We present Raman studies on various substituted polyvinylcinnamates, [
-CH2CH(O2CCH=CHC6H5)-](n), are well known for undergoing cycloaddition
when exposed to UV radiation. Our comparative studies on these unphot
otransformed polymers show that the substitutions on the aryl cycle pl
ay a fundamental role in the vibrational dynamics of these molecules.
We have been able to identify the characteristic modes of each type of
fluoro-substitution (mono, para and ortho), and as a result, it is po
ssible to determine whether the two isomers and two rotating conformer
s coexist in the samples. In order to proceed to further investigation
s on the phototransformation process, we have determined how the C=C a
nd C=O double-bond stretching modes behave versus the type of substitu
tion. (C) 1998 Elsevier Science S.A. All rights reserved.