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(E)-2-[2-(3-Nitro­phen­yl)ethen­yl]quinolin-8-ol

In the title compound, C(17)H(12)N(2)O(3), the mean planes of the benzene ring and the quinoline moiety are inclined to one another by 11.0 (1)°. The nitro substituent is twisted at an angle of 7.9 (2)° with respect to the attached benzene ring. Intra­molecular O—H⋯N and C—H⋯N hydrogen bonds occur....

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Detalles Bibliográficos
Autores principales: Schulze, Mathias, Seichter, Wilhelm, Weber, Edwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884316/
https://www.ncbi.nlm.nih.gov/pubmed/24454092
http://dx.doi.org/10.1107/S1600536813027815
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author Schulze, Mathias
Seichter, Wilhelm
Weber, Edwin
author_facet Schulze, Mathias
Seichter, Wilhelm
Weber, Edwin
author_sort Schulze, Mathias
collection PubMed
description In the title compound, C(17)H(12)N(2)O(3), the mean planes of the benzene ring and the quinoline moiety are inclined to one another by 11.0 (1)°. The nitro substituent is twisted at an angle of 7.9 (2)° with respect to the attached benzene ring. Intra­molecular O—H⋯N and C—H⋯N hydrogen bonds occur. The crystal is constructed of mol­ecular stacks without involvement of π-stacking inter­actions, but showing inter­stack association via O—H⋯O and C—H⋯O hydrogen bonding. Thus, the supramolecular architecture of the crystal results from stacked molecules stabilized by hydrogen bonding between the stacks.
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spelling pubmed-38843162014-01-17 (E)-2-[2-(3-Nitro­phen­yl)ethen­yl]quinolin-8-ol Schulze, Mathias Seichter, Wilhelm Weber, Edwin Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(12)N(2)O(3), the mean planes of the benzene ring and the quinoline moiety are inclined to one another by 11.0 (1)°. The nitro substituent is twisted at an angle of 7.9 (2)° with respect to the attached benzene ring. Intra­molecular O—H⋯N and C—H⋯N hydrogen bonds occur. The crystal is constructed of mol­ecular stacks without involvement of π-stacking inter­actions, but showing inter­stack association via O—H⋯O and C—H⋯O hydrogen bonding. Thus, the supramolecular architecture of the crystal results from stacked molecules stabilized by hydrogen bonding between the stacks. International Union of Crystallography 2013-10-16 /pmc/articles/PMC3884316/ /pubmed/24454092 http://dx.doi.org/10.1107/S1600536813027815 Text en © Schulze 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
Schulze, Mathias
Seichter, Wilhelm
Weber, Edwin
(E)-2-[2-(3-Nitro­phen­yl)ethen­yl]quinolin-8-ol
title (E)-2-[2-(3-Nitro­phen­yl)ethen­yl]quinolin-8-ol
title_full (E)-2-[2-(3-Nitro­phen­yl)ethen­yl]quinolin-8-ol
title_fullStr (E)-2-[2-(3-Nitro­phen­yl)ethen­yl]quinolin-8-ol
title_full_unstemmed (E)-2-[2-(3-Nitro­phen­yl)ethen­yl]quinolin-8-ol
title_short (E)-2-[2-(3-Nitro­phen­yl)ethen­yl]quinolin-8-ol
title_sort (e)-2-[2-(3-nitro­phen­yl)ethen­yl]quinolin-8-ol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884316/
https://www.ncbi.nlm.nih.gov/pubmed/24454092
http://dx.doi.org/10.1107/S1600536813027815
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