అవిభాజ్య కేషన్ r-n:n- (ఇక్కడ r అనేది సుగంధ హైడ్రోకార్బన్,

diazonium's Usage Examples:

In the primary reaction product the intermediate alkyl radical is then captured by the diazonium counterion X which is usually a halogen.

The arene compound 1 (here benzene) is coupled with base with the diazonium salt 2 to the biaryl 3 through.

Meerwein arylation is an organic reaction involving the addition of an aryl diazonium salt (ArN2X) to an electron-poor alkene usually supported by a metal salt.

Allylic alcohols, conjugated alkenes, unsaturated heterocycles and unactivated alkenes are capable of being arylated with arenediazonium salts using.

This genus no longer includes species that test positive to diazonium blue B (DBB).

It is a salt of a diazonium cation and chloride.

The proposed Heck catalytic cycle involving cationic palladium with diazonium salts was reinforced by studies with mass spectrometry (ESI) by Correia.

{H2O}} _{water}}} Amines react with nitrous acid to give diazonium salts.

aryl-aryl coupling reaction via a diazonium salt.

preferred that the diazonium salt remain in solution, but they do tend to supersaturate.

which a primary aromatic amine is transformed to an aryl fluoride via a diazonium tetrafluoroborate intermediate.

Reactions in which proton transfer is rate-determining exhibit general acid catalysis, for example diazonium coupling reactions.

Pigment Yellow 6 (CAS# 2512-29-0), derived from 4-chloro-2-nitroaniline (diazonium precursor) and aniline (acetoacetanilide precursor) to produce medium.