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  2. Diazonium compound - Wikipedia

    en.wikipedia.org/wiki/Diazonium_compound

    The reaction of the surface with a solution of diazonium salt in acetonitrile for 2 hours in the dark is a spontaneous process through a free radical mechanism: [42] Diazonium salt application silicon wafer. So far grafting of diazonium salts on metals has been accomplished on iron, cobalt, nickel, platinum, palladium, zinc, copper and gold ...

  3. Benzenediazonium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Benzenediazonium_tetrafluo...

    The tetrafluoroborate can be obtained from crude benzenediazonium chloride by salt metathesis using tetrafluoroboric acid. [C 6 H 5 N 2]Cl + HBF 4 → [C 6 H 5 N 2]BF 4 + HCl. The tetrafluoroborate is more stable than the chloride. [2]

  4. Formazan - Wikipedia

    en.wikipedia.org/wiki/Formazan

    Another form to synthesize formazans is by the reaction of active methylene compounds with diazonium salts. Diazonium salts add to active methylene compounds to form an intermediate azo compound, followed by the addition of a second diazonium salt (under more alkaline conditions), yielding tetrazene , which then forms a 3-substituted formazan.

  5. Azo coupling - Wikipedia

    en.wikipedia.org/wiki/Azo_coupling

    In organic chemistry, an azo coupling is an reaction between a diazonium compound (R−N≡N +) and another aromatic compound that produces an azo compound (R−N=N−R’).In this electrophilic aromatic substitution reaction, the aryldiazonium cation is the electrophile, and the activated carbon (usually from an arene, which is called coupling agent), serves as a nucleophile.

  6. Talk:Diazonium compound - Wikipedia

    en.wikipedia.org/wiki/Talk:Diazonium_compound

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  7. Frémy's salt - Wikipedia

    en.wikipedia.org/wiki/Frémy's_salt

    Frémy's salt is a chemical compound with the formula (K 4 [ON(SO 3) 2] 2), sometimes written as (K 2 [NO(SO 3) 2]). It is a bright yellowish-brown solid, but its aqueous solutions are bright violet. It is a bright yellowish-brown solid, but its aqueous solutions are bright violet.

  8. Talk:Conversion of diazonium salt to phenol - Wikipedia

    en.wikipedia.org/wiki/Talk:Conversion_of...

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  9. Zeise's salt - Wikipedia

    en.wikipedia.org/wiki/Zeise's_salt

    Zeise's salt was one of the first organometallic compounds to be reported. [6] It was discovered by William Christopher Zeise, a professor at the University of Copenhagen, who prepared this compound in 1830 while investigating the reaction of PtCl 4 with boiling ethanol.