3,9-Di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne

In the title compound, C(27)H(24)O(4), the 1,3-dioxane rings have chair conformations. The mol­ecule has non-crystallographic twofold rotation symmetry. The dihedral angle between the naphthalene ring systems is 17.96(4)° In the crystal structure, weak inter­molecular C—H⋯π inter­actions contribute...

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Detalles Bibliográficos
Autores principales: Zhang, Xiuqin, Cui, Yuan, Yu, Bin, Sun, Xiaoqiang, Chen, Qiang
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979257/
https://www.ncbi.nlm.nih.gov/pubmed/21579228
http://dx.doi.org/10.1107/S1600536810014741
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author Zhang, Xiuqin
Cui, Yuan
Yu, Bin
Sun, Xiaoqiang
Chen, Qiang
author_facet Zhang, Xiuqin
Cui, Yuan
Yu, Bin
Sun, Xiaoqiang
Chen, Qiang
author_sort Zhang, Xiuqin
collection PubMed
description In the title compound, C(27)H(24)O(4), the 1,3-dioxane rings have chair conformations. The mol­ecule has non-crystallographic twofold rotation symmetry. The dihedral angle between the naphthalene ring systems is 17.96(4)° In the crystal structure, weak inter­molecular C—H⋯π inter­actions contribute to the crystal packing.
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spelling pubmed-29792572010-12-30 3,9-Di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne Zhang, Xiuqin Cui, Yuan Yu, Bin Sun, Xiaoqiang Chen, Qiang Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(27)H(24)O(4), the 1,3-dioxane rings have chair conformations. The mol­ecule has non-crystallographic twofold rotation symmetry. The dihedral angle between the naphthalene ring systems is 17.96(4)° In the crystal structure, weak inter­molecular C—H⋯π inter­actions contribute to the crystal packing. International Union of Crystallography 2010-04-28 /pmc/articles/PMC2979257/ /pubmed/21579228 http://dx.doi.org/10.1107/S1600536810014741 Text en © Zhang et al. 2010 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
Zhang, Xiuqin
Cui, Yuan
Yu, Bin
Sun, Xiaoqiang
Chen, Qiang
3,9-Di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne
title 3,9-Di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne
title_full 3,9-Di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne
title_fullStr 3,9-Di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne
title_full_unstemmed 3,9-Di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne
title_short 3,9-Di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne
title_sort 3,9-di-1-naphthyl-2,4,8,10-tetra­oxa­spiro­[5.5]undeca­ne
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979257/
https://www.ncbi.nlm.nih.gov/pubmed/21579228
http://dx.doi.org/10.1107/S1600536810014741
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