2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol

The title compound, C(28)H(28)N(2)O(4), was synthesized by the reaction of 2-acetyl-1-naphthol with 1,4-bis­(amino­oxy)butane in ethanol. The molecule, which lies about an inversion centre, adopts a linear structure, in which the oxime groups and naphthalene ring systems assume an anti conformation....

Descripción completa

Detalles Bibliográficos
Autores principales: Dong, Wen-Kui, Wu, Jian-Chao, Sun, Yin-Xia, Yao, Jian, Tong, Jun-Feng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969537/
https://www.ncbi.nlm.nih.gov/pubmed/21583113
http://dx.doi.org/10.1107/S160053680901647X
_version_ 1782190181506351104
author Dong, Wen-Kui
Wu, Jian-Chao
Sun, Yin-Xia
Yao, Jian
Tong, Jun-Feng
author_facet Dong, Wen-Kui
Wu, Jian-Chao
Sun, Yin-Xia
Yao, Jian
Tong, Jun-Feng
author_sort Dong, Wen-Kui
collection PubMed
description The title compound, C(28)H(28)N(2)O(4), was synthesized by the reaction of 2-acetyl-1-naphthol with 1,4-bis­(amino­oxy)butane in ethanol. The molecule, which lies about an inversion centre, adopts a linear structure, in which the oxime groups and naphthalene ring systems assume an anti conformation. The intra­molecular inter­planar distance between parallel naphthalene rings is 1.054 (3) Å. Intra­molecular O—H⋯N hydrogen bonds are formed between the oxime nitro­gen and hydr­oxy groups.
format Text
id pubmed-2969537
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29695372010-12-30 2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol Dong, Wen-Kui Wu, Jian-Chao Sun, Yin-Xia Yao, Jian Tong, Jun-Feng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(28)H(28)N(2)O(4), was synthesized by the reaction of 2-acetyl-1-naphthol with 1,4-bis­(amino­oxy)butane in ethanol. The molecule, which lies about an inversion centre, adopts a linear structure, in which the oxime groups and naphthalene ring systems assume an anti conformation. The intra­molecular inter­planar distance between parallel naphthalene rings is 1.054 (3) Å. Intra­molecular O—H⋯N hydrogen bonds are formed between the oxime nitro­gen and hydr­oxy groups. International Union of Crystallography 2009-05-14 /pmc/articles/PMC2969537/ /pubmed/21583113 http://dx.doi.org/10.1107/S160053680901647X Text en © Dong 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
Dong, Wen-Kui
Wu, Jian-Chao
Sun, Yin-Xia
Yao, Jian
Tong, Jun-Feng
2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol
title 2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol
title_full 2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol
title_fullStr 2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol
title_full_unstemmed 2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol
title_short 2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol
title_sort 2,2′-{1,1′-[butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969537/
https://www.ncbi.nlm.nih.gov/pubmed/21583113
http://dx.doi.org/10.1107/S160053680901647X
work_keys_str_mv AT dongwenkui 2211butane14diylbisoxynitrilodiethylidynedi1naphthol
AT wujianchao 2211butane14diylbisoxynitrilodiethylidynedi1naphthol
AT sunyinxia 2211butane14diylbisoxynitrilodiethylidynedi1naphthol
AT yaojian 2211butane14diylbisoxynitrilodiethylidynedi1naphthol
AT tongjunfeng 2211butane14diylbisoxynitrilodiethylidynedi1naphthol

Ejemplares similares