Bis(2-hydroxy­benzaldehyde oxime) O,O′-butane-1,4-diyldicarbonyl ether

The mol­ecule of the title compound, C(20)H(20)N(2)O(6), lies across a crystallographic inversion centre, the asymmetric unit comprising one half-mol­ecule. An intra­molecular O—H⋯N hydrogen bond generates a six-membered ring, producing an S(6) ring motif. Pairs of inter­molecular C—H⋯O hydrogen bon...

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Detalles Bibliográficos
Autores principales: Etemadi, Bijan, Kia, Reza, Sharghi, Hashem, Hosseini Sarvari, Mona
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969837/
https://www.ncbi.nlm.nih.gov/pubmed/21583166
http://dx.doi.org/10.1107/S1600536809016663
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author Etemadi, Bijan
Kia, Reza
Sharghi, Hashem
Hosseini Sarvari, Mona
author_facet Etemadi, Bijan
Kia, Reza
Sharghi, Hashem
Hosseini Sarvari, Mona
author_sort Etemadi, Bijan
collection PubMed
description The mol­ecule of the title compound, C(20)H(20)N(2)O(6), lies across a crystallographic inversion centre, the asymmetric unit comprising one half-mol­ecule. An intra­molecular O—H⋯N hydrogen bond generates a six-membered ring, producing an S(6) ring motif. Pairs of inter­molecular C—H⋯O hydrogen bonds link neighbouring mol­ecules into a layer with R (2) (2)(38) ring motif. The crystal structure is further stabilized by the inter­molecular C—H⋯π inter­actions.
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spelling pubmed-29698372010-12-30 Bis(2-hydroxy­benzaldehyde oxime) O,O′-butane-1,4-diyldicarbonyl ether Etemadi, Bijan Kia, Reza Sharghi, Hashem Hosseini Sarvari, Mona Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(20)H(20)N(2)O(6), lies across a crystallographic inversion centre, the asymmetric unit comprising one half-mol­ecule. An intra­molecular O—H⋯N hydrogen bond generates a six-membered ring, producing an S(6) ring motif. Pairs of inter­molecular C—H⋯O hydrogen bonds link neighbouring mol­ecules into a layer with R (2) (2)(38) ring motif. The crystal structure is further stabilized by the inter­molecular C—H⋯π inter­actions. International Union of Crystallography 2009-05-20 /pmc/articles/PMC2969837/ /pubmed/21583166 http://dx.doi.org/10.1107/S1600536809016663 Text en © Etemadi et al. 2009 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
Etemadi, Bijan
Kia, Reza
Sharghi, Hashem
Hosseini Sarvari, Mona
Bis(2-hydroxy­benzaldehyde oxime) O,O′-butane-1,4-diyldicarbonyl ether
title Bis(2-hydroxy­benzaldehyde oxime) O,O′-butane-1,4-diyldicarbonyl ether
title_full Bis(2-hydroxy­benzaldehyde oxime) O,O′-butane-1,4-diyldicarbonyl ether
title_fullStr Bis(2-hydroxy­benzaldehyde oxime) O,O′-butane-1,4-diyldicarbonyl ether
title_full_unstemmed Bis(2-hydroxy­benzaldehyde oxime) O,O′-butane-1,4-diyldicarbonyl ether
title_short Bis(2-hydroxy­benzaldehyde oxime) O,O′-butane-1,4-diyldicarbonyl ether
title_sort bis(2-hydroxy­benzaldehyde oxime) o,o′-butane-1,4-diyldicarbonyl ether
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969837/
https://www.ncbi.nlm.nih.gov/pubmed/21583166
http://dx.doi.org/10.1107/S1600536809016663
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AT kiareza bis2hydroxybenzaldehydeoximeoobutane14diyldicarbonylether
AT sharghihashem bis2hydroxybenzaldehydeoximeoobutane14diyldicarbonylether
AT hosseinisarvarimona bis2hydroxybenzaldehydeoximeoobutane14diyldicarbonylether

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