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Silenes and Silenoids in the Chemistry of Cyclopentadienylsilanes

Evidence is presented that apparent silene products obtained from the metalation of cyclopentadienyldimethyl - chlorosilane either with tert-butyl1ithium or with methylenetriphenylphosphorane actually arise from the metalated starting material, a silenoid, rather than from a silafulvene intermediate. Trimethylmethoxysi1ane is shown to be an effective trap for dimethylsilafulvene. A new dimethylsilafulvene precursor, bis(dimethylmethoxysi1yl) cyclopentadiene, which gives high yields of dimethyldimethoxysi1ane and the silafulvene at temperatures as low as 240°C is reported.

Identiferoai:union.ndltd.org:unt.edu/info:ark/67531/metadc331302
Date08 1900
CreatorsRozell, James M. (James Morris)
ContributorsJones, Paul R., Conlin, Robert T., Thomas, Ruthanne D., Tarter, James G.
PublisherNorth Texas State University
Source SetsUniversity of North Texas
LanguageEnglish
Detected LanguageEnglish
TypeThesis or Dissertation
Formatvi, 109 leaves: ill., Text
RightsPublic, Rozell, James M. (James Morris), Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved.

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