The oxidative intermolecular cyclocondensation of 3,4-diaminofurazan and 4 , 4 ′-diamino- 3 , 3 ′-azofurazan has been carried out by treating them with mixtures of Pb(OAc) 4 and Bu 4 NBr, Br 2 or NaBr to give previously unknown macrocyclic compounds: polydiazenofurazans possessing differing numbers of units.

We have established the formation of a tetradiazenofurazan macrocycle as a result of intramolecular oxidative cyclization of 4,4′-bis(4-aminofurazanyl-3-azo)-3,3′-azofurazan and have studied its crystal structure.

The oxidative cyclocondensation of 3,4-diaminofurazan and 4,4′-diamino-3,3′-azofurazan with dibromoisocyanurate afforded macrocyclec polydiazenofurazans. The reaction can be directed towards the formation of both the four-membered cycle alone or the three-, six-, and eight-membered macrocycles.

4,4′-Diamino-3,3′-azofurazane undergoes intramolecular oxidative cyclization to give 5-[4-amino(1,2,5)oxadiazolyl]-5H-[1,2,3]triazolo[4,5-c][1,2,5]oxadiazole upon heating with Pb(OAc)4 in chlorobenzene oro-dichlorobenzene or with thionyl chloride.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.