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Silicon-transition-metal complexes halogen compounds

Whereas most of the known silylamines containing both a silicon halogen and nitrogen hydrogen unit undergo rapid condensation with HC1 elimination [11], transition metal substitution of the silicon provides unexpected high thermal stability. Compounds of this type are available via reaction of the dichlorosilyl complexes 18a-c with bulky primary amines to generate 19a-c (Eq. (4)). [Pg.189]

Transition-metal catalyzed metathesis of carbon-halogen bonds with Si-Si bonds provides useful access to organosilicon compounds. Most of the reaction may involve initial oxidative addition of the carbon-halogen bond onto the transition-metal followed by activation of the Si-Si bond to give (organosilyl)(orga-no)palladium(II) complex, which undergoes reductive elimination of the carbon-silicon bond. [Pg.153]


See other pages where Silicon-transition-metal complexes halogen compounds is mentioned: [Pg.308]    [Pg.26]    [Pg.281]    [Pg.239]    [Pg.103]    [Pg.150]    [Pg.583]    [Pg.351]    [Pg.231]   
See also in sourсe #XX -- [ Pg.40 , Pg.48 ]

See also in sourсe #XX -- [ Pg.40 , Pg.48 ]




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Halogen complexes Halogens

Halogen compounds

Halogenation compounds

Halogens, complex compounds

Metal-halogen

Metallic silicon

Silicon complexes

Silicon transition metals

Silicon-metal complexes

Silicon-transition-metal complexes

Siliconates complex

Silicone compounds

Transition compounds

Transition-metal compounds

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