Direct Timing of the Relaxation from Selected Excited States; Beta-Naphthylamine

  • E. W. Schlag
    Department of Chemistry, Northwestern University, Evanston, Illinois 60201
  • H. v. Weyssenhoff
    Department of Chemistry, Illinois Institute of Technology, Chicago, Illinois

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<jats:p>The fluorescence of β-naphthylamine vapor in the low-pressure region was timed directly using a high-speed laboratory light modulator. Emission was from defined, and variable quantum states initially pumped with high-intensity monochromatic light. The energy of irradiation was swept over a range of 10 000 cm−1, encompassing two excited electronic manifolds. The results then constitute a direct timed measurement of the relaxation from individual vibronic states as the energy of excitation is continuously increased. This is then a spectrum of vibronic lifetimes which is discussed in terms of various theories for electronic relaxation.</jats:p>

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