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Hypersilyl group

The hypersilyl group allows isolation of stable gallium silyl compounds with tri- and tetracoordinated gallium centres. The GaSi bond seems to be inert to protic reagents. [Pg.529]

Methoxy-bis[tris(trimethylsilyl)silyl]methane (4) - the first compound bearing two hypersilyl groups at a carbon atom - was synthesized by the reaction of tris(trimethylsilyl)silyllithium (1) with dichloromethyl methyl ether in a yield of 35 % In view of the extreme bulkiness of the two hypersilyl substituents, the ease of the formation of 4 is really surprising. But the reaction pathway is easily understood as a consecutive replacement of the two chlorine atoms of the dichloromethyl methyl ether by the silanide 1 (Eq. 1). [Pg.178]

Keywords Hypersilyl / Group 15 Cages / Cyclotrisilane / Crystal Structure... [Pg.367]

The synthesis of tris(trimethylsilyl)silylphosphine (Scheme 2) yielded colorless crystals that could easily be purified by vacuum sublimation. Contrary to the observations made by Uhlig [3] with the Si(CH3)3 substituent, we were not able to introduce more than one bulky hypersilyl group to PHj. [Pg.371]


See other pages where Hypersilyl group is mentioned: [Pg.159]    [Pg.115]    [Pg.290]    [Pg.298]    [Pg.303]    [Pg.326]    [Pg.328]    [Pg.247]    [Pg.283]    [Pg.143]    [Pg.151]    [Pg.156]    [Pg.179]    [Pg.181]    [Pg.178]    [Pg.179]    [Pg.185]    [Pg.185]    [Pg.133]    [Pg.137]    [Pg.207]    [Pg.208]    [Pg.356]   
See also in sourсe #XX -- [ Pg.3 , Pg.493 , Pg.525 ]




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Hypersilyl

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