4,4′,6,6′-Tetra­bromo-2,2′-[(E,E)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol

The asymmetric unit of the title compound, C(16)H(12)Br(4)N(2)O(2), comprises half of a potential tetra­dentate Schiff base ligand. The whole mol­ecule is generated by an inversion center located in the middle of the C—C bond of the ethyl­ene segment. There are intra­molecular O—H⋯N hydrogen bonds m...

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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/PMC3414283/
https://www.ncbi.nlm.nih.gov/pubmed/22904816
http://dx.doi.org/10.1107/S1600536812029832
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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 asymmetric unit of the title compound, C(16)H(12)Br(4)N(2)O(2), comprises half of a potential tetra­dentate Schiff base ligand. The whole mol­ecule is generated by an inversion center located in the middle of the C—C bond of the ethyl­ene segment. There are intra­molecular O—H⋯N hydrogen bonds making S(6) ring motifs. In the crystal, no significant inter­molecular inter­actions are observed.
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spelling pubmed-34142832012-08-17 4,4′,6,6′-Tetra­bromo-2,2′-[(E,E)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol Kargar, Hadi Kia, Reza Adabi Ardakani, Amir Tahir, Muhammad Nawaz Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(16)H(12)Br(4)N(2)O(2), comprises half of a potential tetra­dentate Schiff base ligand. The whole mol­ecule is generated by an inversion center located in the middle of the C—C bond of the ethyl­ene segment. There are intra­molecular O—H⋯N hydrogen bonds making S(6) ring motifs. In the crystal, no significant inter­molecular inter­actions are observed. International Union of Crystallography 2012-07-07 /pmc/articles/PMC3414283/ /pubmed/22904816 http://dx.doi.org/10.1107/S1600536812029832 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′-Tetra­bromo-2,2′-[(E,E)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol
title 4,4′,6,6′-Tetra­bromo-2,2′-[(E,E)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol
title_full 4,4′,6,6′-Tetra­bromo-2,2′-[(E,E)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol
title_fullStr 4,4′,6,6′-Tetra­bromo-2,2′-[(E,E)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol
title_full_unstemmed 4,4′,6,6′-Tetra­bromo-2,2′-[(E,E)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol
title_short 4,4′,6,6′-Tetra­bromo-2,2′-[(E,E)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol
title_sort 4,4′,6,6′-tetra­bromo-2,2′-[(e,e)-ethane-1,2-diylbis(nitrilo­methanylyl­idene)]di­phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414283/
https://www.ncbi.nlm.nih.gov/pubmed/22904816
http://dx.doi.org/10.1107/S1600536812029832
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