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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. Surface treatment of PTFE - Wikipedia

    en.wikipedia.org/wiki/Surface_treatment_of_PTFE

    The fluorine-to-carbon atomic ratio (F/C ratio) is reduced from PTFE's theoretical ratio of 2.0 to 0.2 or less, after exposure to sodium naphthalene for 1 minute. [ 6 ] [ 7 ] [ 8 ] The fluorine atoms are replaced with hydroxyl, carbonyl, and other functional groups which can form hydrogen bonds.

  5. Anionic addition polymerization - Wikipedia

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

    Vinyl monomers have the formula CH 2 =CHR, the most important are styrene (R = C 6 H 5), butadiene (R = CH=CH 2), and isoprene (R = C(Me)=CH 2). A second major class of monomers are acrylate esters, such as acrylonitrile, methacrylate, cyanoacrylate, and acrolein. Other vinyl monomers include vinylpyridine, vinyl sulfone, vinyl sulfoxide, vinyl ...

  6. 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.

  7. Category:Naphthalenes - Wikipedia

    en.wikipedia.org/wiki/Category:Naphthalenes

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  8. Sodium compounds - Wikipedia

    en.wikipedia.org/wiki/Sodium_compounds

    Sodium atoms have 11 electrons, one more than the stable configuration of the noble gas neon. As a result, sodium usually forms ionic compounds involving the Na + cation. [1] Sodium is a reactive alkali metal and is much more stable in ionic compounds. It can also form intermetallic compounds and organosodium compounds.

  9. 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.