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5,17-Diformyl-25,26,27,28-tetrapropoxycalix[4]arene
The title compound, C(42)H(48)O(6), was obtained via formylation of 25,26,27,28-tetrapropoxycalix[4]arene with dichloromethyl methyl ether and tin tetrachloride. It adopts a pinched cone conformation, which leads to an open cavity. The two opposite aromatic rings bearing formyl groups are almost...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588550/ https://www.ncbi.nlm.nih.gov/pubmed/23476597 http://dx.doi.org/10.1107/S1600536813004625 |
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author | Li, Zhengyi Ma, Hongzhao Lai, Yuan Chen, Liang Sun, Xiaoqiang |
author_facet | Li, Zhengyi Ma, Hongzhao Lai, Yuan Chen, Liang Sun, Xiaoqiang |
author_sort | Li, Zhengyi |
collection | PubMed |
description | The title compound, C(42)H(48)O(6), was obtained via formylation of 25,26,27,28-tetrapropoxycalix[4]arene with dichloromethyl methyl ether and tin tetrachloride. It adopts a pinched cone conformation, which leads to an open cavity. The two opposite aromatic rings bearing formyl groups are almost parallel, making a dihedral angle of 29.1 (2)°. The other pair of opposite rings are close to being perpendicular, making a dihedral angle of 73.6 (1)°. Adjacent rings are almost perpendicular, making dihedral angles of 78.8 (2), 81.6 (1), 78.2 (1) and 74.7 (1)°. |
format | Online Article Text |
id | pubmed-3588550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35885502013-03-08 5,17-Diformyl-25,26,27,28-tetrapropoxycalix[4]arene Li, Zhengyi Ma, Hongzhao Lai, Yuan Chen, Liang Sun, Xiaoqiang Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(42)H(48)O(6), was obtained via formylation of 25,26,27,28-tetrapropoxycalix[4]arene with dichloromethyl methyl ether and tin tetrachloride. It adopts a pinched cone conformation, which leads to an open cavity. The two opposite aromatic rings bearing formyl groups are almost parallel, making a dihedral angle of 29.1 (2)°. The other pair of opposite rings are close to being perpendicular, making a dihedral angle of 73.6 (1)°. Adjacent rings are almost perpendicular, making dihedral angles of 78.8 (2), 81.6 (1), 78.2 (1) and 74.7 (1)°. International Union of Crystallography 2013-02-23 /pmc/articles/PMC3588550/ /pubmed/23476597 http://dx.doi.org/10.1107/S1600536813004625 Text en © Li et al. 2013 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 Li, Zhengyi Ma, Hongzhao Lai, Yuan Chen, Liang Sun, Xiaoqiang 5,17-Diformyl-25,26,27,28-tetrapropoxycalix[4]arene |
title | 5,17-Diformyl-25,26,27,28-tetrapropoxycalix[4]arene |
title_full | 5,17-Diformyl-25,26,27,28-tetrapropoxycalix[4]arene |
title_fullStr | 5,17-Diformyl-25,26,27,28-tetrapropoxycalix[4]arene |
title_full_unstemmed | 5,17-Diformyl-25,26,27,28-tetrapropoxycalix[4]arene |
title_short | 5,17-Diformyl-25,26,27,28-tetrapropoxycalix[4]arene |
title_sort | 5,17-diformyl-25,26,27,28-tetrapropoxycalix[4]arene |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588550/ https://www.ncbi.nlm.nih.gov/pubmed/23476597 http://dx.doi.org/10.1107/S1600536813004625 |
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