Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1782236205464682496 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3379462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mohamedshaabank 22eeciscyclohexane14diylbisnitrilomethanylylidenediphenol AT akkurtmehmet 22eeciscyclohexane14diylbisnitrilomethanylylidenediphenol AT tahirmuhammadn 22eeciscyclohexane14diylbisnitrilomethanylylidenediphenol AT abdelhamidantara 22eeciscyclohexane14diylbisnitrilomethanylylidenediphenol |