Effects of electronic delocalization on intramolecular proton transfer

The effects of molecular size, conjugation length, and competition with excimer formation on excited state intramolecular proton transfer (ESIPT) in conjugated polymers, in which the intramolecularly hydrogen-bonded moieties reside in the main chain, were examined. A large extent of π-electron delocalization is found to inhibit the ESIPT process. Excimer formation is found to be competitive with ESIPT in the polymers studied, whereas molecular size does not inhibit ESIPT.