(E)-1-[(2,4,6-Tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol

The title azo mol­ecule, C(16)H(9)Br(3)N(2)O, adopts a trans conformation with respect to the azo N=N double bond. An intra­molecular O—H⋯N hydrogen bond forms an S(6) ring motif. The dihedral angle between the naphthalene ring system and the benzene ring is 33.80 (16)°. In the crystal, mol­ecules a...

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Detalles Bibliográficos
Autores principales: Chetioui, Souheyla, Boudraa, Issam, Bouacida, Sofiane, Bouchoul, Abdelkader, Bouaoud, Salah Eddine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793751/
https://www.ncbi.nlm.nih.gov/pubmed/24109338
http://dx.doi.org/10.1107/S1600536813018977
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author Chetioui, Souheyla
Boudraa, Issam
Bouacida, Sofiane
Bouchoul, Abdelkader
Bouaoud, Salah Eddine
author_facet Chetioui, Souheyla
Boudraa, Issam
Bouacida, Sofiane
Bouchoul, Abdelkader
Bouaoud, Salah Eddine
author_sort Chetioui, Souheyla
collection PubMed
description The title azo mol­ecule, C(16)H(9)Br(3)N(2)O, adopts a trans conformation with respect to the azo N=N double bond. An intra­molecular O—H⋯N hydrogen bond forms an S(6) ring motif. The dihedral angle between the naphthalene ring system and the benzene ring is 33.80 (16)°. In the crystal, mol­ecules are stacked in columns along the a axis by π–π inter­actions [centroid–centroid distances = 3.815 (3) and 3.990 (3) Å].
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spelling pubmed-37937512013-10-09 (E)-1-[(2,4,6-Tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol Chetioui, Souheyla Boudraa, Issam Bouacida, Sofiane Bouchoul, Abdelkader Bouaoud, Salah Eddine Acta Crystallogr Sect E Struct Rep Online Organic Papers The title azo mol­ecule, C(16)H(9)Br(3)N(2)O, adopts a trans conformation with respect to the azo N=N double bond. An intra­molecular O—H⋯N hydrogen bond forms an S(6) ring motif. The dihedral angle between the naphthalene ring system and the benzene ring is 33.80 (16)°. In the crystal, mol­ecules are stacked in columns along the a axis by π–π inter­actions [centroid–centroid distances = 3.815 (3) and 3.990 (3) Å]. International Union of Crystallography 2013-07-13 /pmc/articles/PMC3793751/ /pubmed/24109338 http://dx.doi.org/10.1107/S1600536813018977 Text en © Chetioui et al. 2013 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Chetioui, Souheyla
Boudraa, Issam
Bouacida, Sofiane
Bouchoul, Abdelkader
Bouaoud, Salah Eddine
(E)-1-[(2,4,6-Tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol
title (E)-1-[(2,4,6-Tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol
title_full (E)-1-[(2,4,6-Tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol
title_fullStr (E)-1-[(2,4,6-Tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol
title_full_unstemmed (E)-1-[(2,4,6-Tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol
title_short (E)-1-[(2,4,6-Tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol
title_sort (e)-1-[(2,4,6-tri­bromo­phen­yl)diazen­yl]naphthalen-2-ol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793751/
https://www.ncbi.nlm.nih.gov/pubmed/24109338
http://dx.doi.org/10.1107/S1600536813018977
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