KrF laser irradiation of thin films of poly(4-trimethylsilylmethylstyrene) (PTMSMS) under
atmospheric conditions induced oxygenation at the film surface and cross-linking inside the film. The
irradiated film surface became hydrophilic owing to the formation of carboxylic acid group, and the photo-cross-linking caused the insolubilization of the film inside. Similar irradiation of poly(4-methylstyrene)
(P4MS) and polystyrene (PS) films, on the other hand, induced oxidative degradation of the polymer
main chain. Selectivity in the bond cleavage involved in their photoreactions would lead to the contrast
results. Selective cleavage of the benzylic C−Si bond of PTMSMS gives benzyl-type radicals, which react
with oxygen, leading to the formation of carboxylic acid groups at the surface, or couple with each other,
giving the cross-linked structure inside the film. Cleavage of the C−H bond of the main chain in P4MS
and PS would be involved in the oxidative degradation of the polymer main chain. Since the cross-linking
is an apparent two-photon reaction and requires the closely formed radicals, efficiency of the C−Si bond
cleavage and the following radical formation at the 4-position of the benzene ring also must play a crucial
role in the cross-linking ability.