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N-Cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide
The molecule of the title compound, C(24)H(36)N(2)O(2)S, displays a U-shaped conformation. The prominent intermolecular interactions are N—H⋯O hydrogen bonds, resulting in the formation of dimers. Additional C—H⋯π contacts involving one of the methylene groups of the macrocycle and the naphthalen...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961696/ https://www.ncbi.nlm.nih.gov/pubmed/21202844 http://dx.doi.org/10.1107/S1600536808016164 |
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author | Fischer, Conrad Gruber, Tobias Seichter, Wilhelm Weber, Edwin Ibragimov, Bakhtiyar T. |
author_facet | Fischer, Conrad Gruber, Tobias Seichter, Wilhelm Weber, Edwin Ibragimov, Bakhtiyar T. |
author_sort | Fischer, Conrad |
collection | PubMed |
description | The molecule of the title compound, C(24)H(36)N(2)O(2)S, displays a U-shaped conformation. The prominent intermolecular interactions are N—H⋯O hydrogen bonds, resulting in the formation of dimers. Additional C—H⋯π contacts involving one of the methylene groups of the macrocycle and the naphthalene rings of a neighbouring molecule stabilize the packing structure. In the crystal structure, the cyclododecyl ring is disordered over two positions; the site occupancy factors are ca 0.86 and 0.14. |
format | Text |
id | pubmed-2961696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29616962010-12-30 N-Cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide Fischer, Conrad Gruber, Tobias Seichter, Wilhelm Weber, Edwin Ibragimov, Bakhtiyar T. Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecule of the title compound, C(24)H(36)N(2)O(2)S, displays a U-shaped conformation. The prominent intermolecular interactions are N—H⋯O hydrogen bonds, resulting in the formation of dimers. Additional C—H⋯π contacts involving one of the methylene groups of the macrocycle and the naphthalene rings of a neighbouring molecule stabilize the packing structure. In the crystal structure, the cyclododecyl ring is disordered over two positions; the site occupancy factors are ca 0.86 and 0.14. International Union of Crystallography 2008-06-07 /pmc/articles/PMC2961696/ /pubmed/21202844 http://dx.doi.org/10.1107/S1600536808016164 Text en © Fischer 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 Fischer, Conrad Gruber, Tobias Seichter, Wilhelm Weber, Edwin Ibragimov, Bakhtiyar T. N-Cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide |
title |
N-Cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide |
title_full |
N-Cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide |
title_fullStr |
N-Cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide |
title_full_unstemmed |
N-Cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide |
title_short |
N-Cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide |
title_sort | n-cyclododecyl-5-(dimethylamino)naphthalene-1-sulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961696/ https://www.ncbi.nlm.nih.gov/pubmed/21202844 http://dx.doi.org/10.1107/S1600536808016164 |
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