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Cyclic oligosilanes, synthesis

A second useful precursor for the synthesis of sterically overcrowded oligosilyl anions is octakis(trimethylsilyl)tetrasilacyclobutane (8) [3], a cyclic oligosilane which can easily be converted into HTSB-K (9) by selective cleavage of the Si-SiMes bond with rBuOK in THF [4], After removal of the solvent, a highly moisture- and air-sensitive yellow-orange powder was obtained, which could be identified by NMR spectroscopy as the THF adduct of 9 (Scheme 2). [Pg.219]

Many cyclic and linear transition metal-silicon compounds have been obtained by the elimination of alkali halides with the corresponding transition metal salts145,146. The synthesis and reactivity of the Fe-oligosilane systems have been studied in detail by Pannell147-154 and this area has been recently reviewed155. [Pg.2083]


See other pages where Cyclic oligosilanes, synthesis is mentioned: [Pg.410]    [Pg.144]    [Pg.374]    [Pg.374]    [Pg.217]    [Pg.300]    [Pg.200]    [Pg.201]   
See also in sourсe #XX -- [ Pg.1211 , Pg.1212 , Pg.1213 , Pg.1214 , Pg.1215 , Pg.1216 , Pg.1217 , Pg.1218 , Pg.1219 ]




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