4-[2-(4-Fluoro­phen­yl)furan-3-yl]pyridine

In the crystal structure of the title compound, C(15)H(10)FNO, the furan ring makes dihedral angles of 40.04 (11) and 25.71 (11)° with the pyridine and 4-fluoro­phenyl rings, respectively. The pyridine ring makes a dihedral angle of 49.51 (10)° with the 4-fluoro­phenyl ring. Non-conventional C—H⋯F a...

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Detalles Bibliográficos
Autores principales: Abu Thaher, Bassam, Koch, Pierre, Schollmeyer, Dieter, Laufer, Stefan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968695/
https://www.ncbi.nlm.nih.gov/pubmed/21582130
http://dx.doi.org/10.1107/S1600536809003651
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author Abu Thaher, Bassam
Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
author_facet Abu Thaher, Bassam
Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
author_sort Abu Thaher, Bassam
collection PubMed
description In the crystal structure of the title compound, C(15)H(10)FNO, the furan ring makes dihedral angles of 40.04 (11) and 25.71 (11)° with the pyridine and 4-fluoro­phenyl rings, respectively. The pyridine ring makes a dihedral angle of 49.51 (10)° with the 4-fluoro­phenyl ring. Non-conventional C—H⋯F and C—H⋯N hydrogen bonds are effective in the stabilization of the crystal structure.
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spelling pubmed-29686952010-12-30 4-[2-(4-Fluoro­phen­yl)furan-3-yl]pyridine Abu Thaher, Bassam Koch, Pierre Schollmeyer, Dieter Laufer, Stefan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(15)H(10)FNO, the furan ring makes dihedral angles of 40.04 (11) and 25.71 (11)° with the pyridine and 4-fluoro­phenyl rings, respectively. The pyridine ring makes a dihedral angle of 49.51 (10)° with the 4-fluoro­phenyl ring. Non-conventional C—H⋯F and C—H⋯N hydrogen bonds are effective in the stabilization of the crystal structure. International Union of Crystallography 2009-02-04 /pmc/articles/PMC2968695/ /pubmed/21582130 http://dx.doi.org/10.1107/S1600536809003651 Text en © Abu Thaher et al. 2009 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
Abu Thaher, Bassam
Koch, Pierre
Schollmeyer, Dieter
Laufer, Stefan
4-[2-(4-Fluoro­phen­yl)furan-3-yl]pyridine
title 4-[2-(4-Fluoro­phen­yl)furan-3-yl]pyridine
title_full 4-[2-(4-Fluoro­phen­yl)furan-3-yl]pyridine
title_fullStr 4-[2-(4-Fluoro­phen­yl)furan-3-yl]pyridine
title_full_unstemmed 4-[2-(4-Fluoro­phen­yl)furan-3-yl]pyridine
title_short 4-[2-(4-Fluoro­phen­yl)furan-3-yl]pyridine
title_sort 4-[2-(4-fluoro­phen­yl)furan-3-yl]pyridine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968695/
https://www.ncbi.nlm.nih.gov/pubmed/21582130
http://dx.doi.org/10.1107/S1600536809003651
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AT kochpierre 424fluorophenylfuran3ylpyridine
AT schollmeyerdieter 424fluorophenylfuran3ylpyridine
AT lauferstefan 424fluorophenylfuran3ylpyridine

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