2-[(E)-(5-Amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol

The title Schiff base compound, C(27)H(19)ClN(4)O, features two intra­molecular O—H⋯N and N—H⋯N hydrogen bonds involving the hydr­oxy and amino groups to generate S(6) and S(5) ring motifs, respectively. In the crystal structure, weak inter­molecular N—H⋯O and C—H⋯N inter­actions, together with π–π...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Kia, Reza, Raithby, Paul R.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962046/
https://www.ncbi.nlm.nih.gov/pubmed/21203131
http://dx.doi.org/10.1107/S1600536808020023
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author Fun, Hoong-Kun
Kia, Reza
Raithby, Paul R.
author_facet Fun, Hoong-Kun
Kia, Reza
Raithby, Paul R.
author_sort Fun, Hoong-Kun
collection PubMed
description The title Schiff base compound, C(27)H(19)ClN(4)O, features two intra­molecular O—H⋯N and N—H⋯N hydrogen bonds involving the hydr­oxy and amino groups to generate S(6) and S(5) ring motifs, respectively. In the crystal structure, weak inter­molecular N—H⋯O and C—H⋯N inter­actions, together with π–π contacts [centroid–centroid distances = 3.6294 (11)–3.6881 (11) Å], link neighboring mol­ecules.
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spelling pubmed-29620462010-12-30 2-[(E)-(5-Amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol Fun, Hoong-Kun Kia, Reza Raithby, Paul R. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title Schiff base compound, C(27)H(19)ClN(4)O, features two intra­molecular O—H⋯N and N—H⋯N hydrogen bonds involving the hydr­oxy and amino groups to generate S(6) and S(5) ring motifs, respectively. In the crystal structure, weak inter­molecular N—H⋯O and C—H⋯N inter­actions, together with π–π contacts [centroid–centroid distances = 3.6294 (11)–3.6881 (11) Å], link neighboring mol­ecules. International Union of Crystallography 2008-07-05 /pmc/articles/PMC2962046/ /pubmed/21203131 http://dx.doi.org/10.1107/S1600536808020023 Text en © Fun 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
Fun, Hoong-Kun
Kia, Reza
Raithby, Paul R.
2-[(E)-(5-Amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol
title 2-[(E)-(5-Amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol
title_full 2-[(E)-(5-Amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol
title_fullStr 2-[(E)-(5-Amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol
title_full_unstemmed 2-[(E)-(5-Amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol
title_short 2-[(E)-(5-Amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol
title_sort 2-[(e)-(5-amino-2,3-diphenyl­quinoxalin-6-yl)imino­meth­yl]-4-chloro­phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962046/
https://www.ncbi.nlm.nih.gov/pubmed/21203131
http://dx.doi.org/10.1107/S1600536808020023
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AT raithbypaulr 2e5amino23diphenylquinoxalin6yliminomethyl4chlorophenol

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