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  2. Dimethyldichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Dimethyldichlorosilane

    Dimethyldichlorosilane is a tetrahedral organosilicon compound with the formula Si(CH 3) 2 Cl 2. At room temperature it is a colorless liquid that readily reacts with water to form both linear and cyclic Si-O chains. Dimethyldichlorosilane is made on an industrial scale as the principal precursor to dimethylsilicone and polysilane compounds.

  3. Dichlorobis(triphenylphosphine)nickel(II) - Wikipedia

    en.wikipedia.org/wiki/Dichlorobis(triphenylphosp...

    Dichlorobis(triphenylphosphine)nickel(II) refers to a pair of metal phosphine complexes with the formula NiCl 2 [P(C 6 H 5) 3] 2. The compound exists as two isomers, a paramagnetic dark blue solid and a diamagnetic red solid. These complexes function as catalysts for organic synthesis. [1]

  4. Bis(triphenylphosphine)palladium chloride - Wikipedia

    en.wikipedia.org/wiki/Bis(triphenylphosphine...

    Several crystal structures containing PdCl 2 (PPh 3) 2 have been reported. In all of the structures, PdCl 2 (PPh 3) 2 adopts a square planar coordination geometry and the trans isomeric form. [5] [6] [7] [8]

  5. Chlorosilane - Wikipedia

    en.wikipedia.org/wiki/Chlorosilane

    2 ((CH 3) 3 SiCl + H 2 O → [(CH 3) 3 Si] 2 O + 2 HCl. The analogous reaction of dimethyldichlorosilane gives siloxane polymers or rings: n (CH 3) 2 SiCl 2 + n H 2 O → [(CH 3) 2 SiO] n + 2n HCl. Many compounds containing Si-Cl bonds can be converted to hydrides using lithium aluminium hydride, This kind of conversion was demonstrated for the ...

  6. Methyltrichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Methyltrichlorosilane

    [1] 2 CH 3 Cl + Si → (CH 3) 4−n SiCl n + other products. While this reaction is the standard in industrial silicone production and is nearly identical to the first direct synthesis of methyltrichlorosilane, the overall process is inefficient with respect to methyltrichlorosilane. [2]

  7. Dichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Dichlorosilane

    Stock and Somieski completed the hydrolysis of dichlorosilane by putting the solution of H 2 SiCl 2 in benzene in brief contact with a large excess of water. [3] [5] A large-scale hydrolysis was done in a mixed ether/alkane solvent system at 0 °C, which gave a mixture of volatile and nonvolatile [H 2 SiO] n.

  8. Trimethylsilyl group - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_group

    This group consists of three methyl groups bonded to a silicon atom [−Si(CH 3) 3], which is in turn bonded to the rest of a molecule. This structural group is characterized by chemical inertness and a large molecular volume , which makes it useful in a number of applications.

  9. Sodium bis(trimethylsilyl)amide - Wikipedia

    en.wikipedia.org/wiki/Sodium_bis(trimethylsilyl...

    NaN(Si(CH 3) 3) 2 Molar mass: 183.377 g·mol −1 Appearance off-white solid Density: 0.9 g/cm 3, solid Melting point: 171 to 175 °C (340 to 347 °F; 444 to 448 K) Boiling point: 202 °C (396 °F; 475 K) 2 mmHg