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Picosecond photophysical processes in iodoanthracenes

Thesis/Dissertation ·
OSTI ID:5676355

Picosecond photophysical processes in 2- and 9-iodoanthracene in cyclohexane at room temperature were studied by triplet-triplet transient absorption spectroscopy between 420-500 nanometers. For small amounts of excess vibronic energy in S/sub 1/, intersystem crossing from the first excited singlet state into high triplet states T/sub n/ (n > 1) with subsequent internal conversion to T/sub 1/ or dissociation from the upper triplet manifold is suggested as a primary pathway for nonradiative relaxation. Rate constants for the processes were estimated using the results from previous fluorescence studies and the population risetime data for T/sub 1/. Analyses of the photoproducts generated by excitation at two different wavelengths into the first excited singlet state reveal a vibronic level dependence of the photodissociation yield, indicating that photodissociation can proceed via at least two different mechanisms in the iodoanthracenes. Stimulated Raman processes and self-action effects are shown to be primarily responsible for the generation of a picosecond continuum when 532 nm picosecond pulses are focused into a CCl/sub 4/ continuum cell. An experimental assessment of the artifacts introduced by the angular distribution of continuum light on the triplet-triplet absorption spectra of acridine is given and procedures to minimize these effects are suggested.

DOE Contract Number:
W-7405-ENG-82
OSTI ID:
5676355
Country of Publication:
United States
Language:
English

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