Ns. Allen et al., PHOTOPOLYMERIZATION AND PHOTOCHEMISTRY OF NOVEL PHOTOINITIATORS BASEDON P-BENZOYLBENZOPHENONE, European Polymer Journal, 29(11), 1993, pp. 1473-1475
Six novel derivatives based on the p-benzoylbenzophenone chromophore h
ave been examined in terms of their photochemical and photoinitiator p
roperties, All the molecules exhibit high extinction coefficients in t
he u.v. region together with high photoinitiator activity for the poly
merization of methyl methacrylate. The 2-substituted methyl and isopro
pyl derivatives exhibited the lowest activity, consistent with lower p
hosphorescence quantum yields and ketyl radical formation on microseco
nd flash photolysis compared with the corresponding 4-substituted deri
vatives. In the case of 2-substitution with an isopropyl group, ketyl
radical formation was not quenched by oxygen indicating that a process
of intra-molecular hydrogen atom abstraction predominates. This deriv
ative was also less effective than benzophenone as a photoinitiator. A
nalysis of the photoproducts in 2-propanol confirmed the involvement o
f a single step reaction to give a corresponding pinnacol type compoun
d.