RADIATIONALESS DEACTIVATION OF TRIPLET CORONENE IN PLASTICS.

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1967

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Ohio State University

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A method has been developed using the intensities of delayed fluorescence and of phosphorescence of coronene which permits calculation of the rate constant for crossing to S1 from isoenergetic triplet levels (k61) as well as the S1T1 gap. For these calculations, measurements of the fluorescence yield, and the temperature dependence of both the phosphorescence lifetime and the ratio of delayed fluorescence to phosphorescence were made using polymethylmethaerylate specimens containing coronene-h12 and coronene-d12. The calculated S1T1 gap of 3930cm−1 agrees with the value obtained from the 0.0 bands of the fluorescence and phosphorescence spectra. Values of k61 of coronene-d12 and coronene-d12 are equal to within the experimental error and are significantly smaller than rate constant k3 for the reverse intersystem crossing from S1 to T1. The delayed fluorescence accounts for only a small fraction of the total radiationless deactivation of triplet coronene. The temperature-dependent part of the rate constant for deactivation of triplet coronene is larger for ordinary coronene than for deuterated coronene and is nearly the same for coronene-h12 in both polymethylmethaerylate and an epoxy resin, DER-332. These results are discussed in terms of possible mechanisms for temperature dependent deactivation of triplet coronene.

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Author Institution: TRW Systems Building R-1,

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