IVR of Van der Waals and Hydrogen-Bonded Complexes as Studied by Stimulated Emission Ion Dip Spectroscopy

  • Mitsuo Ito
  • Toshinori Suzuki
  • Mikako Furukawa
  • Takayuki Ebata
Part of the NATO ASI Series book series (NSSB, volume 227)


Intramolecular vibrational redistribution (IVR) is an important nonradiative process in an isolated large molecule, and it is being extensively studied experimentally and theoretically. Especially, IVR in electronically excited state has been studied by various experimental means such as fluorescence excitation, dispersed fluorescence spectro-scopies and the measurement, of fluorescence life-time.1 As a result, our information on IVR for electronically excited states is now considerably accumulated. On the other hand, the study on IVR in electronically ground-state is very few. This is due to lack of suitable experimental means. The study by infrared radiation is an orthodox way. However, because of poor time response of the infrared detection and of severe selection rule for infrared absorption, the IVR study of a ground state molecule by infrared light is greatly restricted. Instead of direct vibrational excitation by infrared light, the ground-state vibrational level of an isolated nolecule can be populated by stimulated emission from an electronically excited state, say, S1 state with UV/visible laser light (v2). One of the stimulated emission methods is “stimulated emission pumping” in which the stimulated emission from S1 to a ground-state vibrational level is monitored by the dip of the fluorescence from the S1 level pumped with vl2–3 The depth of the fluorescence dip represents the decrease of the S1 state population which is determined by the balance of loss of the S1 state population by the stimulated emission with v2 and the gain of the population by the reabsorption with same v2 from the ground-state vibrational level. When the life-time of the ground-state vibrational level to which the stimulated emission occurs is long, the molecules in the vibrational level have a great chance to come back to S1, resulting in a small fluorescence dip. Conversely, when the life-time (decay rate) is short (large), we have a large dip. Since the lifetime of the ground-state vibrational level of an isolated molecule is in most cases determined by IVR process, we can obtain the IVR rate from the observed depth of the fluorescence dip. Therefore, the depth of the fluorescence dip measured in percentage relative to the fluorescence signal in absence of the stimulated emission provides us with very useful information on the IVR rate of ground-state vibrational level. However, the quantitative determination of the percentage fluorescence dip depth is very difficult because it requires complete spatial matching of the two laser beams v1 and v2. The observed percentage dip depth sensitively varies by mismatching of the two beams whose elimination is practically impossible.


Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.


  1. 1.
    See for example, (a) C. S. Parmenter, J. Phys. Chem. 86, 1736 (1982)Google Scholar
  2. (b).
    R. E. Smalley, J. Phys. Chem. 86, 3504 (1982)CrossRefGoogle Scholar
  3. (c).
    R.. E. Smalley, Ann. Rev. Phys. Chem. 34, 129 (1983).CrossRefGoogle Scholar
  4. 2.
    C. E. Hamilton, J. L. Kinsey and R. W. Field, Ann. Rev. Phys. Chem. 37, 493 (1986).ADSCrossRefGoogle Scholar
  5. 3.
    H. L. Kim, S. Reid and J. D. McDonald, Chem. Phys. Lett. 132, 361 (1986).CrossRefGoogle Scholar
  6. 4.
    T. Suzuki, N. Mikami and M. Ito, Chem. Phys. Lett. 120, 333 (1985).ADSCrossRefGoogle Scholar
  7. 5.
    T. Suzuki, N. Mikami and M. Ito, J. Phys. Chem. 90, 6431 (1986).CrossRefGoogle Scholar
  8. 6.
    T. Suzuki, M. Hiroi and M. Ito, J. Phys. Chem. 92, 3774 (1988).CrossRefGoogle Scholar
  9. 7.
    H. Abe, N. Mikami and M. Ito, J. Phys. Chem. 86, 1768 (1982).CrossRefGoogle Scholar
  10. 8.
    R. J. Lipert, G. Bermudez and S. D. Colson, J. Phys. Chem. 92, 3801 (1988).CrossRefGoogle Scholar
  11. 9.
    K. Okuyama, N. Mikami and M. Ito, J. Phys. Chem. 89, 5617 (1985).CrossRefGoogle Scholar

Copyright information

© Plenum Press, New York 1990

Authors and Affiliations

  • Mitsuo Ito
    • 1
  • Toshinori Suzuki
    • 1
  • Mikako Furukawa
    • 1
  • Takayuki Ebata
    • 1
  1. 1.Department of Chemistry Faculty of ScienceTohoku UniversitySendai 980Japan

Personalised recommendations