Excitonic interactions in conjugated chains are studied by analysing t
he optical and vibrational properties of unsubstituted thiophene oligo
mers with different supramolecular organization. Single quasi-planar m
olecules, electronically decoupled in the solid state, have been obtai
ned by inclusion of the thiophene oligomers in perhydrotriphenylene. R
esonant Raman scattering shows that the strong spectral changes which
occur upon molecular aggregation can be explained only by electronic e
xcited state interactions, in rather good agreement with the predictio
n of the molecular exciton model.