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  2. Silicone - Wikipedia

    en.wikipedia.org/wiki/Silicone

    Silicone caulk can be used as a basic sealant against water and air penetration. In organosilicon and polymer chemistry, a silicone or polysiloxane is a polymer composed of repeating units of siloxane (−O−R 2 Si−O−SiR 2 −, where R = organic group). They are typically colorless oils or rubber-like substances. Silicones are used in ...

  3. Siloxane - Wikipedia

    en.wikipedia.org/wiki/Siloxane

    In organosilicon chemistry, a siloxane is an organic compound containing a functional group of two silicon atoms bound to an oxygen atom: Si−O−Si. The parent siloxanes include the oligomeric and polymeric hydrides with the formulae H[OSiH 2 ] n OH and [OSiH 2 ] n . [ 1 ]

  4. Silicone resin - Wikipedia

    en.wikipedia.org/wiki/Silicone_resin

    Silicone resin with R = CH 3, H or OH. Silicone resins are a type of silicone material which is formed by branched, cage-like oligosiloxanes with the general formula of R n SiX m O y, where R is a non-reactive substituent, usually methyl (Me = −CH 3) or phenyl (Ph = −C 6 H 5), and X is a functional group: hydrogen (−H), hydroxyl (−OH), chlorine (−Cl) or alkoxy (−O −).

  5. Polydimethylsiloxane - Wikipedia

    en.wikipedia.org/wiki/Polydimethylsiloxane

    Polydimethylsiloxane (PDMS), also known as dimethylpolysiloxane or dimethicone, is a silicone polymer with a wide variety of uses, from cosmetics to industrial lubrication and passive daytime radiative cooling.

  6. Disiloxane - Wikipedia

    en.wikipedia.org/wiki/Disiloxane

    Disiloxanes can be used as sealants for construction, paints, inks, and coatings, cosmetics, mechanical fluids, textile applications, and paper coatings. Commercial use of disiloxane is common in cosmetics. It is commonly found in products such as sunscreen, moisturizer, hair spray, eye liner, body spray, nail polish, makeup remover, and ...

  7. Organosilicon chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosilicon_chemistry

    The C–Si bond is somewhat polarised towards carbon due to carbon's greater electronegativity (C 2.55 vs Si 1.90), and single bonds from Si to electronegative elements are very strong. [14] Silicon is thus susceptible to nucleophilic attack by O −, Cl −, or F −; the energy of an Si–O bond in particular is strikingly high.