2-Hy­droxy-N-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride

The crystal structure of the title compound, C(14)H(15)N(2)O(4) (+)·Cl(−), can be described as being composed of layers containing both cations and anions that are staggered along [010]. Two types of the hydrogen bonds are observed, viz. cation–anion and cation–cation. The chloride anions are accept...

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Detalles Bibliográficos
Autores principales: Boulcina, Raouf, Fantazi, Boubakeur, Bouacida, Sofiane, Roisnel, Thierry, Debache, Abdelmadjid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213600/
https://www.ncbi.nlm.nih.gov/pubmed/22091177
http://dx.doi.org/10.1107/S1600536811029552
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author Boulcina, Raouf
Fantazi, Boubakeur
Bouacida, Sofiane
Roisnel, Thierry
Debache, Abdelmadjid
author_facet Boulcina, Raouf
Fantazi, Boubakeur
Bouacida, Sofiane
Roisnel, Thierry
Debache, Abdelmadjid
author_sort Boulcina, Raouf
collection PubMed
description The crystal structure of the title compound, C(14)H(15)N(2)O(4) (+)·Cl(−), can be described as being composed of layers containing both cations and anions that are staggered along [010]. Two types of the hydrogen bonds are observed, viz. cation–anion and cation–cation. The chloride anions are acceptors of the strong hydrogen bonds donated by the secondary amine and the hy­droxy groups. The packing is also stabilized by weak C—H⋯O inter­molecular hydrogen bonds. An intra­molecular N—H⋯O inter­action also occurs.
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spelling pubmed-32136002011-11-16 2-Hy­droxy-N-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride Boulcina, Raouf Fantazi, Boubakeur Bouacida, Sofiane Roisnel, Thierry Debache, Abdelmadjid Acta Crystallogr Sect E Struct Rep Online Organic Papers The crystal structure of the title compound, C(14)H(15)N(2)O(4) (+)·Cl(−), can be described as being composed of layers containing both cations and anions that are staggered along [010]. Two types of the hydrogen bonds are observed, viz. cation–anion and cation–cation. The chloride anions are acceptors of the strong hydrogen bonds donated by the secondary amine and the hy­droxy groups. The packing is also stabilized by weak C—H⋯O inter­molecular hydrogen bonds. An intra­molecular N—H⋯O inter­action also occurs. International Union of Crystallography 2011-07-30 /pmc/articles/PMC3213600/ /pubmed/22091177 http://dx.doi.org/10.1107/S1600536811029552 Text en © Boulcina et al. 2011 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
Boulcina, Raouf
Fantazi, Boubakeur
Bouacida, Sofiane
Roisnel, Thierry
Debache, Abdelmadjid
2-Hy­droxy-N-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride
title 2-Hy­droxy-N-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride
title_full 2-Hy­droxy-N-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride
title_fullStr 2-Hy­droxy-N-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride
title_full_unstemmed 2-Hy­droxy-N-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride
title_short 2-Hy­droxy-N-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride
title_sort 2-hy­droxy-n-(4-meth­oxy­benz­yl)-4-nitro­anilinium chloride
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213600/
https://www.ncbi.nlm.nih.gov/pubmed/22091177
http://dx.doi.org/10.1107/S1600536811029552
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