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Darstellung neuartiger monomerer, oligomerer und polymerer Silyltriflate
Author(s) -
Uhlig Wolfram
Publication year - 1992
Publication title -
chemische berichte
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 0009-2940
DOI - 10.1002/cber.19921250109
Subject(s) - organosilicon , chemistry , trifluoromethanesulfonate , silylation , silanes , silicon , polymer chemistry , monomer , medicinal chemistry , reagent , organic chemistry , catalysis , polymer , silane
Preparation of New Monomeric, Oligomeric, and Polymeric Silyl Triflates The highly reactive silyl triflates R 3 SiOSO 2 CF 3 are valuable reagents in organosilicon chemistry. New triflate derivatives of mono‐ and oligosilanes have been prepared by substitution of phenyl groups or hydrogen atoms for the trifluoromethanesulfonyl group. The presence of the electron‐withdrawing triflate group leads to a strong deactivation of the other substituents at the silicon atom, and the displacement of a second phenyl group at the same silicon atom is much slower than the first step. For this reason in the case of phenylated oligosilanes stepwise monosubstitution of the silicon atoms has been found. Other new oligomeric silyl triflates are obtained by reaction of silanediyl(triyl) bis(tris)(trifluoromethanesulfonates) with lithium derivatives of organosilicon compounds. Finally, the cleavage of silicon–phenyl bonds of poly[methyl(phenyl)silanes] by CF 3 SO 3 H leads to triflate derivatives of polysilanes.

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