Journal of Chemical Physics
Feedback | Help | Exit
The Journal of Chemical Physics
Search:
   
 
 
 
Previous Article
Fluorescence-dip infrared spectroscopy of tropolone and tropolone-OD
Fluorescence-dip infrared spectroscopy (FDIRS) is employed to record the infrared spectra of the isolated, jet-cooled tropolone molecule (TrOH) and its singly deuterated isotopomer TrOD in the O–...
Next Article
Infrared spectroscopy of OH stretching vibrations of hydrogen-bonded tropolone-(H2O)n (n=1–3) and tropolone-(CH3OH)n (n=1 and 2) clusters
Infrared spectra of jet-cooled tropolone-(H2O)n (n=1–3) and tropolone-(CH3OH)n (n=1 and 2) clusters were observed in the OH stretching region by using infrared-ultraviolet double resonance techni...

Fluorescence-dip infrared spectroscopy of the tropolone-H2O complex

J. Chem. Phys. 105, 2605 (1996); doi:10.1063/1.472125

Issue Date: 15 August 1996

You are not logged in to this journal. Log in

Rex K. Frost, Fredrick C. Hagemeister, Caleb A. Arrington, David Schleppenbach, and Timothy S. Zwier
Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-1393

Kenneth D. Jordan
Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260
Fluorescence dip infrared spectroscopy (FDIRS) is used to probe the effect of a solvent water molecule on intramolecular H-atom tunneling in tropolone. As with the bare molecule discussed in paper I, the FDIR spectrum of the tropolone-H2O complex is recorded in the O–H and C–H stretch regions. Three OH stretch fundamentals are observed in the spectrum, and can be assigned nominally to a free OH stretch of the water molecule (3724 cm–1), a hydrogen bonded OH stretch of water (3506 cm–1), and the OH stretch of tropolone (~3150 cm–1). The breadth and complexity of the bands is highly mode specific. The free OH stretch transition is sharp (1.8 cm–1 FWHM) and has weak combination bands built on it at +73 and +1600 cm–1. The former is assigned to a combination band with the in-plane bending mode of the tropolone-H2O hydrogen bond, while the latter is the free OH/intramolecular water bend combination band. The water hydrogen-bonded OH fundamental is also a sharp transition which, after correction for the decreased infrared power at its frequency, is clearly the strongest transition in the spectrum. It is flanked by three close-lying satellite bands 13, 23, and 34 cm–1 above it, and also supports a weak combination band at +69 cm–1 due to the in-plane intermolecular bending mode. The tropolone OH absorption is in the same frequency region as in the bare molecule, but broadened to over 100 cm–1 in TrOH–H2O. Distinct substructure in the band is present, with spacings reminiscent of those in the water H-bonded OH stretch region. Ab initio calculations on tropolone-H2O are carried out at both the MP2 and Becke3LYP levels of theory. Two isomers with similar binding energies and vibrational frequencies are identified. In one isomer (isomer I), the water molecule serves as a hydrogen-bonded bridge between the tropolone OH and keto groups. In the other (isomer II), the water molecule is exterior to the tropolone and hydrogen bonded to the keto oxygen. The experimental evidence does not conclusively distinguish between these two possibilities, though the exterior structure seems somewhat more in keeping with the data as a whole. ©1996 American Institute of Physics.
History: Received 13 March 1996; accepted 7 May 1996
Permalink: http://link.aip.org/link/?JCPSA6/105/2605/1
BUY THIS ARTICLE   (US$24)
Download PDF (227 kB) View Cart

KEYWORDS and PACS

Keywords
PACS
  • 33.20.Ea
    Molecular properties and interactions with photons Molecular spectra Infrared spectra
  • 33.50.Dq
    Molecular properties and interactions with photons Fluorescence and phosphorescence; radiationless transitions, quenching (intersystem crossing, internal conversion) Fluorescence and phosphorescence spectra
  • 31.70.Dk
    Electronic structure of atoms, molecules and their ions: theory Effects of atomic and molecular interactions on electronic structure Environmental and solvent effects
  • YEAR: 1996

RELATED DATABASES


To view database links for this article,
you need to log in.
To view database links for this article,
you need to log in.

