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  2. Dichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Dichlorosilane

    Dichlorosilane, or DCS as it is commonly known, is a chemical compound with the formula H 2 SiCl 2. In its major use, it is mixed with ammonia (NH 3 ) in LPCVD chambers to grow silicon nitride in semiconductor processing.

  3. Chlorosilane - Wikipedia

    en.wikipedia.org/wiki/Chlorosilane

    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 preparation of silane: SiCl 4 + LiAlH 4 → SiH 4 ...

  4. Dimethyldichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Dimethyldichlorosilane

    The mechanism of the direct synthesis is not known. However, the copper catalyst is essential for the reaction to proceed. In addition to dimethyldichlorosilane, products of this reaction include CH 3 SiCl 3, CH 3 SiHCl 2, and (CH 3) 3 SiCl, which are separated from each other by fractional distillation. The yields and boiling points of these ...

  5. Difluorosilane - Wikipedia

    en.wikipedia.org/wiki/Difluorosilane

    Difluorosilane can be made by fluorinating dichlorosilane with antimony trifluoride. [2] [3] 3 SiH 2 Cl 2 + 2 SbF 3 → 3 SiH 2 F 2 + 2 SbCl 3. Some is also made in a reaction of silicon tetrafluoride with hydrogen. SiF 4 + 2 H 2 → SiH 2 F 2 + 2 HF. Traces of difluorosilane are made when coal is burnt. [4]

  6. RTV silicone - Wikipedia

    en.wikipedia.org/wiki/RTV_silicone

    The silicone polymers are often made by reacting dimethyl dichlorosilane with water. [4] Linear dimethylpolysiloxane polymer reaction. Fillers such as acetic acid can provide a fast cure time, while oxides and nitrides can provide better thermal conductivity. Tack-free times are typically on the order of minutes, with cure times on the order of ...

  7. Trichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Trichlorosilane

    Trichlorosilane is a reagent in the conversion of benzoic acids to toluene derivatives. In the first step of a two-pot reaction, the carboxylic acid is first converted to the trichlosilylbenzyl compound. In the second step, the benzylic silyl derivative is converted to the toluene derivative with base. [7]

  8. Trimethylsilyl group - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_group

    When attached to certain functional groups in a reactant molecule, trimethylsilyl groups may also be used as temporary protecting groups during chemical synthesis or some other chemical reactions. In chromatography, derivitization of accessible silanol groups in a bonded stationary phase with trimethylsilyl groups is referred to as endcapping.

  9. Chlorodimethylsilane - Wikipedia

    en.wikipedia.org/wiki/Chlorodimethylsilane

    Chlorodimethylsilane, also called dimethylchlorosilane and abbreviated DMCS, is a chemical compound with the formula (CH 3) 2 SiHCl. It is a silane, with a silicon atom bonded to two methyl groups, a chlorine atom, and a hydrogen atom.