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4-(Naphthalen-1-yl)pyridine
In the title compound, C(15)H(11)N, the mean planes of the aromatic moieties are inclined to one another by 72.9 (1)°. The crystal is stabilized by π–π stacking interactions between the pyridine rings of inversion-related molecules, with a centroid–centroid distance of 3.772 (2) Å. In addition, C—...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952235/ https://www.ncbi.nlm.nih.gov/pubmed/24627683 http://dx.doi.org/10.1107/S1600536813014372 |
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author | Vetter, Antje Seichter, Wilhelm Weber, Edwin |
author_facet | Vetter, Antje Seichter, Wilhelm Weber, Edwin |
author_sort | Vetter, Antje |
collection | PubMed |
description | In the title compound, C(15)H(11)N, the mean planes of the aromatic moieties are inclined to one another by 72.9 (1)°. The crystal is stabilized by π–π stacking interactions between the pyridine rings of inversion-related molecules, with a centroid–centroid distance of 3.772 (2) Å. In addition, C—H⋯π contacts involving an α-C—H group of the pyridine ring and the nonsubstituted ring of the naphthalene unit are observed, giving rise to a herringbone-type supramolecular architecture of the naphthalene moiety being contained in the molecule. |
format | Online Article Text |
id | pubmed-3952235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-39522352014-03-13 4-(Naphthalen-1-yl)pyridine Vetter, Antje Seichter, Wilhelm Weber, Edwin Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(11)N, the mean planes of the aromatic moieties are inclined to one another by 72.9 (1)°. The crystal is stabilized by π–π stacking interactions between the pyridine rings of inversion-related molecules, with a centroid–centroid distance of 3.772 (2) Å. In addition, C—H⋯π contacts involving an α-C—H group of the pyridine ring and the nonsubstituted ring of the naphthalene unit are observed, giving rise to a herringbone-type supramolecular architecture of the naphthalene moiety being contained in the molecule. International Union of Crystallography 2013-06-08 /pmc/articles/PMC3952235/ /pubmed/24627683 http://dx.doi.org/10.1107/S1600536813014372 Text en © Vetter et al. 2013 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 Vetter, Antje Seichter, Wilhelm Weber, Edwin 4-(Naphthalen-1-yl)pyridine |
title | 4-(Naphthalen-1-yl)pyridine |
title_full | 4-(Naphthalen-1-yl)pyridine |
title_fullStr | 4-(Naphthalen-1-yl)pyridine |
title_full_unstemmed | 4-(Naphthalen-1-yl)pyridine |
title_short | 4-(Naphthalen-1-yl)pyridine |
title_sort | 4-(naphthalen-1-yl)pyridine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952235/ https://www.ncbi.nlm.nih.gov/pubmed/24627683 http://dx.doi.org/10.1107/S1600536813014372 |
work_keys_str_mv | AT vetterantje 4naphthalen1ylpyridine AT seichterwilhelm 4naphthalen1ylpyridine AT weberedwin 4naphthalen1ylpyridine |