K. Matsukawa et al., FREE-RADICAL COPOLYMERIZATION OF ALLYLOXYPHENYLSILOXANES WITH SOME VINYL MONOMERS, Die Angewandte makromolekulare Chemie, 215, 1994, pp. 147-160
Two p-allyloxyphenyldisiloxane compounds, (p-allyloxyphenyl)-1,1,3,3,3
-pentamethyldisiloxane (mono-APDS) and is(p-allyloxyphenyl)-1,1,3,3-te
tramethyldisiloxane (bis-APDS), were synthesized to study their radica
l copolymerizations with some vinyl monomers (styrene, methyl methacry
late, N-phenylmaleimide and maleic anhydride). The reactivities of all
yl groups in mono-APDS and bis-APDS were found to be almost the same i
n styrene and methyl methacrylate copolymerization, as evidenced by th
eir composition curves, and increase with the electron-accepting abili
ty of comonomers. In the case of electron-poor monomers, such as N-phe
nylmaleimide and maleic anhydride, the second allyl group of bis-APDS
readily took part in the crosslinking. Differential scanning calorimet
ry and thermogravimetry revealed that the increase of APDS contents in
those copolymers led to lower glass transition temperature (T(g)) and
higher thermal degradation temperature.