Abstract
The considerable potential of high resolution time‐resolved spectroscopic data for copolymer systems in elucidation of the intramolecular photophysical processes which occur in polymer systems is illustrated. Such information can not be gleaned solely from studies of homopolymers. Kinetic data and time resolved fluorescence spectra of copolymers of 1‐vinylnaphthalene and methyl methacrylate indicate that conventional kinetic schemes are inappropriate for the discription of excimer formation in 1‐vinylnaphthalene polymers. Evidence is presented for the presence of an emitting species in addition to the expected monomeric and excimeric forms. The nature of this third species is discussed and photophysical kinetic schemes are proposed to describe intramolecular excimer formation in such systems. Kinetic data have been derived for the principle deactivation pathways through investigation of the observed fluorescence decays upon the intrachain concentration of aromatic species.