The preparation of polystyrene with controlled molar masses and narrow
dispersity endcapped with an anthrylmethyl ether group, as well as th
e study of their photophysical properties, are described. Under irradi
ation at 336 nm dimerisation of the polystyrene chains is observed. Th
is process results from the formation of a symmetrical head-to-tail ph
otodimer between two anthryl end groups. When irradiated at lower wave
length (lambda = 228 nm), the original omega-anthrylpolystyrene chains
are quantitatively restored. These dimerisation/dissociation cycles c
an be conducted more than ten times without any detectable degradation
of the photosensitive polymer. The fluorescence emission quantum yiel
d and fluorescence lifetime of the omega-anthryl moieties and the quan
tum yield of the dimerisation and of the reverse process have been mea
sured.