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Mu1,3-azido-diazidotetrakis(1,10-phenanthroline)dicopper(II) azide tetrahydrate

Ya-Qian Cheng1, Mao-Lin Hu, Shun Wang

  • 1Department of Chemistry, Wenzhou Normal College, Wenzhou, 325027, People's Republic of China. hu1964615@263.net

Acta Crystallographica. Section C, Crystal Structure Communications
|January 10, 2002
PubMed

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The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para position.