FORMATION OF ORGANOSILICON COMPOUNDS 115 - THE APPLICABILITY AS PRECURSORS FOR BETA-SIC OF CARBOSILANES RESULTING FROM THE GAS-PHASE PYROLYSIS OF METHYLSILANES
D. Togel et al., FORMATION OF ORGANOSILICON COMPOUNDS 115 - THE APPLICABILITY AS PRECURSORS FOR BETA-SIC OF CARBOSILANES RESULTING FROM THE GAS-PHASE PYROLYSIS OF METHYLSILANES, Journal of organometallic chemistry, 521(1-2), 1996, pp. 125-131
The thermal properties of polycarbosilanes from the gas phase pyrolysi
s of SiMe(4), Me(3)SiCl, Me(2)SiCl(2) and the polymeric (Me(2)Si-CH2)(
n) has been investigated. They decompose above 400 degrees C to form v
olatile methylsilanes, H-2, CH4, viscous carbosilanes and insoluble gl
assy products via condensation reactions, The ceramic yield is between
10 and 20 wt.% at about 900 degrees C and falls to only a few weight
per cent when heating is continued to 1000 degrees C. The gas phase py
rolysis of Me(2)SiH(2) at 650 degrees C produces plastic, meltable pol
ycarbosilanes (PCS). Tempering the compounds to 900 degrees C gives a
ceramic residue in 85% yield with Si:C:H 1:1.2:0.4, Heating this resid
ue under thermal gravimetry (TG) conditions to 1500 degrees C (argon a
tmosphere) results in a further weight loss of 0.7% and formation of b
eta-SiC. Silicon carbide is also formed when the PCS from Me(2)SiH(2)
(Si:C:H 1:1.5:2.5) are heated to 1400 degrees C, with a weight loss of
16.3% under nitrogen and one of 42% in vacuum.