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  2. Poly(4-vinylphenol) - Wikipedia

    en.wikipedia.org/wiki/Poly(4-vinylphenol)

    Poly(4-vinylphenol), also called polyvinylphenol or PVP, is a plastic structurally similar to polystyrene. It is produced from the monomer 4-vinylphenol, which is also referred to as 4-hydroxystyrene. PVP is used in electronics as a dielectric layer in organic transistors in organic TFT LCD displays.

  3. Poly(p-phenylene vinylene) - Wikipedia

    en.wikipedia.org/wiki/Poly(p-phenylene_vinylene)

    Poly(p-phenylene vinylene) (PPV, or polyphenylene vinylene) is a conducting polymer of the rigid-rod polymer family. PPV is the only polymer of this type that can be processed into a highly ordered crystalline thin film. PPV and its derivatives are electrically conducting upon doping.

  4. Dendrimer - Wikipedia

    en.wikipedia.org/wiki/Dendrimer

    Crystal structure of a first-generation polyphenylene dendrimer reported by Müllen et al [5] A first-generation "cyanostar" dendrimer and its STM image [6]. The first dendrimers were made by divergent synthesis approaches by Fritz Vögtle in 1978, [7] R.G. Denkewalter at Allied Corporation in 1981, [8] [9] Donald Tomalia at Dow Chemical in 1983 [10] and in 1985, [11] [12] and by George R ...

  5. Polyphenol - Wikipedia

    en.wikipedia.org/wiki/Polyphenol

    The name derives from the Ancient Greek word πολύς (polus, meaning "many, much") and the word ‘phenol’ which refers to a chemical structure formed by attachment of an aromatic benzenoid ring to a hydroxyl (-OH) group (hence the -ol suffix). The term "polyphenol" has been in use at least since 1894.

  6. Anionic addition polymerization - Wikipedia

    en.wikipedia.org/.../Anionic_addition_polymerization

    In polymer chemistry, anionic addition polymerization is a form of chain-growth polymerization or addition polymerization that involves the polymerization of monomers initiated with anions. The type of reaction has many manifestations, but traditionally vinyl monomers are used.

  7. 4-Vinylphenol - Wikipedia

    en.wikipedia.org/wiki/4-vinylphenol

    In wine, 4-vinylphenol can react with other molecules, such as anthocyanidins, to produce new chemical compounds. [2] In white wines vinylphenols are dominant (4-vinylphenol 70-1 150 μg/L, 4-vinylguaiacol 10-490 μg/L) whereas, in red wines, it is the corresponding ethyl phenols .

  8. Reversible-deactivation radical polymerization - Wikipedia

    en.wikipedia.org/wiki/Reversible-deactivation...

    There is a mode of polymerization referred to as reversible-deactivation polymerization which is distinct from living polymerization, despite some common features. Living polymerization requires a complete absence of termination reactions, whereas reversible-deactivation polymerization may contain a similar fraction of termination as conventional polymerization with the same concentration of ...

  9. Vinylene group - Wikipedia

    en.wikipedia.org/wiki/Vinylene_group

    In chemistry, vinylene (also ethenylene or 1,2-ethenediyl) [1] is a divalent functional group (a part of a molecule) [2] with formula −CH=CH−; [3] namely, two carbons, each connected to the other by a double bond, to an hydrogen atom by a single bond, and to the rest of the molecule by another single bond.