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Disilane, hexachloro

Inverted names are used only for derivatives of silanes (as Silane, dibromo- and Disilane, hexachloro-), germanes, phosphine, and the like, but not for the few organic compounds. For the nomenclature of some of these and other classes of compounds, see the heading Nomenclature. [Pg.223]

Bis(trichlorosilyl)nickel(II) complex 4, having an r/ -arene hgand,is prepared by reaction of hexachloro disilane with highly reactive, vaporized nickel in the presence of toluene (Eq. 2) [12]. Worthy of note is that the arene ligand is displaced by three molecules of carbon monoxide to give 5 [13]. [Pg.133]

Preparation.1 The reagent (1) is prepared by the reaction of hexachloro-disilane and a mixture of trimethyl orthoformate and methanol ... [Pg.257]

Sulfur Diimide Reduction. iV-Trichlorosilyldiaininosulfanes were prepared upon treatment of sulfur diimides with hexachloro-disilane (eq 9). Likewise, the corresponding IV-dichloromethyl-silyldiaminosulfanes resulted by substituting 1,2-dimethyl-1,1,2,2-tetrachlorodisilane for hexachlorodisilane. [Pg.310]


See other pages where Disilane, hexachloro is mentioned: [Pg.205]    [Pg.408]    [Pg.551]    [Pg.647]    [Pg.788]    [Pg.205]    [Pg.408]    [Pg.551]    [Pg.647]    [Pg.788]    [Pg.23]   
See also in sourсe #XX -- [ Pg.42 ]

See also in sourсe #XX -- [ Pg.42 ]




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Disilane

Disilanes

Hexachloro

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