(2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide

In the title compound, C(16)H(13)N(3)O(4), the dihedral angle between the terminal benzene rings is 14.02 (7)°. The carbonyl groups are anti with respect to each other, which facilitates their participation in the formation of supra­molecular chains. Each side of the –C(=O)N(H)N(H)C(=O)– residue ass...

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Detalles Bibliográficos
Autores principales: Carvalho, Samir A., da Silva, Edson F., de Souza, Marcus V. N., Tiekink, Edward R. T., Wardell, James L., Wardell, Solange M. S. V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980068/
https://www.ncbi.nlm.nih.gov/pubmed/21580041
http://dx.doi.org/10.1107/S1600536809053379
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author Carvalho, Samir A.
da Silva, Edson F.
de Souza, Marcus V. N.
Tiekink, Edward R. T.
Wardell, James L.
Wardell, Solange M. S. V.
author_facet Carvalho, Samir A.
da Silva, Edson F.
de Souza, Marcus V. N.
Tiekink, Edward R. T.
Wardell, James L.
Wardell, Solange M. S. V.
author_sort Carvalho, Samir A.
collection PubMed
description In the title compound, C(16)H(13)N(3)O(4), the dihedral angle between the terminal benzene rings is 14.02 (7)°. The carbonyl groups are anti with respect to each other, which facilitates their participation in the formation of supra­molecular chains. Each side of the –C(=O)N(H)N(H)C(=O)– residue associates with a centrosymmetrically related mol­ecule, resulting in the formation of essentially flat ten-membered {⋯O=CNN(H)}(2) synthons. The resultant chains are further consolidated in the crystal structure via C—H⋯O contacts.
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spelling pubmed-29800682010-12-30 (2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide Carvalho, Samir A. da Silva, Edson F. de Souza, Marcus V. N. Tiekink, Edward R. T. Wardell, James L. Wardell, Solange M. S. V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(13)N(3)O(4), the dihedral angle between the terminal benzene rings is 14.02 (7)°. The carbonyl groups are anti with respect to each other, which facilitates their participation in the formation of supra­molecular chains. Each side of the –C(=O)N(H)N(H)C(=O)– residue associates with a centrosymmetrically related mol­ecule, resulting in the formation of essentially flat ten-membered {⋯O=CNN(H)}(2) synthons. The resultant chains are further consolidated in the crystal structure via C—H⋯O contacts. International Union of Crystallography 2009-12-16 /pmc/articles/PMC2980068/ /pubmed/21580041 http://dx.doi.org/10.1107/S1600536809053379 Text en © Carvalho 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
Carvalho, Samir A.
da Silva, Edson F.
de Souza, Marcus V. N.
Tiekink, Edward R. T.
Wardell, James L.
Wardell, Solange M. S. V.
(2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide
title (2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide
title_full (2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide
title_fullStr (2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide
title_full_unstemmed (2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide
title_short (2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide
title_sort (2e)-n′-benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980068/
https://www.ncbi.nlm.nih.gov/pubmed/21580041
http://dx.doi.org/10.1107/S1600536809053379
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