4,4′,6,6′-Tetra­chloro-2,2′-[(1E,1′E)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol

The title compound, C(17)H(14)Cl(4)N(2)O(2), is generated by crystallographic twofold symmetry. The two benzene rings are inclined to one another by 80.17 (10)°. There are two intra­molecular O—H⋯N hydrogen bonds, which make S(6) ring motifs. In the crystal, mol­ecules are linked by C—H⋯O and weak C...

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Detalles Bibliográficos
Autores principales: Kargar, Hadi, Kia, Reza, Adabi Ardakani, Amir, Tahir, Muhammad Nawaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414188/
https://www.ncbi.nlm.nih.gov/pubmed/22904795
http://dx.doi.org/10.1107/S1600536812029443
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author Kargar, Hadi
Kia, Reza
Adabi Ardakani, Amir
Tahir, Muhammad Nawaz
author_facet Kargar, Hadi
Kia, Reza
Adabi Ardakani, Amir
Tahir, Muhammad Nawaz
author_sort Kargar, Hadi
collection PubMed
description The title compound, C(17)H(14)Cl(4)N(2)O(2), is generated by crystallographic twofold symmetry. The two benzene rings are inclined to one another by 80.17 (10)°. There are two intra­molecular O—H⋯N hydrogen bonds, which make S(6) ring motifs. In the crystal, mol­ecules are linked by C—H⋯O and weak C—H⋯Cl inter­actions, forming a three-dimensional network.
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spelling pubmed-34141882012-08-17 4,4′,6,6′-Tetra­chloro-2,2′-[(1E,1′E)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol Kargar, Hadi Kia, Reza Adabi Ardakani, Amir Tahir, Muhammad Nawaz Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(17)H(14)Cl(4)N(2)O(2), is generated by crystallographic twofold symmetry. The two benzene rings are inclined to one another by 80.17 (10)°. There are two intra­molecular O—H⋯N hydrogen bonds, which make S(6) ring motifs. In the crystal, mol­ecules are linked by C—H⋯O and weak C—H⋯Cl inter­actions, forming a three-dimensional network. International Union of Crystallography 2012-07-04 /pmc/articles/PMC3414188/ /pubmed/22904795 http://dx.doi.org/10.1107/S1600536812029443 Text en © Kargar et al. 2012 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
Kargar, Hadi
Kia, Reza
Adabi Ardakani, Amir
Tahir, Muhammad Nawaz
4,4′,6,6′-Tetra­chloro-2,2′-[(1E,1′E)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol
title 4,4′,6,6′-Tetra­chloro-2,2′-[(1E,1′E)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol
title_full 4,4′,6,6′-Tetra­chloro-2,2′-[(1E,1′E)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol
title_fullStr 4,4′,6,6′-Tetra­chloro-2,2′-[(1E,1′E)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol
title_full_unstemmed 4,4′,6,6′-Tetra­chloro-2,2′-[(1E,1′E)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol
title_short 4,4′,6,6′-Tetra­chloro-2,2′-[(1E,1′E)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol
title_sort 4,4′,6,6′-tetra­chloro-2,2′-[(1e,1′e)-propane-1,3-diylbis(nitrilo­methanylyl­idene)]diphenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414188/
https://www.ncbi.nlm.nih.gov/pubmed/22904795
http://dx.doi.org/10.1107/S1600536812029443
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