. Schwenke, A. Barbe, “Isotopically invariant potential function of the ozone molecule,” in Proceedings of Highrus Conference, Proc. SPIE (to be published).

Tyuterev, VI. G.

A. Chichery, A. Barbe, VI. G. Tyuterev, S. Tashkun, “High resolution IR spectra of 18O enriched ozone: band centers of 16O16O18O, 16O18O18O, 18O16O18O and 16O18O16O,” J. Mol. Spectrosc. 205, 347–349 (2001).
[CrossRef] [PubMed]

Tyuterev, Vl. G.

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “Infrared spectrum of 16O18O16O in the 5μm range. Positions, intensities and atmospheric applications,” Atm. Optics Ocean, 16, 206–211 (2003).

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, A. Chichery, M. T. Bourgeois, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1 lines positions,” J. Mol. Spectrosc. 216, 454–464 (2002).
[CrossRef]

M. R. De Backer-Barilly, A. Barbe, S. A. Tashkun, Vl. G. Tyuterev, A. Chichery, “The 5ν3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O,” Mol. Phys. 22, 3499–3506 (2002).
[CrossRef]

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, “Extended analysis of line positions and intensities of ozone bands in the 2900–3400 cm-1 region,” J. Mol. Spectrosc. 215, 29–41 (2002).
[CrossRef]

A. Chichery, A. Barbe, Vl. G. Tyuterev, “Analysis of high resolution spectra of 18O3. 2-Spectral range 3100–4900 cm-1,” J. Mol. Spectrosc. 206, 14–26 (2001).
[CrossRef] [PubMed]

A. Chichery, A. Barbe, Vl. G. Tyuterev, M. T. Bourgeois, “Analysis of high resolution spectra of 18O3. 1-Spectral range 1300–3100 cm-1,” J. Mol. Spectrosc. 206, 1–13 (2001).
[CrossRef] [PubMed]

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, A. Chichery, “High-resolution IR spectra of the ozone molecule,” Atmos. Oceanic Opt 12, 771–785 (1999).

V. I. Perevalov, Vl. G. Tyuterev, “Effective centrifugal distortion Hamiltonian with empirically determinable parameters in the case of Coriolis resonances for asymmetric top molecules,” Opt. Spectrosk. 52, 644–650 (1982).

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1. Line positions,” J. Mol. Spectrosc. (2003), in press.

Vl. G. Tyuterev, S. A. Tashkun, D. Schwenke, A. Barbe, “Isotopically invariant potential function of the ozone molecule,” in Proceedings of Highrus Conference, Proc. SPIE (to be published).

Vl. G. Tyuterev, T. Cours, S. A. Tashkun, P. Jensen, A. Barbe “Potential function of the ozone molecule: global calculations of the rovibrational states and the dissociation behaviour,” in the 13th Symposium and School on High-Resolution Molecular Spectroscopy,” L. N. Sinitsa, editor, Proc. SPIE4063, 142–151 (1999).

Vasserot, A. M.

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

Watson, J. K. G.

J. K. G. Watson, “Determination of centrifugal distortion coefficients of asymmetric top molecules,” J. Chem. Phys. 46, 4189–4196 (1967).
[CrossRef]

Atm. Optics Ocean (1)

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “Infrared spectrum of 16O18O16O in the 5μm range. Positions, intensities and atmospheric applications,” Atm. Optics Ocean, 16, 206–211 (2003).

Atmos. Oceanic Opt (1)

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, A. Chichery, “High-resolution IR spectra of the ozone molecule,” Atmos. Oceanic Opt 12, 771–785 (1999).

Computational Technologies (1)

A. Barbe, “High resolution infrared spectroscopy of ozone: a support for atmospheric observations,” Computational Technologies 7, 12–23 (2002).

J. Chem. Phys. (2)

R. Siebert, P. Fleurat-Lessard, R. Schinke, M. Bittererova, S. C. Farantos, “The vibrational energies of ozone up to the dissociation threshold: dynamics calculations on an accurate potential energy surface,” J. Chem. Phys. 116, 9749–9767 (2002).
[CrossRef]

J. K. G. Watson, “Determination of centrifugal distortion coefficients of asymmetric top molecules,” J. Chem. Phys. 46, 4189–4196 (1967).
[CrossRef]

J. Mol. Spectrosc. (9)

C. Camy-Peyret, J. M. Flaud, A. Perrin, V. Malathy Devi, C. P. Rinsland, M. A. H. Smith, “The hybrid-type bands ν1 and ν3 of 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 118, 345–354 (1986).
[CrossRef]

A. Chichery, A. Barbe, Vl. G. Tyuterev, M. T. Bourgeois, “Analysis of high resolution spectra of 18O3. 1-Spectral range 1300–3100 cm-1,” J. Mol. Spectrosc. 206, 1–13 (2001).
[CrossRef] [PubMed]

A. Chichery, A. Barbe, Vl. G. Tyuterev, “Analysis of high resolution spectra of 18O3. 2-Spectral range 3100–4900 cm-1,” J. Mol. Spectrosc. 206, 14–26 (2001).
[CrossRef] [PubMed]

S. Mikhailenko, A. Barbe, Vl. G. Tyuterev, “Extended analysis of line positions and intensities of ozone bands in the 2900–3400 cm-1 region,” J. Mol. Spectrosc. 215, 29–41 (2002).
[CrossRef]

J. M. Flaud, C. Camy-Peyret, A. N’Gom, V. Malathy-Devi, C. P. Rinsland, M. A. H. Smith, “The ν2 bands of 16O18O16O and 16O16O18O: line positions and intensities,” J. Mol. Spectrosc. 133, 217–223 (1989).
[CrossRef]

