Organopolysiloxan-,Polykarbonat-Copolymere sowie Verfahren zu ihrer Herstellung

1,175,264. Organopolysiloxane - polycarbonate block copolymers. GENERAL ELECTRIC CO. 22 Dec., 1966 [3 Jan., 1966], No. 57587/66. Heading C3T. Organopolysiloxane - polycarbonate block copolymers have unsaturated terminal groups V1-OCOO- or V1-NHCOO- and comprise 1-95 wt. per cent of (A) polysiloxane blocks of units R1 2 SiO and correspondingly 5-99 wt. per cent of (B) blocks of the reaction product of a compound HO-Z-OH with a carbonyl halide or diaryl carbonate, the blocks (A) and (B) being linked by groups -R11-COO-, -R11-NHCOO-, -R11-OCONH-R11- NHCOO- or -COO-, in which R11 or the C atom is linked to Si, or by -O- or -OCOO- joining a silicon atom to a group Z; wherein V1 is an olefinic or acetylenic optionally halogenated aliphatic or cycloaliphatic monovalent hydrocarbon radical. In examples, a chlorine-terminated polydimethylsiloxane is reacted with an excess of bisphenol A, in Example 6 after an initial reaction with diphenylol sulphone, then with phosgene; the end groups derive from allyl alcohol (allyl phenol in Example 3) added partly before, partly after the phosgenation, or allyl isocyanate (Example 1) added after; the products contain 61-64% polysiloxane, curing to elastomers, or 15% polysiloxane (Example 5) curing rigid. The products of Examples 2 and 3 are reacted with methyldiacetoxysilane in toluene i.p.o. a Pt catalyst to give a solution which cures in moist air, after addition of stannous octoate or dibutyltin dilaurate catalyst; the product of Example 4 is milled with fume silica and dicumyl peroxide and cured to a rubber.