Abstract
Triple exciplex formed between polyacenaphthalene and terephthalic dimethylester (TDE) has been studied by means of the steady-state and time-resolved fluorescence spectra. The theoretical model of the triple exciplex formation for a flexible polymer chain in a dilute solution has been proposed. The fluorescence decays of the monomer, the exciplex and the triple exciplex obey a double exponential rule in the pbotophysical processes of the triple exciplex formation. The association rate constant of the exciplex formation is k_3=6.0×10~9s~(-1)(mol/L)~(-1); the association rate constant of the triple exciplex formation is k_6=5.2×10~7s~(-1). A mechanism for the triple exciplex formation from the exciplex to the triple exciplex has been proved through the noncrystal films corresponding to the same concentrations of the solution systems and the fluorescence lifetimes of the intramolecular excimer.
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