A. Perrin, A. M. Vasserot, J. M. Flaud, C. Camy-Peyret, C. P. Rinsland, M. A. H. Smith, V. Malathy-Devi, “The ν2 bands of 18O3, 18O16O18O and 16O18O18O: line positions and intensities,” J. Mol. Spectrosc. 143, 311–317 (1990).
[CrossRef]

M. T. Bourgeois, J. M. Flaud, A. Barbe, L. Régalia, C. Camy-Peyret, Plateaux,” The ν1+ν3 bands of 16O18O18O and 18O16O18O,” J. Mol. Spectrosc. 172, 552–558 (1995).
[CrossRef]

A. Chichery, A. Barbe, VI. G. Tyuterev, S. Tashkun, “High resolution IR spectra of 18O enriched ozone: band centers of 16O16O18O, 16O18O18O, 18O16O18O and 16O18O16O,” J. Mol. Spectrosc. 205, 347–349 (2001).
[CrossRef] [PubMed]

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, A. Chichery, M. T. Bourgeois, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1 lines positions,” J. Mol. Spectrosc. 216, 454–464 (2002).
[CrossRef]

J. Quant. Spectrosc. Radiat. Transfer (1)

J. J. Plateaux, L. Régalia, C. Boussin, A. Barbe, “A multispectrum fitting technique for data recorded by Fourier Transform spectrometer,” J. Quant. Spectrosc. Radiat. Transfer 68, 507–520 (2001).
[CrossRef]

Mol. Phys. (1)

M. R. De Backer-Barilly, A. Barbe, S. A. Tashkun, Vl. G. Tyuterev, A. Chichery, “The 5ν3 bands of 18O enriched ozone: line positions of 16O16O18O, 16O18O16O, 16O18O18O and 18O16O18O,” Mol. Phys. 22, 3499–3506 (2002).
[CrossRef]

Opt. Spectrosk. (1)

V. I. Perevalov, Vl. G. Tyuterev, “Effective centrifugal distortion Hamiltonian with empirically determinable parameters in the case of Coriolis resonances for asymmetric top molecules,” Opt. Spectrosk. 52, 644–650 (1982).

Phys. Chem. Chem. Phys. (1)

C. Jansen, J. Guenther, K. Mauersberger, D. Krankowsky, “Kinetic origin of the ozone isotope effect: a critical analysis of enrichments and rate coefficients,” Phys. Chem. Chem. Phys. 3, 4718–4721 (2001).
[CrossRef]

Spectrochim Acta Part A (1)

J. M. Flaud, R. Bacis, “The ozone molecule: infrared and microwave spectroscopy,” Spectrochim Acta Part A 54, 3–16 (1998).
[CrossRef]

Spectrochim. Acta A (1)

J. J. Plateaux, A. Barbe, A. Delahaigue, “Reims high resolution F. T. S. data reduction for ozone,” Spectrochim. Acta A 51, 1153–1169 (1995).
[CrossRef]

Other (5)

L. Régalia, “Mesures à l’aide d’un spectromètre par transformation de Fourier, des intensités et coefficients d’élargissement de molécules d’intérêt atmosphérique. Etude des précisions: application à N2O, H2O, O3,” M. S. Thesis (Reims University, Reims, France, 1996).

Vl. G. Tyuterev, S. A. Tashkun, D. Schwenke, A. Barbe, “Isotopically invariant potential function of the ozone molecule,” in Proceedings of Highrus Conference, Proc. SPIE (to be published).

Vl. G. Tyuterev, T. Cours, S. A. Tashkun, P. Jensen, A. Barbe “Potential function of the ozone molecule: global calculations of the rovibrational states and the dissociation behaviour,” in the 13th Symposium and School on High-Resolution Molecular Spectroscopy,” L. N. Sinitsa, editor, Proc. SPIE4063, 142–151 (1999).

M. R. De Backer-Barilly, A. Barbe, Vl. G. Tyuterev, “High resolution infrared spectra of the 16O18O16O ozone isotopomer in the range 900–5000 cm-1. Line positions,” J. Mol. Spectrosc. (2003), in press.

Vl. G. Tyuterev, A. Barbe, S. N. Mikhailenko, Y. Babykov, “Spectroscopy and molecular properties of ozone,” http://ozone.univ-reims.fr and http://ozone.iao.ru .

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Figures (1)

Fig. 1
Fig. 1

Observed spectrum in the 5-μm spectral region.

Tables (3)

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Table 1 Pressures of the Two 16O-18O Ozone Mixtures

Tables Icon

Table 2 16O16O18O Observed Band Centers

Tables Icon

Table 3 18O18O16O Observed Band Centers

Equations (4)

Equations on this page are rendered with MathJax. Learn more.

V|H|V=EVV+A-12B+CJz2+12B+CJ2+12B-CJxy2-ΔKJz4-ΔJKJz2J2-ΔJJ22-δKJz2, Jxy2-2δJJxy2J2+HKJz6+HKJJz4J2+HJKJz2J22+HJJ23+hKJz4, Jxy2+hKJJz2, Jxy2J2+2hJJxy2J22,
V|H|V=V|HCoriolis|V+V|HAnharmonic|V
V|HCoriolis|V= C001J+-J-+C011J+Jz+½+Jz+½J- +C021J+Jz+½2-Jz+½2J- +C201J2J+-J- +C003J+3-J-3 +C031J+Jz+½3+Jz+½3J- +C211J2J+Jz+½+Jz+½J-+
V|HAnharmonic|V=F000+F200J2+F020Jz2+F002J+2+J-2+

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