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4,6,10,12,16,18,22,24-Octa-O-methyl-2,8,14,20-tetrapentylresorcin[4]arene
The complete molecule of the title compound, C(56)H(80)O(8), is generated by a crystallographic inversion centre. The dihedral angle between the aromatic ring and the unique half of the molecule is 81.52 (16)°. There are no π–π interactions in the crystal structure.
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2011
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201257/ https://www.ncbi.nlm.nih.gov/pubmed/22058735 http://dx.doi.org/10.1107/S1600536811034003 |
| _version_ | 1782214833235558400 |
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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 complete molecule of the title compound, C(56)H(80)O(8), is generated by a crystallographic inversion centre. The dihedral angle between the aromatic ring and the unique half of the molecule is 81.52 (16)°. There are no π–π interactions in the crystal structure. |
| format | Online Article Text |
| id | pubmed-3201257 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2011 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-32012572011-11-06 4,6,10,12,16,18,22,24-Octa-O-methyl-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 complete molecule of the title compound, C(56)H(80)O(8), is generated by a crystallographic inversion centre. The dihedral angle between the aromatic ring and the unique half of the molecule is 81.52 (16)°. There are no π–π interactions in the crystal structure. International Union of Crystallography 2011-09-14 /pmc/articles/PMC3201257/ /pubmed/22058735 http://dx.doi.org/10.1107/S1600536811034003 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. 4,6,10,12,16,18,22,24-Octa-O-methyl-2,8,14,20-tetrapentylresorcin[4]arene |
| title | 4,6,10,12,16,18,22,24-Octa-O-methyl-2,8,14,20-tetrapentylresorcin[4]arene |
| title_full | 4,6,10,12,16,18,22,24-Octa-O-methyl-2,8,14,20-tetrapentylresorcin[4]arene |
| title_fullStr | 4,6,10,12,16,18,22,24-Octa-O-methyl-2,8,14,20-tetrapentylresorcin[4]arene |
| title_full_unstemmed | 4,6,10,12,16,18,22,24-Octa-O-methyl-2,8,14,20-tetrapentylresorcin[4]arene |
| title_short | 4,6,10,12,16,18,22,24-Octa-O-methyl-2,8,14,20-tetrapentylresorcin[4]arene |
| title_sort | 4,6,10,12,16,18,22,24-octa-o-methyl-2,8,14,20-tetrapentylresorcin[4]arene |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201257/ https://www.ncbi.nlm.nih.gov/pubmed/22058735 http://dx.doi.org/10.1107/S1600536811034003 |
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