2,5-Bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole

In the title compound, C(16)H(14)N(2)O(3), the essentially planar 1,3,4-oxadiazole ring [maximum deviation = 0.0021 (11) Å] is inclined at dihedral angles of 8.06 (6) and 11.21 (6)° with respect to the two benzene rings; the dihedral angle between the latter rings is 11.66 (5)°. In the crystal, shor...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Goh, Jia Hao, Nithinchandra, Kalluraya, B.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011497/
https://www.ncbi.nlm.nih.gov/pubmed/21589381
http://dx.doi.org/10.1107/S1600536810044405
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author Fun, Hoong-Kun
Goh, Jia Hao
Nithinchandra,
Kalluraya, B.
author_facet Fun, Hoong-Kun
Goh, Jia Hao
Nithinchandra,
Kalluraya, B.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(16)H(14)N(2)O(3), the essentially planar 1,3,4-oxadiazole ring [maximum deviation = 0.0021 (11) Å] is inclined at dihedral angles of 8.06 (6) and 11.21 (6)° with respect to the two benzene rings; the dihedral angle between the latter rings is 11.66 (5)°. In the crystal, short inter­molecular C⋯O inter­actions [2.9968 (15) Å] connect adjacent mol­ecules into chains propagating in [203]. The crystal structure is further stabilized by weak inter­molecular C—H⋯π inter­actions.
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spelling pubmed-30114972010-12-30 2,5-Bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole Fun, Hoong-Kun Goh, Jia Hao Nithinchandra, Kalluraya, B. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(14)N(2)O(3), the essentially planar 1,3,4-oxadiazole ring [maximum deviation = 0.0021 (11) Å] is inclined at dihedral angles of 8.06 (6) and 11.21 (6)° with respect to the two benzene rings; the dihedral angle between the latter rings is 11.66 (5)°. In the crystal, short inter­molecular C⋯O inter­actions [2.9968 (15) Å] connect adjacent mol­ecules into chains propagating in [203]. The crystal structure is further stabilized by weak inter­molecular C—H⋯π inter­actions. International Union of Crystallography 2010-11-06 /pmc/articles/PMC3011497/ /pubmed/21589381 http://dx.doi.org/10.1107/S1600536810044405 Text en © Fun 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
Fun, Hoong-Kun
Goh, Jia Hao
Nithinchandra,
Kalluraya, B.
2,5-Bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole
title 2,5-Bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole
title_full 2,5-Bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole
title_fullStr 2,5-Bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole
title_full_unstemmed 2,5-Bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole
title_short 2,5-Bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole
title_sort 2,5-bis(4-meth­oxy­phen­yl)-1,3,4-oxadiazole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011497/
https://www.ncbi.nlm.nih.gov/pubmed/21589381
http://dx.doi.org/10.1107/S1600536810044405
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