The copolymerization behaviour of 1,3-divinyl-1,1,3,3-tetramethyldisil
oxane (DVDS) with styrene in solution, using a free radical initiator,
was investigated. Styrene was found to be the more reactive monomer.
The FTi.r. and Si-29 n.m.r. spectra indicated that cyclic units were f
ormed from DVDS in the copolymer, with five-and six-membered ring stru
ctures being common. The cyclocopolymerization mechanisms and the ther
mal properties of the cyclocopolymer are reported. (C) 1997 Elsevier S
cience Ltd. All rights reserved.