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  2. Negative hyperconjugation in silicon - Wikipedia

    en.wikipedia.org/wiki/Negative_hyperconjugation...

    The silicon effect also manifests in certain compound properties. Trimethylsilylmethylamine (Me 3 SiCH 2 NH 2) is a stronger base (conjugate pK a 10.96) than neopentylamine (conjugate pK a 10.21); trimethylsilylacetic acid (pKa 5.22) is a poorer acid than trimethylacetic acid (pKa 5.00). [1]

  3. Negative hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Negative_hyperconjugation

    Negative hyperconjugation is seldom observed, though it can be most commonly observed when the σ *-orbital is located on certain C–F or C–O bonds. [ 3 ] [ 4 ] In negative hyperconjugation, the electron density flows in the opposite direction (from a π- or p-orbital to an empty σ * -orbital) than it does in the more common ...

  4. Does Oil Pulling for Teeth Actually Work? Dentists Explain ...

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    Oil-pulling side effects. The risks of oil pulling are generally minimal, says Jossen Gastelum, D.M.D., general and cosmetic dentist based in Scottsdale, AZ, who notes that the side effects mostly ...

  5. Polydimethylsiloxane - Wikipedia

    en.wikipedia.org/wiki/Polydimethylsiloxane

    It is one of several types of silicone oil (polymerized siloxane). The applications of PDMS range from contact lenses and medical devices to elastomers ; it is also present in shampoos (as it makes hair shiny and slippery ), food ( antifoaming agent ), caulk , lubricants and heat-resistant tiles .

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  7. Hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Hyperconjugation

    Hyperconjugation can be used to rationalize a variety of chemical phenomena, including the anomeric effect, the gauche effect, the rotational barrier of ethane, the beta-silicon effect, the vibrational frequency of exocyclic carbonyl groups, and the relative stability of substituted carbocations and substituted carbon centred radicals, and the thermodynamic Zaitsev's rule for alkene stability.

  8. Silanization - Wikipedia

    en.wikipedia.org/wiki/Silanization

    [1] [2] This process is often used to modify the surface properties of glass, silicon, alumina, quartz, and metal oxide substrates, which all have an abundance of hydroxyl groups. Silanization differs from silylation , which usually refers to attachment of organosilicon groups to molecular substrates.

  9. 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 ]