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A monoclinic polymorph of (R,R)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol
The title compound, C(20)H(20)Br(2)N(2)O(2), a tetradentate Schiff base, is the enantiomerically pure R,R-diastereomer of four possible stereoisomers. The molecular structure reveals two strong intramolecular O—H⋯N hydrogen bonds between the hydroxy O atom and the imino N atom, which each gener...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344566/ https://www.ncbi.nlm.nih.gov/pubmed/22590328 http://dx.doi.org/10.1107/S1600536812016376 |
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author | Ha, Kwang |
author_facet | Ha, Kwang |
author_sort | Ha, Kwang |
collection | PubMed |
description | The title compound, C(20)H(20)Br(2)N(2)O(2), a tetradentate Schiff base, is the enantiomerically pure R,R-diastereomer of four possible stereoisomers. The molecular structure reveals two strong intramolecular O—H⋯N hydrogen bonds between the hydroxy O atom and the imino N atom, which each generate S(6) rings. In the crystal, molecules are stacked in columns along the a axis; when viewed down the b axis, successive columns are stacked in the opposite direction. The structure reported herein is the monoclinic polymorph of the previously reported orthorhombic form [Yi & Hu (2009 ▶). Acta Cryst. E65, o2643], in which the complete molecule is generated by a crystallographic twofold axis. |
format | Online Article Text |
id | pubmed-3344566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33445662012-05-15 A monoclinic polymorph of (R,R)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol Ha, Kwang Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(20)Br(2)N(2)O(2), a tetradentate Schiff base, is the enantiomerically pure R,R-diastereomer of four possible stereoisomers. The molecular structure reveals two strong intramolecular O—H⋯N hydrogen bonds between the hydroxy O atom and the imino N atom, which each generate S(6) rings. In the crystal, molecules are stacked in columns along the a axis; when viewed down the b axis, successive columns are stacked in the opposite direction. The structure reported herein is the monoclinic polymorph of the previously reported orthorhombic form [Yi & Hu (2009 ▶). Acta Cryst. E65, o2643], in which the complete molecule is generated by a crystallographic twofold axis. International Union of Crystallography 2012-04-21 /pmc/articles/PMC3344566/ /pubmed/22590328 http://dx.doi.org/10.1107/S1600536812016376 Text en © Kwang Ha 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 Ha, Kwang A monoclinic polymorph of (R,R)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol |
title | A monoclinic polymorph of (R,R)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol |
title_full | A monoclinic polymorph of (R,R)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol |
title_fullStr | A monoclinic polymorph of (R,R)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol |
title_full_unstemmed | A monoclinic polymorph of (R,R)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol |
title_short | A monoclinic polymorph of (R,R)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol |
title_sort | monoclinic polymorph of (r,r)-4,4′-dibromo-2,2′-[cyclohexane-1,2-diylbis(nitrilomethanylylidene)]diphenol |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344566/ https://www.ncbi.nlm.nih.gov/pubmed/22590328 http://dx.doi.org/10.1107/S1600536812016376 |
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