2-[(E)-(2,4,6-Trichloro­phen­yl)imino­meth­yl]phenol

The title mol­ecule, C(13)H(8)Cl(3)NO, exists in a trans configuration with respect to the C=N bond [1.278 (2) Å]. The benzene rings form a dihedral angle of 24.64 (11)°. The mol­ecular structure is stabilized by an intra­molecular O—H⋯N hydrogen bond, which generates an S(6) ring motif. In the crys...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Quah, Ching Kheng, Viveka, S., Madhukumar, D. J., Nagaraja, G. K.
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/PMC3212321/
https://www.ncbi.nlm.nih.gov/pubmed/22090978
http://dx.doi.org/10.1107/S1600536811026122
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author Fun, Hoong-Kun
Quah, Ching Kheng
Viveka, S.
Madhukumar, D. J.
Nagaraja, G. K.
author_facet Fun, Hoong-Kun
Quah, Ching Kheng
Viveka, S.
Madhukumar, D. J.
Nagaraja, G. K.
author_sort Fun, Hoong-Kun
collection PubMed
description The title mol­ecule, C(13)H(8)Cl(3)NO, exists in a trans configuration with respect to the C=N bond [1.278 (2) Å]. The benzene rings form a dihedral angle of 24.64 (11)°. The mol­ecular structure is stabilized by an intra­molecular O—H⋯N hydrogen bond, which generates an S(6) ring motif. In the crystal, π–π stacking inter­actions [centroid–centroid distances = 3.6893 (14) Å] are observed.
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spelling pubmed-32123212011-11-16 2-[(E)-(2,4,6-Trichloro­phen­yl)imino­meth­yl]phenol Fun, Hoong-Kun Quah, Ching Kheng Viveka, S. Madhukumar, D. J. Nagaraja, G. K. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title mol­ecule, C(13)H(8)Cl(3)NO, exists in a trans configuration with respect to the C=N bond [1.278 (2) Å]. The benzene rings form a dihedral angle of 24.64 (11)°. The mol­ecular structure is stabilized by an intra­molecular O—H⋯N hydrogen bond, which generates an S(6) ring motif. In the crystal, π–π stacking inter­actions [centroid–centroid distances = 3.6893 (14) Å] are observed. International Union of Crystallography 2011-07-06 /pmc/articles/PMC3212321/ /pubmed/22090978 http://dx.doi.org/10.1107/S1600536811026122 Text en © Fun 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
Fun, Hoong-Kun
Quah, Ching Kheng
Viveka, S.
Madhukumar, D. J.
Nagaraja, G. K.
2-[(E)-(2,4,6-Trichloro­phen­yl)imino­meth­yl]phenol
title 2-[(E)-(2,4,6-Trichloro­phen­yl)imino­meth­yl]phenol
title_full 2-[(E)-(2,4,6-Trichloro­phen­yl)imino­meth­yl]phenol
title_fullStr 2-[(E)-(2,4,6-Trichloro­phen­yl)imino­meth­yl]phenol
title_full_unstemmed 2-[(E)-(2,4,6-Trichloro­phen­yl)imino­meth­yl]phenol
title_short 2-[(E)-(2,4,6-Trichloro­phen­yl)imino­meth­yl]phenol
title_sort 2-[(e)-(2,4,6-trichloro­phen­yl)imino­meth­yl]phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212321/
https://www.ncbi.nlm.nih.gov/pubmed/22090978
http://dx.doi.org/10.1107/S1600536811026122
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AT nagarajagk 2e246trichlorophenyliminomethylphenol

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