Block-copolymers of styrene and vinylpyridine are microheterogeneous m
edia where a separation occurs between the polar and the nonpolar phas
es. The aim of our work was to encage zinc porphyrin chromophores in t
he hydrophobic part of a polymer, polystyrene- block-poly(vinyl-2-pyri
dine), in order to obtain a model of charge separation in energy trans
fer. For this purpose, various porphyrins were attached to preformed p
olystyrene using two different methods: the Friedel-Crafts reaction be
tween polystyrene and porphyrins monofunctionalized by an acid chlorid
e and the Williamson reaction starting from polystyrene-co-poly(vinyl-
4-benzylchloride) and porphyrin monofunctionalized by a phenol substit
uent. The amount of grafted porphyrins was evaluated by visible and NM
R spectra and elemental analysis. The grafted porphyrins were then coe
vaporated with the block-copolymers to obtain thin films. The location
of the porphyrins was determined by electron microscopy and fluoresce
nce spectra. The results proved that the process is successful and the
se supported materials are under further investigation.