Photoreactions of acrylic polymers containing pendant ethyl phenylglyo
xylate groups at different distances from the polymeric backbone have
been studied. Hydrogen abstraction between pendant groups by an excite
d triplet phenylglgoxylate carbonyl group from adjacent pendant groups
is the primary process. The expected gamma-hydrogen abstraction withi
n one pendant group (the Norrish type II reaction) is not observed. Th
e radicals formed react with each other to form cross-linked structure
s in the polymer. This effects solubility in various solvents which ch
anges significantly after irradiation. The potential of the polymer as
an imageable material has been evaluated.