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(E)-5-Meth­oxy-2-(o-tolyl­imino­meth­yl)phenol

In the title compound, C(15)H(15)NO(2), the phenol group make dihedral angles of 2.4 (2) and 24.1 (9)° with the imine linkage (–C=N–) and the phenyl group, respectively, and the mol­ecule adopts the enol–imine tautomeric form, so the mol­ecular structure is stabilized by a strong intra­molecular O—H...

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Detalles Bibliográficos
Autores principales: Albayrak, Çiğdem, Koşar, Başak, Özek, Arzu, Odabaşoğlu, Mustafa, Büyükgüngör, Orhan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979691/
https://www.ncbi.nlm.nih.gov/pubmed/21579742
http://dx.doi.org/10.1107/S1600536809055615
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author Albayrak, Çiğdem
Koşar, Başak
Özek, Arzu
Odabaşoğlu, Mustafa
Büyükgüngör, Orhan
author_facet Albayrak, Çiğdem
Koşar, Başak
Özek, Arzu
Odabaşoğlu, Mustafa
Büyükgüngör, Orhan
author_sort Albayrak, Çiğdem
collection PubMed
description In the title compound, C(15)H(15)NO(2), the phenol group make dihedral angles of 2.4 (2) and 24.1 (9)° with the imine linkage (–C=N–) and the phenyl group, respectively, and the mol­ecule adopts the enol–imine tautomeric form, so the mol­ecular structure is stabilized by a strong intra­molecular O—H⋯N hydrogen bond. The crystal structure features a weak C—H⋯π inter­action.
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spelling pubmed-29796912010-12-30 (E)-5-Meth­oxy-2-(o-tolyl­imino­meth­yl)phenol Albayrak, Çiğdem Koşar, Başak Özek, Arzu Odabaşoğlu, Mustafa Büyükgüngör, Orhan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(15)NO(2), the phenol group make dihedral angles of 2.4 (2) and 24.1 (9)° with the imine linkage (–C=N–) and the phenyl group, respectively, and the mol­ecule adopts the enol–imine tautomeric form, so the mol­ecular structure is stabilized by a strong intra­molecular O—H⋯N hydrogen bond. The crystal structure features a weak C—H⋯π inter­action. International Union of Crystallography 2010-01-09 /pmc/articles/PMC2979691/ /pubmed/21579742 http://dx.doi.org/10.1107/S1600536809055615 Text en © Albayrak et al. 2010 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
Albayrak, Çiğdem
Koşar, Başak
Özek, Arzu
Odabaşoğlu, Mustafa
Büyükgüngör, Orhan
(E)-5-Meth­oxy-2-(o-tolyl­imino­meth­yl)phenol
title (E)-5-Meth­oxy-2-(o-tolyl­imino­meth­yl)phenol
title_full (E)-5-Meth­oxy-2-(o-tolyl­imino­meth­yl)phenol
title_fullStr (E)-5-Meth­oxy-2-(o-tolyl­imino­meth­yl)phenol
title_full_unstemmed (E)-5-Meth­oxy-2-(o-tolyl­imino­meth­yl)phenol
title_short (E)-5-Meth­oxy-2-(o-tolyl­imino­meth­yl)phenol
title_sort (e)-5-meth­oxy-2-(o-tolyl­imino­meth­yl)phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979691/
https://www.ncbi.nlm.nih.gov/pubmed/21579742
http://dx.doi.org/10.1107/S1600536809055615
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