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1,3-Bis(trichlorosilyl) cyclohexane was obtained by addition of HSiCl_3, to cyclohexadiene-1,3in the presence of H_2PtCl_6.6H_2O in isopropyl alcohol. The new compound was ethanolysed andmethylated to form di-methyl tetra-ethoxy disilyl, tri-methyl tri-ethoxy disilyl and terta-methyldi-ethoxy disilyl cyclohexanes. These di-to tetra-functional monomers were hydrolyzed by hydrochloric acid in ether. The di-functional monomer yielded cyclic dimer similar to octamethylcyclotetrasiloxane and the tri-functionalmonomer, a cyclic tetramer, while in the case of tetra-functional monomer a cyclic octamer wasobtained. These compounds have not been reported in literature.
1,3-Bis (trichlorosilyl) cyclohexane was obtained by addition of HSiCl_3, to cyclohexadiene-1,3 in the presence of H_2PtCl_6.6H_2O in isopropyl alcohol. The new compound was ethanolysed and methylated to form di-methyl tetra-ethoxy disilyl, tri- methyl di-functional monomers were hydrolyzed by hydrochloric acid in ether. The di-functional monomer yielded cyclic dimer similar to octamethylcyclotetrasiloxane and the tri-functionalmonomer, a cyclic tetramer , while in the case of tetra-functional monomer a cyclic octamer wasobtained. These compounds have not been reported in literature.