2-Phenyl-5-(p-tol­yl)-1,3,4-oxadiazole

The title compound, C(15)H(12)N(2)O, adopts the expected near-planar geometry, the phenyl and tolyl rings being inclined relative to the oxadiazole ring by 3.8 (3) and 8.3 (2)°, respectively. This allows adjacent mol­ecules to pack in a parallel fashion and form stacking along [010] via π–π inter­ac...

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Autores principales: Cordes, David B., Hua, Guoxiong, Slawin, Alexandra M. Z., Woollins, J. Derek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152068/
https://www.ncbi.nlm.nih.gov/pubmed/21837139
http://dx.doi.org/10.1107/S1600536811023579
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author Cordes, David B.
Hua, Guoxiong
Slawin, Alexandra M. Z.
Woollins, J. Derek
author_facet Cordes, David B.
Hua, Guoxiong
Slawin, Alexandra M. Z.
Woollins, J. Derek
author_sort Cordes, David B.
collection PubMed
description The title compound, C(15)H(12)N(2)O, adopts the expected near-planar geometry, the phenyl and tolyl rings being inclined relative to the oxadiazole ring by 3.8 (3) and 8.3 (2)°, respectively. This allows adjacent mol­ecules to pack in a parallel fashion and form stacking along [010] via π–π inter­actions [centroid–centroid distances = 3.629 (2) and 3.723 (2) Å]. Further inter­molecular inter­actions include C—H⋯π inter­actions and weak C—H⋯N hydrogen bonds, giving rise to a crossed herringbone packing motif.
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spelling pubmed-31520682011-08-11 2-Phenyl-5-(p-tol­yl)-1,3,4-oxadiazole Cordes, David B. Hua, Guoxiong Slawin, Alexandra M. Z. Woollins, J. Derek Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(12)N(2)O, adopts the expected near-planar geometry, the phenyl and tolyl rings being inclined relative to the oxadiazole ring by 3.8 (3) and 8.3 (2)°, respectively. This allows adjacent mol­ecules to pack in a parallel fashion and form stacking along [010] via π–π inter­actions [centroid–centroid distances = 3.629 (2) and 3.723 (2) Å]. Further inter­molecular inter­actions include C—H⋯π inter­actions and weak C—H⋯N hydrogen bonds, giving rise to a crossed herringbone packing motif. International Union of Crystallography 2011-06-22 /pmc/articles/PMC3152068/ /pubmed/21837139 http://dx.doi.org/10.1107/S1600536811023579 Text en © Cordes et al. 2011 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
Cordes, David B.
Hua, Guoxiong
Slawin, Alexandra M. Z.
Woollins, J. Derek
2-Phenyl-5-(p-tol­yl)-1,3,4-oxadiazole
title 2-Phenyl-5-(p-tol­yl)-1,3,4-oxadiazole
title_full 2-Phenyl-5-(p-tol­yl)-1,3,4-oxadiazole
title_fullStr 2-Phenyl-5-(p-tol­yl)-1,3,4-oxadiazole
title_full_unstemmed 2-Phenyl-5-(p-tol­yl)-1,3,4-oxadiazole
title_short 2-Phenyl-5-(p-tol­yl)-1,3,4-oxadiazole
title_sort 2-phenyl-5-(p-tol­yl)-1,3,4-oxadiazole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152068/
https://www.ncbi.nlm.nih.gov/pubmed/21837139
http://dx.doi.org/10.1107/S1600536811023579
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