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  2. Dimethyldichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Dimethyldichlorosilane

    The main purpose of dimethyldichlorosilane is for use in the synthesis of silicones, an industry that was valued at more than $10 billion per year in 2005. It is also employed in the production of polysilanes, which in turn are precursors to silicon carbide . [ 3 ]

  3. Silanes - Wikipedia

    en.wikipedia.org/wiki/Silanes

    The dominant examples come from the Direct process, i.e., (CH 3) 4-x SiCl x. Another important member is trichlorosilane (SiHCl 3). Organosilanes are a class of charge-neutral organosilicon compounds. Example: tetramethylsilane (Si(CH 3) 4) By tradition, compounds with Si-O-Si bonds are usually not referred to as silanes. Instead, they are ...

  4. Direct process - Wikipedia

    en.wikipedia.org/wiki/Direct_process

    The major product for the direct process should be dichlorodimethylsilane, Me 2 SiCl 2. However, many other products are formed. Unlike most reactions, this distribution is actually desirable because the product isolation is very efficient. [1] Each methylchlorosilane has specific and often substantial applications. Me 2 SiCl 2 is the most ...

  5. List of metal-organic chemical vapour deposition precursors

    en.wikipedia.org/wiki/List_of_metal-organic...

    Thus, much effort has been aimed at the synthesis of new molecular precursors. A productive overview is provided by several exceptional reviews covering fields of MOCVD such as, for instance, epitaxial growth of semiconductor compounds, [2] [3] [4] and low temperature deposition of metals.

  6. Chlorosilane - Wikipedia

    en.wikipedia.org/wiki/Chlorosilane

    Other acid-forming species, especially acetate, can replace chlorine in silicone synthesis with little difference in the chemistry of the finished polymer. These analogues of chlorosilanes are quite common in the sealants and adhesives marketed to consumers, and as precursors for medical-grade silicone, because of reduced toxicity.

  7. Hydrosilanes - Wikipedia

    en.wikipedia.org/wiki/Hydrosilanes

    One example is triethoxysilane: HSiCl 3 + 3 EtOH → HSi(OEt) 3 + 3 HCl. Organohydrosilanes can be prepared by partial hydrosilation of silane itself: SiH 4 + 3 C 2 H 4 → HSi(C 2 H 5) 3. In the laboratory, hydrosilanes classically are prepared by treating chlorosilanes with hydride reagents, such as lithium aluminium hydride:

  8. Organosilicon chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosilicon_chemistry

    Although proportionately a minor outlet, organosilicon compounds are widely used in organic synthesis. Notably trimethylsilyl chloride Me 3 SiCl is the main silylating agent. One classic method called the Flood reaction for the synthesis of this compound class is by heating hexaalkyldisiloxanes R 3 SiOSiR 3 with concentrated sulfuric acid and a ...

  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.