5-{2-[(2-Hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde

The title compound, C(26)H(21)N(3)O(2), is an unsymmetrical tetra­dentate Schiff base ligand. The hydr­oxy group forms an intra­molecular O—H⋯N hydrogen bond with an adjacent N atom. An inter­molecular N—H⋯O hydrogen bond creates centrosymmetric dimers in the crystal packing.

Detalles Bibliográficos
Autores principales: Liu, Ge, Wang, Jianhui, Guo, Liqin, Ruan, Wen-Juan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962098/
https://www.ncbi.nlm.nih.gov/pubmed/21203255
http://dx.doi.org/10.1107/S1600536808021922
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author Liu, Ge
Wang, Jianhui
Guo, Liqin
Ruan, Wen-Juan
author_facet Liu, Ge
Wang, Jianhui
Guo, Liqin
Ruan, Wen-Juan
author_sort Liu, Ge
collection PubMed
description The title compound, C(26)H(21)N(3)O(2), is an unsymmetrical tetra­dentate Schiff base ligand. The hydr­oxy group forms an intra­molecular O—H⋯N hydrogen bond with an adjacent N atom. An inter­molecular N—H⋯O hydrogen bond creates centrosymmetric dimers in the crystal packing.
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spelling pubmed-29620982010-12-30 5-{2-[(2-Hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde Liu, Ge Wang, Jianhui Guo, Liqin Ruan, Wen-Juan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(26)H(21)N(3)O(2), is an unsymmetrical tetra­dentate Schiff base ligand. The hydr­oxy group forms an intra­molecular O—H⋯N hydrogen bond with an adjacent N atom. An inter­molecular N—H⋯O hydrogen bond creates centrosymmetric dimers in the crystal packing. International Union of Crystallography 2008-07-19 /pmc/articles/PMC2962098/ /pubmed/21203255 http://dx.doi.org/10.1107/S1600536808021922 Text en © Liu et al. 2008 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
Liu, Ge
Wang, Jianhui
Guo, Liqin
Ruan, Wen-Juan
5-{2-[(2-Hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde
title 5-{2-[(2-Hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde
title_full 5-{2-[(2-Hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde
title_fullStr 5-{2-[(2-Hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde
title_full_unstemmed 5-{2-[(2-Hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde
title_short 5-{2-[(2-Hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde
title_sort 5-{2-[(2-hydroxy-5-methyl­phen­yl)(phenyl)methyl­eneamino]phenyl­imino­meth­yl}­pyrrole-2-carbaldehyde
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962098/
https://www.ncbi.nlm.nih.gov/pubmed/21203255
http://dx.doi.org/10.1107/S1600536808021922
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AT guoliqin 522hydroxy5methylphenylphenylmethyleneaminophenyliminomethylpyrrole2carbaldehyde
AT ruanwenjuan 522hydroxy5methylphenylphenylmethyleneaminophenyliminomethylpyrrole2carbaldehyde

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