PUBLICATION DATA

ISSN:
0021-9606 (print)   1089-7690 (online)
Publisher:
AIP is a member of CrossRef AIP

REFERENCES (28)
View in Separate Window/Tab
For access to fully linked references, you need to log in. For access to fully linked references, you need to Log in.
  1. Y. Tomioka, M. Ito, and N. Mikami, J. Phys. Chem. 87, 4401 (1983).
  2. H. Sekiya, H. Hamabe, N. Nakano, H. Ujita, N. Nakano, and Y. Nishimura, Chem. Phys. Lett. (in press).
  3. A. Mitsuzuka, A. Fujii, T. Ebata, and N. Mikami, J. Chem. Phys. 105, 2618 (1996), following paper.
  4. R. L. Redington and C. W. Bock, J. Phys. Chem. 95, 10284 (1991).
  5. R. K. Frost, F. Hagemeister, C. A. Arrington, and T. S. Zwier, J. Chem. Phys. 105, 2595 (1996), preceding paper.
  6. F. A. Ensminger, J. Plassard, T. S. Zwier, and S. Hardinger, J. Chem. Phys. 99, 8341 (1993).
  7. F. A. Ensminger, J. Plassard, T. S. Zwier, and S. Hardinger, J. Chem. Phys. 102, 5246 (1995).
  8. Z. S. Huang and R. E. Miller, J. Chem. Phys. 91, 6613 (1989).
  9. F. Huisken, M. Kaloudis, and A. Kulcke, J. Chem. Phys. 104, 17 (1996).
  10. R. N. Pribble and T. S. Zwier, Science 265, 75–79 (1994).
  11. R. N. Pribble and T. S. Zwier, Faraday Discuss. 97, 229 (1994).
  12. T. S. Zwier, Annu. Rev. Phys. Chem. (1996), Vol. 47, p. 205.
  13. S. Djafari, G. Lembach, H.-D. Barth, and B. Brutschy, Z. Phys. Chem. (in press).
  14. T. Ebata, T. Watanabe, and N. Mikami, J. Phys. Chem. 99, 5761 (1995).
  15. GAUSSIAN 94, Revision A.1, M. J. Frisch, G. W. Trucks, H. B. Schlegel, P. M. W. Gill, B. G. Johnson, M. A. Robb, J. R. Cheeseman, T. A. Keith, G. A. Petersson, J. A. Montgomery, K. Raghavachari, M. A. Al-Laham, V. G. Zakrzewski, J. V. Ortiz, J. B. Foresman, J. Cioslowki, B. B. Stefanov, A. Nanayakkara, M. Challacombe, C. Y. Peng, P. Y. Ayala, W. Chen, M. W. Wong, J. L. Andres, E. S. Replogle, R. Gomperts, R. L. Martin, D. J. Fox, J. S. Binkley, D. J. Defrees, J. Baker, J. P. Stewart, M. Head-Gordon, C. Gonzalez, and J. A. Pople, Gaussian, Inc., Pittsburgh, PA, 1995.
  16. C. Möller, M. S. Plesset, Phys. Rev. 46, 618 (1934);
    17. R. J. Bartlett, Annu. Rev. Phys. Chem. 32, 359 (1981).
  17. (a) A. D. Becke, J. Chem. Phys. 98, 5648 (1993);
    18. (b) S. H. Vosko, L. Wilk, M. Nusir, Can. J. Phys. 58, 1200 (1980);
    (c) C. Lee, W. Yang, and R. G. Parr, Phys. Rev. B 37, 785 (1988).
  18. S. F. Boys, F. Bernardi, Mol. Phys. 19, 553 (1970).
  19. (a) K. Kim, K. D. Jordan, and T. S. Zwier, J. Am. Chem. Soc. 116, 11568 (1994);
    20. (b) S. Y. Fredericks, K. D. Jordan, and T. S. Zwier, J. Phys. Chem. (in press).
  20. D. Forney, M. E. Jacox, and W. E. Thompson, J. Mol. Spectrosc. 157, 479 (1993).
  21. E. F. Breheret and M. M. Martin, J. Lumin. 17, 49 (1978).
  22. (a) M. Pohl, M. Schmitt, K. Kleinermanns, J. Chem. Phys. 94, 1717 (1991);
    23. (b) V. Brenner, S. Martenchard-Barra, P. Millie, C. Dedonder-Lardeux, C. Jouvet, and D. Solgadi, J. Phys. Chem. 99, 5848 (1995).
  23. G. C. Pimentel and A. L. McClellan, The Hydrogen Bond (Freeman, San Francisco, 1960).
  24. H. Sekiya, Y. Nagashima, and Y. Nishimura, J. Chem. Phys. 92, 5761 (1990).
  25. R. L. Redington, Y. Chen, G. J. Scherer, and R. W. Field, J. Chem. Phys. 88, 627 (1988).
  26. (a) A. C. Legon and D. J. Millen, Chem. Rev. 86, 635 (1986), and references therein;
    27. (b) D. J. Millen, J. Mol. Struct. 100, 351 (1983).
  27. N. Sheppard, in Hydrogen Bonding, edited by D. Hadzi (Pergamon, New York, 1959), p. 85.
  28. R. N. Pribble, A. W. Garrett, K. Haber, and T. S. Zwier, J. Chem. Phys. 103, 531 (1995).

CITING ARTICLES
For access to citing articles, you need to log in.
For access to citing articles, you need to Log in.


Copyright © American Institute of Physics