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  2. Sodium naphthalene - Wikipedia

    en.wikipedia.org/wiki/Sodium_naphthalene

    Sodium naphthalene is an organic salt with the chemical formula Na + [C 10 H 8] −. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. When isolated, it invariably crystallizes as a solvate with ligands bound to Na +. [1]

  3. Naphthalene - Wikipedia

    en.wikipedia.org/wiki/Naphthalene

    With alkali metals, naphthalene forms the dark blue-green radical anion salts such as sodium naphthalene, Na + C 10 H − 8. The naphthalene anions are strong reducing agents. Naphthalene can be hydrogenated under high pressure in the presence of metal catalysts to give 1,2,3,4-tetrahydronaphthalene(C 10 H 12), also known as tetralin.

  4. Naphthalenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Naphthalenesulfonate

    Naphthalenesulfonates are derivatives of sulfonic acid which contain a naphthalene functional unit. A related family of compounds are the aminonaphthalenesulfonic acids.Of commercial importance are the alkylnaphthalene sulfonates, which are used as superplasticizers in concrete.

  5. Anionic addition polymerization - Wikipedia

    en.wikipedia.org/wiki/Anionic_addition...

    [5] [6] In one of the breakthrough events in the field of polymer science, Szwarc elucidated that electron transfer occurred from radical anion sodium naphthalene to styrene. The results in the formation of an organosodium species, which rapidly added styrene to form a "two – ended living polymer."

  6. Aminonaphthalenesulfonic acids - Wikipedia

    en.wikipedia.org/wiki/Aminonaphthalenesulfonic_acids

    Aminonaphthalenesulfonic acids are compounds with the composition C 10 H 6 (NH 2)(SO 3 H), being derived from naphthalene (C 10 H 8) substituted by an amino and sulfonic acid groups. These compounds are colorless solids. They are useful precursors to dyes. [1]

  7. Category:Naphthalenes - Wikipedia

    en.wikipedia.org/wiki/Category:Naphthalenes

    This page was last edited on 8 November 2022, at 19:45 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  8. Organosodium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosodium_chemistry

    Organosodium chemistry is the chemistry of organometallic compounds containing a carbon to sodium chemical bond. [1] [2] The application of organosodium compounds in chemistry is limited in part due to competition from organolithium compounds, which are commercially available and exhibit more convenient reactivity.

  9. Alkylated naphthalene - Wikipedia

    en.wikipedia.org/wiki/Alkylated_naphthalene

    Alkylated naphthalenes are chemical compounds made by the alkylation of naphthalene or its derivatives with an olefin. These compounds are used as synthetic base oils, and are claimed to have improved oxidative stability over some conventional base oils.