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N′-(4-Fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide
In the title compound, C(15)H(12)F(2)N(2)O, the dihedral angle between the two benzene rings is 48.73 (8)°. The hydrazine group is twisted slightly, with a C—N—N—C torsion angle of 172.48 (12)°. In the crystal, molecules are connected by strong N—H⋯O and weak C—H⋯O hydrogen bonds, forming supramol...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247574/ https://www.ncbi.nlm.nih.gov/pubmed/22219879 http://dx.doi.org/10.1107/S1600536811039845 |
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author | Fun, Hoong-Kun Hemamalini, Madhukar Sumangala, V. Nagaraja, G. K. Poojary, Boja |
author_facet | Fun, Hoong-Kun Hemamalini, Madhukar Sumangala, V. Nagaraja, G. K. Poojary, Boja |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | In the title compound, C(15)H(12)F(2)N(2)O, the dihedral angle between the two benzene rings is 48.73 (8)°. The hydrazine group is twisted slightly, with a C—N—N—C torsion angle of 172.48 (12)°. In the crystal, molecules are connected by strong N—H⋯O and weak C—H⋯O hydrogen bonds, forming supramolecular chains along the c axis. The structure is consolidated by π–π [centroid–centroid separation = 3.6579 (10) Å] and C—H⋯π interactions. |
format | Online Article Text |
id | pubmed-3247574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32475742012-01-04 N′-(4-Fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide Fun, Hoong-Kun Hemamalini, Madhukar Sumangala, V. Nagaraja, G. K. Poojary, Boja Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(12)F(2)N(2)O, the dihedral angle between the two benzene rings is 48.73 (8)°. The hydrazine group is twisted slightly, with a C—N—N—C torsion angle of 172.48 (12)°. In the crystal, molecules are connected by strong N—H⋯O and weak C—H⋯O hydrogen bonds, forming supramolecular chains along the c axis. The structure is consolidated by π–π [centroid–centroid separation = 3.6579 (10) Å] and C—H⋯π interactions. International Union of Crystallography 2011-10-05 /pmc/articles/PMC3247574/ /pubmed/22219879 http://dx.doi.org/10.1107/S1600536811039845 Text en © Fun 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 Fun, Hoong-Kun Hemamalini, Madhukar Sumangala, V. Nagaraja, G. K. Poojary, Boja N′-(4-Fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide |
title |
N′-(4-Fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide |
title_full |
N′-(4-Fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide |
title_fullStr |
N′-(4-Fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide |
title_full_unstemmed |
N′-(4-Fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide |
title_short |
N′-(4-Fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide |
title_sort | n′-(4-fluorobenzylidene)-2-(4-fluorophenyl)acetohydrazide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247574/ https://www.ncbi.nlm.nih.gov/pubmed/22219879 http://dx.doi.org/10.1107/S1600536811039845 |
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