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(E)-2-[(3-Fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol

The title compound, C(14)H(9)F(4)NO(2), is a Schiff base which adopts the phenol–imine tautomeric form in the solid state. The H atom is located on the hydr­oxy O atom rather than on the N atom. This H atom is involved in a strong intra­molecular O—H⋯N hydrogen bond. The mol­ecule is almost planar,...

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Detalles Bibliográficos
Autores principales: Bingöl Alpaslan, Yelda, Alpaslan, Gökhan, Ağar, Ayşen, Işık, Şamil
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983675/
https://www.ncbi.nlm.nih.gov/pubmed/21580285
http://dx.doi.org/10.1107/S1600536810002989
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author Bingöl Alpaslan, Yelda
Alpaslan, Gökhan
Ağar, Ayşen
Işık, Şamil
author_facet Bingöl Alpaslan, Yelda
Alpaslan, Gökhan
Ağar, Ayşen
Işık, Şamil
author_sort Bingöl Alpaslan, Yelda
collection PubMed
description The title compound, C(14)H(9)F(4)NO(2), is a Schiff base which adopts the phenol–imine tautomeric form in the solid state. The H atom is located on the hydr­oxy O atom rather than on the N atom. This H atom is involved in a strong intra­molecular O—H⋯N hydrogen bond. The mol­ecule is almost planar, the angle between the benzene rings being 2.14 (13)°.
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spelling pubmed-29836752010-12-30 (E)-2-[(3-Fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol Bingöl Alpaslan, Yelda Alpaslan, Gökhan Ağar, Ayşen Işık, Şamil Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(9)F(4)NO(2), is a Schiff base which adopts the phenol–imine tautomeric form in the solid state. The H atom is located on the hydr­oxy O atom rather than on the N atom. This H atom is involved in a strong intra­molecular O—H⋯N hydrogen bond. The mol­ecule is almost planar, the angle between the benzene rings being 2.14 (13)°. International Union of Crystallography 2010-02-03 /pmc/articles/PMC2983675/ /pubmed/21580285 http://dx.doi.org/10.1107/S1600536810002989 Text en © Bingöl Alpaslan 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
Bingöl Alpaslan, Yelda
Alpaslan, Gökhan
Ağar, Ayşen
Işık, Şamil
(E)-2-[(3-Fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol
title (E)-2-[(3-Fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol
title_full (E)-2-[(3-Fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol
title_fullStr (E)-2-[(3-Fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol
title_full_unstemmed (E)-2-[(3-Fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol
title_short (E)-2-[(3-Fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol
title_sort (e)-2-[(3-fluoro­phen­yl)imino­meth­yl]-4-(trifluoro­meth­oxy)phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983675/
https://www.ncbi.nlm.nih.gov/pubmed/21580285
http://dx.doi.org/10.1107/S1600536810002989
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