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4,5,6,10,11,12,16,17,18,22,23,24-Dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene

The title compound, C(84)H(112)O(36), has a macrocyclic structure. It has 12 (meth­oxy­carbon­yl)meth­oxy ‘head groups’ in the upper rim and exhibits a flattened boat geometry. Intra­molecular C—H⋯O hydrogen bonds occur. In the crystal, inter­molecular C—H⋯O contacts occur. The ‘head groups’ and the...

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Detalles Bibliográficos
Autores principales: Pansuriya, Pramod B., Friedrich, Holger B., Maguire, Glenn E. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238958/
https://www.ncbi.nlm.nih.gov/pubmed/22199807
http://dx.doi.org/10.1107/S1600536811047180
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author Pansuriya, Pramod B.
Friedrich, Holger B.
Maguire, Glenn E. M.
author_facet Pansuriya, Pramod B.
Friedrich, Holger B.
Maguire, Glenn E. M.
author_sort Pansuriya, Pramod B.
collection PubMed
description The title compound, C(84)H(112)O(36), has a macrocyclic structure. It has 12 (meth­oxy­carbon­yl)meth­oxy ‘head groups’ in the upper rim and exhibits a flattened boat geometry. Intra­molecular C—H⋯O hydrogen bonds occur. In the crystal, inter­molecular C—H⋯O contacts occur. The ‘head groups’ and the pentyl ‘feet’ contain disordered (0.5:0.5 occupancy ratio) atoms.
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spelling pubmed-32389582011-12-23 4,5,6,10,11,12,16,17,18,22,23,24-Dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene Pansuriya, Pramod B. Friedrich, Holger B. Maguire, Glenn E. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(84)H(112)O(36), has a macrocyclic structure. It has 12 (meth­oxy­carbon­yl)meth­oxy ‘head groups’ in the upper rim and exhibits a flattened boat geometry. Intra­molecular C—H⋯O hydrogen bonds occur. In the crystal, inter­molecular C—H⋯O contacts occur. The ‘head groups’ and the pentyl ‘feet’ contain disordered (0.5:0.5 occupancy ratio) atoms. International Union of Crystallography 2011-11-16 /pmc/articles/PMC3238958/ /pubmed/22199807 http://dx.doi.org/10.1107/S1600536811047180 Text en © Pansuriya et al. 2011 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
Pansuriya, Pramod B.
Friedrich, Holger B.
Maguire, Glenn E. M.
4,5,6,10,11,12,16,17,18,22,23,24-Dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene
title 4,5,6,10,11,12,16,17,18,22,23,24-Dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene
title_full 4,5,6,10,11,12,16,17,18,22,23,24-Dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene
title_fullStr 4,5,6,10,11,12,16,17,18,22,23,24-Dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene
title_full_unstemmed 4,5,6,10,11,12,16,17,18,22,23,24-Dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene
title_short 4,5,6,10,11,12,16,17,18,22,23,24-Dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene
title_sort 4,5,6,10,11,12,16,17,18,22,23,24-dodeca­kis­[(meth­oxy­carbon­yl)meth­oxy]-2,8,14,20-tetra­pentyl­resorcin[4]arene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238958/
https://www.ncbi.nlm.nih.gov/pubmed/22199807
http://dx.doi.org/10.1107/S1600536811047180
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