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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. 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.

  4. Silanes - Wikipedia

    en.wikipedia.org/wiki/Silanes

    Silanes with one, two, three, or four Si-H bonds are called hydrosilanes. Silane is again the parent member. Examples: triethylsilane (HSi(C 2 H 5) 3) and triethoxysilane (HSi(OC 2 H 5) 3). Polysilanes are organosilicon compounds with the formula (R 2 Si) n. They feature Si-Si bonds. Attracting more interest are the organic derivatives such as ...

  5. Silanol - Wikipedia

    en.wikipedia.org/wiki/Silanol

    Silanols are more acidic than the corresponding alcohols. This trend contrasts with the fact that Si is far less electronegative than carbon (1.90 vs 2.55, respectively). For Et 3 SiOH, the pK a is estimated at 13.6 vs. 19 for tert-butyl alcohol. The pK a of 3−ClC 6 H 4)Si(CH 3) 2 OH is 11. [3]

  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. Methyltrichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Methyltrichlorosilane

    MeSiCl 3 + 3 H 2 O → MeSi(OH) 3 + 3 HCl. The silanol is unstable and will eventually condense to give a polymer network: MeSi(OH) 3 → MeSiO 1.5 + 1.5 H 2 O. Methyltrichlorosilane undergoes alcoholysis (reaction with alcohol) to give alkoxysilanes. Methanol converts it to trimethoxymethylsilane: MeSiCl 3 + 3 CH 3 OH → MeSi(OCH 3) 3 + 3 HCl

  8. Methyltrimethoxysilane - Wikipedia

    en.wikipedia.org/wiki/Methyltrimethoxysilane

    Density: 0.955 g/cm 3: Boiling point: 102–104 °C (216–219 °F; 375–377 K) ... Methyltrimethoxysilane is an organosilicon compound with the formula CH 3 Si(OCH ...

  9. Trimethylsilanol - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilanol

    TMS is a contaminant in the atmospheres of spacecraft, where it arises from the degradation of silicone-based materials. [5] Specifically, it is the volatile product from the hydrolysis of polydimethylsiloxane, which are generally terminated with trimethylsilyl groups: (CH 3) 3 SiO[Si(CH 3) 2 O] n R + H 2 O → (CH 3) 3 SiOH + HO[Si(CH 3) 2 O] n R