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Partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene
Molecules of the title compound, C(40)H(44)O(8), adopt a partial cone conformation. The dihedral angles between the planes of the aromatic rings and the mean plane through the methylene C atoms bridging the aromatic rings are 35.74 (7), 85.86 (5), 87.77 (4) and 89.95 (5)°. Two opposite aryl rings...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960911/ https://www.ncbi.nlm.nih.gov/pubmed/21202103 http://dx.doi.org/10.1107/S1600536808006843 |
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author | Zhang, Guo-Zhi Zhao, Mei Zhang, Xiao-Ling Ma, Jian-Ping Guo, Dian-Shun |
author_facet | Zhang, Guo-Zhi Zhao, Mei Zhang, Xiao-Ling Ma, Jian-Ping Guo, Dian-Shun |
author_sort | Zhang, Guo-Zhi |
collection | PubMed |
description | Molecules of the title compound, C(40)H(44)O(8), adopt a partial cone conformation. The dihedral angles between the planes of the aromatic rings and the mean plane through the methylene C atoms bridging the aromatic rings are 35.74 (7), 85.86 (5), 87.77 (4) and 89.95 (5)°. Two opposite aryl rings are approximately parallel to each other; the others are at an interplanar angle of 52.41 (6)°. Intra- and intermolecular C—H⋯O hydrogen bonds stabilize the molecular conformation and the crystal packing. Two C atoms of one propoxy chain are disordered over two positions; the site occupancy factors are ca 0.66 and 0.34. |
format | Text |
id | pubmed-2960911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29609112010-12-30 Partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene Zhang, Guo-Zhi Zhao, Mei Zhang, Xiao-Ling Ma, Jian-Ping Guo, Dian-Shun Acta Crystallogr Sect E Struct Rep Online Organic Papers Molecules of the title compound, C(40)H(44)O(8), adopt a partial cone conformation. The dihedral angles between the planes of the aromatic rings and the mean plane through the methylene C atoms bridging the aromatic rings are 35.74 (7), 85.86 (5), 87.77 (4) and 89.95 (5)°. Two opposite aryl rings are approximately parallel to each other; the others are at an interplanar angle of 52.41 (6)°. Intra- and intermolecular C—H⋯O hydrogen bonds stabilize the molecular conformation and the crystal packing. Two C atoms of one propoxy chain are disordered over two positions; the site occupancy factors are ca 0.66 and 0.34. International Union of Crystallography 2008-03-14 /pmc/articles/PMC2960911/ /pubmed/21202103 http://dx.doi.org/10.1107/S1600536808006843 Text en © Zhang et al. 2008 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, Guo-Zhi Zhao, Mei Zhang, Xiao-Ling Ma, Jian-Ping Guo, Dian-Shun Partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene |
title | Partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene |
title_full | Partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene |
title_fullStr | Partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene |
title_full_unstemmed | Partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene |
title_short | Partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene |
title_sort | partial cone conformer of 25,27-bis[(methoxycarbonyl)methoxy]-26,28-dipropoxycalix[4]arene |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960911/ https://www.ncbi.nlm.nih.gov/pubmed/21202103 http://dx.doi.org/10.1107/S1600536808006843 |
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