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2,2′-[(E,E)-cis-(Cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol

In the title compound, C(20)H(22)N(2)O(2), the asymmetric unit contains two independent half-mol­ecules, which are both completed by crystallographic inversion symmetry. The cyclo­hexane rings of both mol­ecules adopt chair conformations; the N atoms are in equatorial orientations in one mol­ecule a...

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Autores principales: Mohamed, Shaaban K., Akkurt, Mehmet, Tahir, Muhammad N., Abdelhamid, Antar A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379462/
https://www.ncbi.nlm.nih.gov/pubmed/22719660
http://dx.doi.org/10.1107/S1600536812023367
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author Mohamed, Shaaban K.
Akkurt, Mehmet
Tahir, Muhammad N.
Abdelhamid, Antar A.
author_facet Mohamed, Shaaban K.
Akkurt, Mehmet
Tahir, Muhammad N.
Abdelhamid, Antar A.
author_sort Mohamed, Shaaban K.
collection PubMed
description In the title compound, C(20)H(22)N(2)O(2), the asymmetric unit contains two independent half-mol­ecules, which are both completed by crystallographic inversion symmetry. The cyclo­hexane rings of both mol­ecules adopt chair conformations; the N atoms are in equatorial orientations in one mol­ecule and in axial orientations in the other. Both mol­ecules feature two intra­molecular O—H⋯N hydrogen bonds, which generate S(6) rings.
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spelling pubmed-33794622012-06-20 2,2′-[(E,E)-cis-(Cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol Mohamed, Shaaban K. Akkurt, Mehmet Tahir, Muhammad N. Abdelhamid, Antar A. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(22)N(2)O(2), the asymmetric unit contains two independent half-mol­ecules, which are both completed by crystallographic inversion symmetry. The cyclo­hexane rings of both mol­ecules adopt chair conformations; the N atoms are in equatorial orientations in one mol­ecule and in axial orientations in the other. Both mol­ecules feature two intra­molecular O—H⋯N hydrogen bonds, which generate S(6) rings. International Union of Crystallography 2012-05-26 /pmc/articles/PMC3379462/ /pubmed/22719660 http://dx.doi.org/10.1107/S1600536812023367 Text en © Mohamed 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
Mohamed, Shaaban K.
Akkurt, Mehmet
Tahir, Muhammad N.
Abdelhamid, Antar A.
2,2′-[(E,E)-cis-(Cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol
title 2,2′-[(E,E)-cis-(Cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol
title_full 2,2′-[(E,E)-cis-(Cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol
title_fullStr 2,2′-[(E,E)-cis-(Cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol
title_full_unstemmed 2,2′-[(E,E)-cis-(Cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol
title_short 2,2′-[(E,E)-cis-(Cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol
title_sort 2,2′-[(e,e)-cis-(cyclo­hexane-1,4-di­yl)bis­(nitrilo­methanylyl­idene)]diphenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379462/
https://www.ncbi.nlm.nih.gov/pubmed/22719660
http://dx.doi.org/10.1107/S1600536812023367
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