S. Chmela et al., PHOTO-HYDROPEROXIDATION AND GRAFTING OF POLYOCTENAMER - ACCESS TO NEWPOLYMERIC-HINDERED AMINE STABILIZERS, Journal of polymer science. Part A, Polymer chemistry, 35(13), 1997, pp. 2599-2605
Polyoctenamer reacts with singlet oxygen to produce polymeric pendant
hydroperoxide groups. Anthracene was used as a sensitizer for producti
on of singlet oxygen under 365 nm irradiation. Remarkable differences
were observed when the reaction was performed in the solid state or in
the solution. Hydroperoxidation in the solution was much slower than
in the film, and only pendant hydroperoxides were produced. Conversely
, two processes take place in the film. One is the ''ene'' reaction of
singlet oxygen with double bonds producing hydroperoxides as in the s
olution; the second one is a radical process producing both carbonyl p
roducts and additional hydroperoxides. This process went on after anth
racene was completly consumed. Irradiation (lambda > 300 nm) of hydrop
eroxidized polyoctenamer solution in the presence of monomers ( 2,2,6,
6-tetramethyl or 1,2,2,6,6-pentamethyl-4-piperidyl acrylate) or stable
nitroxyl radicals ( earoyloxy-2,2,6,6-tetramethyl-4-piperidyl-4-N-oxy
l or TEMPO) grafted these monomers or stable radicals onto the polyoct
enamer. Light stabilizing efficiency of grafted and low molecular addi
tives was tested in polyoctenamer. (C) 1977 John Wiley & Sons, Inc.