The excited state properties of many oligomers or polymers are of particula
r importance as they are directly related to light absorption and emission
as well as to photoconductivity, which govern most of their potential appli
cations. Oligomers with a finite, well-defined chain length can serve as mo
del systems for the investigation of general and fundamental properties of
the whole material class. We show that the primary gap excitations in a num
ber of such model systems are essentially delocalized over the entire molec
ules. The extension of the corresponding exciton scales with the molecule l
ength only and is fully independent of the details of the corresponding mol
ecular structure. (C) 2000 Elsevier Science B.V. All rights reserved.