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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...

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Autores principales: Zhang, Guo-Zhi, Zhao, Mei, Zhang, Xiao-Ling, Ma, Jian-Ping, Guo, Dian-Shun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
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.
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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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