2-Phenyl-4,5-di-2-pyridyl-1H-imidazole

In the title compound, C(19)H(14)N(4), which was crystallized from dimethyl sulfoxide, the arene and heterocyclic rings of the lophine analogue framework differ only slightly from coplanarity (dihedral angles range from 8.8 to 20.2°), and intramolecular N—H⋯N and C—H⋯N interactions help to establish...

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Detalles Bibliográficos
Autores principales: Felsmann, Marika, Schindler, Diana, Weber, Edwin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980126/
https://www.ncbi.nlm.nih.gov/pubmed/21580039
http://dx.doi.org/10.1107/S1600536809053215
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author Felsmann, Marika
Schindler, Diana
Weber, Edwin
author_facet Felsmann, Marika
Schindler, Diana
Weber, Edwin
author_sort Felsmann, Marika
collection PubMed
description In the title compound, C(19)H(14)N(4), which was crystallized from dimethyl sulfoxide, the arene and heterocyclic rings of the lophine analogue framework differ only slightly from coplanarity (dihedral angles range from 8.8 to 20.2°), and intramolecular N—H⋯N and C—H⋯N interactions help to establish the conformation. The crystal packing features a number of weak C—H⋯N, N—H⋯N hydrogen-bond type contacts, and C—H⋯π interactions, leading to the formation of a herringbone structure.
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spelling pubmed-29801262010-12-30 2-Phenyl-4,5-di-2-pyridyl-1H-imidazole Felsmann, Marika Schindler, Diana Weber, Edwin Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(14)N(4), which was crystallized from dimethyl sulfoxide, the arene and heterocyclic rings of the lophine analogue framework differ only slightly from coplanarity (dihedral angles range from 8.8 to 20.2°), and intramolecular N—H⋯N and C—H⋯N interactions help to establish the conformation. The crystal packing features a number of weak C—H⋯N, N—H⋯N hydrogen-bond type contacts, and C—H⋯π interactions, leading to the formation of a herringbone structure. International Union of Crystallography 2009-12-16 /pmc/articles/PMC2980126/ /pubmed/21580039 http://dx.doi.org/10.1107/S1600536809053215 Text en © Felsmann 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
Felsmann, Marika
Schindler, Diana
Weber, Edwin
2-Phenyl-4,5-di-2-pyridyl-1H-imidazole
title 2-Phenyl-4,5-di-2-pyridyl-1H-imidazole
title_full 2-Phenyl-4,5-di-2-pyridyl-1H-imidazole
title_fullStr 2-Phenyl-4,5-di-2-pyridyl-1H-imidazole
title_full_unstemmed 2-Phenyl-4,5-di-2-pyridyl-1H-imidazole
title_short 2-Phenyl-4,5-di-2-pyridyl-1H-imidazole
title_sort 2-phenyl-4,5-di-2-pyridyl-1h-imidazole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980126/
https://www.ncbi.nlm.nih.gov/pubmed/21580039
http://dx.doi.org/10.1107/S1600536809053215
work_keys_str_mv AT felsmannmarika 2phenyl45di2pyridyl1himidazole
AT schindlerdiana 2phenyl45di2pyridyl1himidazole
AT weberedwin 2phenyl45di2pyridyl1himidazole

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