F. Koopmann et al., POLY(METHYLPHENYLSILYLENEMETHYLENE) - THE CARBOSILANE ANALOG OF POLY(ALPHA-METHYLSTYRENE), Acta polymerica, 47(9), 1996, pp. 377-385
The carbosilane analog of poly(alpha-methylstyrene), poly(methylphenyl
silylenemethylene) (PMPSM) has been prepared by ring-opening polymeriz
ation of 1,3-dimethyl-1,3-diphenyl-1,3-disilacyclobutane (1), using va
rious transition-metal-based catalysts in bulk and in solution. PMPSM
samples from polymerization in bulk and in solution, respectively, wer
e characterized by GPC coupled with on-line low-angle laser light scat
tering (LALLS) and viscometry. Absolute molecular weights were in the
range of 200 000; however, polymerization in solution afforded higher
yields of PMPSM. Polymerizations generally yielded atactic PMPSM with
strictly alternating SiR(1)R(2)/CH2 backbone structure and monomodal m
olecular weight distribution. Radical and cationic initiators proved t
o be unable to effect polymerization. Polymerization of pure trans-1 a
fforded PMPSM without isotactic triads. Stereoregularity as well as po
lymer yields increased when polymerization was performed at low temper
atures (-32 degrees C). Thermal properties of PMPSM were investigated.
TGA analysis evidenced better thermal stability of PMPSM than poly(al
pha-methylstyrene). PMPSM shows a T-g at 28 degrees C, which lies betw
een the glass transition of poly(alpha-methylstyrene) and that of poly
(methylphenylsiloxane), suggesting that poly(silylenemethylenes) may s
tructurally be ranged between the analogous carbon-based polymers and
the highly flexible poly(siloxanes).