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Aluminum pentavalent

A mechanism for the GTPase activity has been proposed from the crystal structure of aluminum fluoride (A1F4 ) complex with transducin-a.69 Aluminum fluoride activates transducin-a- GDP by binding with a geometry resembling a pentavalent intermediate for GTP hydrolysis. [Pg.496]

In many ways the phosphates provide the richest field for CBC s (chemically bonded ceramics) because of the P—O bond strengths and the coordination demands of pentavalent phosphorus. Among silicates, room temperature hydration reactions seem to be possible only with Ca-compounds the magnesium and aluminum anhydrous silicates phases simply do not react. This book documents for the reader the wide application of these separate chemistries as true chemically bonded ceramics. [Pg.291]

Recently, hydrocyanation and cyanosilylation reactions with other type of chiral aluminum complexes were reported. In 1999, Shibasaki and Kanai reported enantioselective cyanosilylation of aldehydes catalyzed by Lewis acid-Lewis base bifunctional catalyst (64a) [56, 57]. In this catalyst, aluminum center works as a Lewis acid to activate the carbonyl group, and the oxygen atom of the phosphine oxide works as a Lewis base to activate TMSCN. Asymmetric induction was explained by the proposed transition state model having the external phosphine oxide coordination to aluminum center, thus giving rise to pentavalent aluminum... [Pg.266]


See other pages where Aluminum pentavalent is mentioned: [Pg.118]    [Pg.335]    [Pg.221]    [Pg.162]    [Pg.3756]    [Pg.399]    [Pg.294]    [Pg.285]    [Pg.275]    [Pg.3755]    [Pg.719]    [Pg.184]    [Pg.1338]    [Pg.594]    [Pg.154]    [Pg.118]    [Pg.280]   
See also in sourсe #XX -- [ Pg.266 ]




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Pentavalent

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