5-Phenyl-2-(4-pyrid­yl)pyrimidine

The title compound, C(15)H(11)N(3), crystallizes with two independent mol­ecules in the asymmetric unit. The dihedral angles between the phenyl and pyridine rings in each mol­ecule are 53.48 (5) and 50.80 (5)°. In the crystal structure, weak inter­molecular C—H⋯N hydrogen bonds connect mol­ecules in...

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Detalles Bibliográficos
Autores principales: Santoni, Marie-Pierre C., Yu, Siu Hong, Hanan, Garry S., Proust, Anna, Hasenknopf, Bernold
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960877/
https://www.ncbi.nlm.nih.gov/pubmed/21201923
http://dx.doi.org/10.1107/S160053680800398X
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author Santoni, Marie-Pierre C.
Yu, Siu Hong
Hanan, Garry S.
Proust, Anna
Hasenknopf, Bernold
author_facet Santoni, Marie-Pierre C.
Yu, Siu Hong
Hanan, Garry S.
Proust, Anna
Hasenknopf, Bernold
author_sort Santoni, Marie-Pierre C.
collection PubMed
description The title compound, C(15)H(11)N(3), crystallizes with two independent mol­ecules in the asymmetric unit. The dihedral angles between the phenyl and pyridine rings in each mol­ecule are 53.48 (5) and 50.80 (5)°. In the crystal structure, weak inter­molecular C—H⋯N hydrogen bonds connect mol­ecules into one-dimensional chains. In addition, the crystal structure is stabilized by weak C—H⋯π(arene) inter­actions.
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spelling pubmed-29608772010-12-30 5-Phenyl-2-(4-pyrid­yl)pyrimidine Santoni, Marie-Pierre C. Yu, Siu Hong Hanan, Garry S. Proust, Anna Hasenknopf, Bernold Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(11)N(3), crystallizes with two independent mol­ecules in the asymmetric unit. The dihedral angles between the phenyl and pyridine rings in each mol­ecule are 53.48 (5) and 50.80 (5)°. In the crystal structure, weak inter­molecular C—H⋯N hydrogen bonds connect mol­ecules into one-dimensional chains. In addition, the crystal structure is stabilized by weak C—H⋯π(arene) inter­actions. International Union of Crystallography 2008-02-13 /pmc/articles/PMC2960877/ /pubmed/21201923 http://dx.doi.org/10.1107/S160053680800398X Text en © Santoni 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
Santoni, Marie-Pierre C.
Yu, Siu Hong
Hanan, Garry S.
Proust, Anna
Hasenknopf, Bernold
5-Phenyl-2-(4-pyrid­yl)pyrimidine
title 5-Phenyl-2-(4-pyrid­yl)pyrimidine
title_full 5-Phenyl-2-(4-pyrid­yl)pyrimidine
title_fullStr 5-Phenyl-2-(4-pyrid­yl)pyrimidine
title_full_unstemmed 5-Phenyl-2-(4-pyrid­yl)pyrimidine
title_short 5-Phenyl-2-(4-pyrid­yl)pyrimidine
title_sort 5-phenyl-2-(4-pyrid­yl)pyrimidine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960877/
https://www.ncbi.nlm.nih.gov/pubmed/21201923
http://dx.doi.org/10.1107/S160053680800398X
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AT yusiuhong 5phenyl24pyridylpyrimidine
AT hanangarrys 5phenyl24pyridylpyrimidine
AT proustanna 5phenyl24pyridylpyrimidine
AT hasenknopfbernold 5phenyl24pyridylpyrimidine

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