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Syntheses, spectroscopy, and crystal structures of 3-(4-bromo­phen­yl)-1,5-di­phenyl­formazan and the 3-(4-bromo­phen­yl)-1,5-di­phenyl­verdazyl radical and the crystal structure of the by-product 5-anilino-3-(4-bromo­phen­yl)-1-phenyl-1H-1,2,4-triazole

The title compounds, C(19)H(15)BrN(4), C(20)H(16)BrN(4) and C(20)H(15)BrN(4), are nitro­gen-rich organic compounds that are related by their synthesis. The verdazyl radical, in which stacking leads to anti­ferromagnetic inter­actions, was reported previously [Iwase et al. (2013 ▸). Phys. Rev. B, 88,...

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Detalles Bibliográficos
Autores principales: Schnakenburg, Gregor, Meyer, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947789/
https://www.ncbi.nlm.nih.gov/pubmed/29765709
http://dx.doi.org/10.1107/S2056989018001913
Descripción
Sumario:The title compounds, C(19)H(15)BrN(4), C(20)H(16)BrN(4) and C(20)H(15)BrN(4), are nitro­gen-rich organic compounds that are related by their synthesis. The verdazyl radical, in which stacking leads to anti­ferromagnetic inter­actions, was reported previously [Iwase et al. (2013 ▸). Phys. Rev. B, 88, 184431]. For this compound, improved structural data and spectroscopic data are presented. The other two compounds have been crystallized for the first time and form stacks of dimers, roughly along the a-axis direction of the crystal. The formazan mol­ecule shows signs of rapid intra­molecular H-atom exchange typical for this class of compounds and spectroscopic data are provided in addition to the crystal structure. The triazole compound appears to be a side-product of the verdazyl synthesis.