Cargando…
Quinoline-2-carbonitrile
In the title compound, C(10)H(6)N(2), the molecule is almost planar, with an r.m.s. deviation of 0.014 Å. The dihedral angle between the aromatic rings is 1.28 (16)°. In the crystal, molecules are stacked along the a axis by way of weak aromatic π–π stacking interactions between the benzene and p...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008022/ https://www.ncbi.nlm.nih.gov/pubmed/21588729 http://dx.doi.org/10.1107/S1600536810033118 |
_version_ | 1782194483499106304 |
---|---|
author | Loh, Wan-Sin Quah, Ching Kheng Hemamalini, Madhukar Fun, Hoong-Kun |
author_facet | Loh, Wan-Sin Quah, Ching Kheng Hemamalini, Madhukar Fun, Hoong-Kun |
author_sort | Loh, Wan-Sin |
collection | PubMed |
description | In the title compound, C(10)H(6)N(2), the molecule is almost planar, with an r.m.s. deviation of 0.014 Å. The dihedral angle between the aromatic rings is 1.28 (16)°. In the crystal, molecules are stacked along the a axis by way of weak aromatic π–π stacking interactions between the benzene and pyridine rings of adjacent molecules [centroid–centroid separation = 3.7943 (19) Å]. |
format | Text |
id | pubmed-3008022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30080222010-12-30 Quinoline-2-carbonitrile Loh, Wan-Sin Quah, Ching Kheng Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(6)N(2), the molecule is almost planar, with an r.m.s. deviation of 0.014 Å. The dihedral angle between the aromatic rings is 1.28 (16)°. In the crystal, molecules are stacked along the a axis by way of weak aromatic π–π stacking interactions between the benzene and pyridine rings of adjacent molecules [centroid–centroid separation = 3.7943 (19) Å]. International Union of Crystallography 2010-08-25 /pmc/articles/PMC3008022/ /pubmed/21588729 http://dx.doi.org/10.1107/S1600536810033118 Text en © Loh et al. 2010 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 Loh, Wan-Sin Quah, Ching Kheng Hemamalini, Madhukar Fun, Hoong-Kun Quinoline-2-carbonitrile |
title | Quinoline-2-carbonitrile |
title_full | Quinoline-2-carbonitrile |
title_fullStr | Quinoline-2-carbonitrile |
title_full_unstemmed | Quinoline-2-carbonitrile |
title_short | Quinoline-2-carbonitrile |
title_sort | quinoline-2-carbonitrile |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008022/ https://www.ncbi.nlm.nih.gov/pubmed/21588729 http://dx.doi.org/10.1107/S1600536810033118 |
work_keys_str_mv | AT lohwansin quinoline2carbonitrile AT quahchingkheng quinoline2carbonitrile AT hemamalinimadhukar quinoline2carbonitrile AT funhoongkun quinoline2carbonitrile |