Abstract
The emission lifetimes of matrix‐stabilized dimers of anthracene and its derivatives were observed. The two principal conformations considered were the sandwich excimers and the 55° dimers. The excimer lifetimes may be of use in establishing wavefunctions for these transient states. A comparison of the lifetimes and emission structure from the dimers in rigid solvents with the time and wavelength structure of emission from strained crystals permits identification of a crystal defect in anthracene. The variable structure of anthracene thin films was demonstrated and partially identified.
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