 | This is the sandbox page where you will draft your initial Wikipedia contribution.
If you're starting a new article, you can develop it here until it's ready to go live. If you're working on improvements to an existing article, copy only one section at a time of the article to this sandbox to work on, and be sure to use an edit summary linking to the article you copied from. Do not copy over the entire article. You can find additional instructions here. Remember to save your work regularly using the "Publish page" button. (It just means 'save'; it will still be in the sandbox.) You can add bold formatting to your additions to differentiate them from existing content. |
Azo Coupling
editIn organic chemistry, an azo coupling is an organic 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) acts as a nucleophile.[1] The desired azo compound is synthesized from this para substitution reaction. In most cases, including the examples below, the diazonium compound is also aromatic.
Diazotization
editThe process of converting primary aromatic amines into its diazonium salt is called diazotization. Diazonium salts are important synthetic intermediates that can undergo coupling reactions to form azo dyes and electrophilic substitution reactions to introduce functional groups. The azo product is obtained upon acidic workup.
Uses of the reaction
editAromatic azo compounds tend to be brightly colored due to the extended conjugated systems. Many are used as dyes (see azo dye).[2] Important azo dyes include methyl red and pigment red 170. Azo printing exploits this reaction as well. In this case, the diazonium ion is degraded by light, leaving a latent image in undegraded diazonium salt which is made to react with a phenol, producing a colored image: the blueprint.[3]
Prontosil, a first sulfa drug, was once produced by azo coupling. The azo compound is a prodrug that is activated in-vivo to produce the sufanilamide, which is active.
The reaction is also used in the Pauly reaction test to detect tyrosine or histidine residues in proteins.
Examples of azo C-coupling reactions
editMany procedures have been described, which re.[4][5] Phenol reacts with benzenediazonium chloride to give a Solvent Yellow 7, a yellow-orange azo compound. The reaction is faster at high pH.[6]
The related dye called aniline yellow is produced from the reaction of aniline and the diazonium salt. In this case the C- and N-coupling compete.[6] When the para position (the Carbon directly opposing to the R-group) is substituted for aromatic electrophilic substitution, coupling occurs at the ortho position (one of the two Carbons closest to the R-group), albeit at a slower rate.
Naphthols are popular coupling agents. One example is the synthesis of the dye "organol brown" from aniline and 1-naphthol:
Similarly β-naphthol couples with phenyldiazonium electrophile to produce an intense orange-red dye.
Besides activated carbons in aromatic rings, other nucleophilic carbons could also be coupled with diazonium salt:
Examples of azo N-coupling reactions
edit
In alkaline media, diazonium salt can react with most primary and secondary amines that exist as a free base and produce triazene.[7] This chemical reaction is called azo N-coupling[8] or the synthesis of azoamines.[9]
References
edit- ^ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1
- ^ Klaus Hunger; Peter Mischke; Wolfgang Rieper; Roderich Raue; Klaus Kunde; Aloys Engel (2005). "Azo Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_245. ISBN 978-3527306732.
- ^ Pai, Damodar M.; Melnyk, Andrew R.; Weiss, David S.; Hann, Richard; Crooks, Walter; Pennington, Keith S.; Lee, Francis C.; Jaeger, C. Wayne; Titterington, Don R.; Lutz, Walter; Bräuninger, Arno; De Brabandere, Luc; Claes, Frans; De Keyzer, Rene; Janssens, Wilhelmus; Potts, Rod. "Imaging Technology, 2. Copying and Nonimpact Printing Processes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. pp. 1–53. doi:10.1002/14356007.o13_o08.pub2. ISBN 9783527306732.
- ^ J. L. Hartwell and Louis F. Fieser. "Coupling of o-tolidine and Chicago acid". Organic Syntheses; Collected Volumes, vol. 2, p. 145.
- ^ H. T. Clarke and W. R. Kirner. "Methyl red". Organic Syntheses; Collected Volumes, vol. 1, p. 374.
- ^ a b Klaus Hunger; Peter Mischke; Wolfgang Rieper; Roderich Raue; Klaus Kunde; Aloys Engel (2005). "Azo Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_245. ISBN 978-3527306732.
- ^ Khazaei; et al. (2012). "azo amine coupling giving triazenes, and triazene's decomposition giving diazonium salt". Synlett. 23 (13): 1893–1896. doi:10.1055/s-0032-1316557. S2CID 196805424.
- ^ Wiley Subscription Services (2013). "Synthesis, characterization, and application of a triazene-base polymer". Journal of Applied Polymer Science. 129 (6): 3439–3446. doi:10.1002/app.39069.
- ^ Serge Ratton, Bernard Botannet (1981). "Preparation of aromatic azoamines by diazotization/coupling/rearrangement of aromatic amines". US Patent 4275003A.