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...

Descripción completa

Detalles Bibliográficos
Autores principales: Loh, Wan-Sin, Quah, Ching Kheng, Hemamalini, Madhukar, Fun, Hoong-Kun
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