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Crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine

In the title biphenyl derivative, C(12)H(9)N(3)O(4), the dihedral angle between the benzene rings is 52.84 (10)°. The nitro group attached to the benzene ring is inclined to the ring by 4.03 (2)°, while the nitro group attached to the amino-substituted benzene ring is inclined to the ring by 8.84 (2...

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Autores principales: Faizi, Md. Serajul Haque, Haque, Ashanul, Dege, Necmi, Hasan, Syed Imran, Dege, Mustafa, Kalibabchuk, Valentina A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382619/
https://www.ncbi.nlm.nih.gov/pubmed/28435718
http://dx.doi.org/10.1107/S205698901700408X
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author Faizi, Md. Serajul Haque
Haque, Ashanul
Dege, Necmi
Hasan, Syed Imran
Dege, Mustafa
Kalibabchuk, Valentina A.
author_facet Faizi, Md. Serajul Haque
Haque, Ashanul
Dege, Necmi
Hasan, Syed Imran
Dege, Mustafa
Kalibabchuk, Valentina A.
author_sort Faizi, Md. Serajul Haque
collection PubMed
description In the title biphenyl derivative, C(12)H(9)N(3)O(4), the dihedral angle between the benzene rings is 52.84 (10)°. The nitro group attached to the benzene ring is inclined to the ring by 4.03 (2)°, while the nitro group attached to the amino-substituted benzene ring is inclined to the ring by 8.84 (2)°. In the crystal, mol­ecules are linked by two pairs of N—H⋯O hydrogen bonds, forming chains propagating along [101]. Within the chains, these N—H⋯O hydrogen bonds result in the formation of R (2) (2)(20) and R (2) (2)(14) ring motifs. The latter ring motif is reinforced by a pair of C—H⋯O hydrogen bonds, enclosing R (2) (1)(6) ring motifs. The chains are linked by a second C—H⋯O hydrogen bond, forming a three-dimensional supra­molecular structure.
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spelling pubmed-53826192017-04-21 Crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine Faizi, Md. Serajul Haque Haque, Ashanul Dege, Necmi Hasan, Syed Imran Dege, Mustafa Kalibabchuk, Valentina A. Acta Crystallogr E Crystallogr Commun Research Communications In the title biphenyl derivative, C(12)H(9)N(3)O(4), the dihedral angle between the benzene rings is 52.84 (10)°. The nitro group attached to the benzene ring is inclined to the ring by 4.03 (2)°, while the nitro group attached to the amino-substituted benzene ring is inclined to the ring by 8.84 (2)°. In the crystal, mol­ecules are linked by two pairs of N—H⋯O hydrogen bonds, forming chains propagating along [101]. Within the chains, these N—H⋯O hydrogen bonds result in the formation of R (2) (2)(20) and R (2) (2)(14) ring motifs. The latter ring motif is reinforced by a pair of C—H⋯O hydrogen bonds, enclosing R (2) (1)(6) ring motifs. The chains are linked by a second C—H⋯O hydrogen bond, forming a three-dimensional supra­molecular structure. International Union of Crystallography 2017-03-21 /pmc/articles/PMC5382619/ /pubmed/28435718 http://dx.doi.org/10.1107/S205698901700408X Text en © Faizi et al. 2017 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/2.0/uk/
spellingShingle Research Communications
Faizi, Md. Serajul Haque
Haque, Ashanul
Dege, Necmi
Hasan, Syed Imran
Dege, Mustafa
Kalibabchuk, Valentina A.
Crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine
title Crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine
title_full Crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine
title_fullStr Crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine
title_full_unstemmed Crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine
title_short Crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine
title_sort crystal structure of 4,4′-di­nitro-[1,1′-biphen­yl]-2-amine
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382619/
https://www.ncbi.nlm.nih.gov/pubmed/28435718
http://dx.doi.org/10.1107/S205698901700408X
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