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dc.contributor.authorDolzhenko, Anton
dc.contributor.authorTan, G.
dc.contributor.authorKoh, L.
dc.contributor.authorDolzhenko, A.
dc.contributor.authorChui, W.
dc.date.accessioned2017-01-30T14:20:00Z
dc.date.available2017-01-30T14:20:00Z
dc.date.created2011-08-22T20:01:17Z
dc.date.issued2009
dc.identifier.citationDolzhenko, A.V. and Tan, G.K. and Koh, L.L. and Dolzhenko, A.V. and Chui, W.K. 2009. 3-Phenyl-1H-1,2,4-triazol-5-amine-5-phenyl-1H-1,2,4-triazol-3-amine (1/1). Acta Crystallographica Section E - Structure Reports Online. E65 (1): o126.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/38394
dc.identifier.doi10.1107/S1600536808042165
dc.description.abstract

In the title compound, C8H8N4-C8H8N4, two tautomers, viz. 3-phenyl-1,2,4-triazol-5-amine and 5-phenyl-1,2,4-triazol-3-amine, are crystallized together in equal amounts. The 3-phenyl-1,2,4-triazol-5-amine molecule is essentially planar; the phenyl ring makes a dihedral angle of 2.3 (2)degrees with the mean plane of the 1,2,4-triazole ring. In the 5-phenyl-1,2,4-triazol-3-amine tautomer, the mean planes of the phenyl and 1,2,4-triazole rings form a dihedral angle of 30.8 (2)degrees. The electron delocalization of the amino group with the 1,2,4-triazole nucleus in the 3-phenyl-1,2,4-triazol-5-amine molecule is more extensive than that in the 5-phenyl-1,2,4-triazol-3-amine tautomer. The molecules are linked into a two-dimensional network parallel to (100) by N-H...N hydrogen bonds.

dc.publisherBlackwell Munksgaard
dc.title3-Phenyl-1H-1,2,4-triazol-5-amine-5-phenyl-1H-1,2,4-triazol-3-amine (1/1).
dc.typeJournal Article
dcterms.source.volumeE65
dcterms.source.number1
dcterms.source.issn16005368
dcterms.source.titleActa Crystallographica Section E - Structure Reports Online
curtin.note

This open-access article is distributed under the terms of the Creative Commons Attribution Licence http://creativecommons.org/licenses/by/2.0/uk/legalcode, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

curtin.departmentSchool of Pharmacy
curtin.accessStatusOpen access


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