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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. Trimethylsilanol - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilanol

    The heat of evaporation is 45.64 kJ·mol −1, the evaporation entropy 123 J·K1 ·mol −1. [2] The vapor pressure function according to Antoine is obtained as log 10 (P/1 bar) = A − B/(T + C) (P in bar, T in K) with A = 5.44591, B = 1767.766 K and C = −44.888 K in a temperature range from 291 K to 358 K. [ 2 ] Below the melting point ...

  4. 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.

  5. 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]

  6. 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 ...

  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. m-Xylene - Wikipedia

    en.wikipedia.org/wiki/M-Xylene

    The m-stands for meta-, indicating that the two methyl groups in m-xylene occupy positions 1 and 3 on a benzene ring. It is in the positions of the two methyl groups, their arene substitution pattern, that it differs from the other isomers, o-xylene and p-xylene. All have the same chemical formula C 6 H 4 (CH 3) 2. All xylene isomers are ...

  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