N,N′-Bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine

The title Schiff base compound, C(22)H(28)N(2)O(4), lies across a crystallographic inversion centre and adopts an E configuration with respect to the C=N bond. Pairs of weak inter­molecular C—H⋯O inter­actions link neighbouring mol­ecules into dimers with an R (2) (2)(28) ring motif. The crystal str...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Kia, Reza, Kargar, Hadi, Jamshidvand, Arezoo
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968861/
https://www.ncbi.nlm.nih.gov/pubmed/21582444
http://dx.doi.org/10.1107/S1600536809007545
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author Fun, Hoong-Kun
Kia, Reza
Kargar, Hadi
Jamshidvand, Arezoo
author_facet Fun, Hoong-Kun
Kia, Reza
Kargar, Hadi
Jamshidvand, Arezoo
author_sort Fun, Hoong-Kun
collection PubMed
description The title Schiff base compound, C(22)H(28)N(2)O(4), lies across a crystallographic inversion centre and adopts an E configuration with respect to the C=N bond. Pairs of weak inter­molecular C—H⋯O inter­actions link neighbouring mol­ecules into dimers with an R (2) (2)(28) ring motif. The crystal structure is stabilized by inter­molecular C—H⋯π inter­actions. An intramolecular O—H⋯N hydrogen bond occurs.
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spelling pubmed-29688612010-12-30 N,N′-Bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine Fun, Hoong-Kun Kia, Reza Kargar, Hadi Jamshidvand, Arezoo Acta Crystallogr Sect E Struct Rep Online Organic Papers The title Schiff base compound, C(22)H(28)N(2)O(4), lies across a crystallographic inversion centre and adopts an E configuration with respect to the C=N bond. Pairs of weak inter­molecular C—H⋯O inter­actions link neighbouring mol­ecules into dimers with an R (2) (2)(28) ring motif. The crystal structure is stabilized by inter­molecular C—H⋯π inter­actions. An intramolecular O—H⋯N hydrogen bond occurs. International Union of Crystallography 2009-03-06 /pmc/articles/PMC2968861/ /pubmed/21582444 http://dx.doi.org/10.1107/S1600536809007545 Text en © Fun 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
Fun, Hoong-Kun
Kia, Reza
Kargar, Hadi
Jamshidvand, Arezoo
N,N′-Bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine
title N,N′-Bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine
title_full N,N′-Bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine
title_fullStr N,N′-Bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine
title_full_unstemmed N,N′-Bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine
title_short N,N′-Bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine
title_sort n,n′-bis(2-hydr­oxy-3-eth­oxybenzyl­idene)butane-1,4-diamine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968861/
https://www.ncbi.nlm.nih.gov/pubmed/21582444
http://dx.doi.org/10.1107/S1600536809007545
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AT jamshidvandarezoo nnbis2hydroxy3ethoxybenzylidenebutane14diamine

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