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3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate
The title structure, C(15)H(7)N(7)O(10)·C(3)H(6)O, was prepared by pentanitration of 3,5-diphenyl-1H-pyrazole. The proton attached to a pyrazole N atom forms a hydrogen bond with the O atom of the acetone solvent molecule, owing to the NO(2) enhanced acidity of the proton. The NO(2) group on the p...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275082/ https://www.ncbi.nlm.nih.gov/pubmed/22347027 http://dx.doi.org/10.1107/S1600536812001146 |
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author | Mathivathanan, Logesh |
author_facet | Mathivathanan, Logesh |
author_sort | Mathivathanan, Logesh |
collection | PubMed |
description | The title structure, C(15)H(7)N(7)O(10)·C(3)H(6)O, was prepared by pentanitration of 3,5-diphenyl-1H-pyrazole. The proton attached to a pyrazole N atom forms a hydrogen bond with the O atom of the acetone solvent molecule, owing to the NO(2) enhanced acidity of the proton. The NO(2) group on the phenyl C atom is twisted by 33.9 (2)° from coplanarity with the ring in order to avoid a short intramolecular O⋯O contact with an O atom of an adjacent pyrazole-bonded NO(2) group. |
format | Online Article Text |
id | pubmed-3275082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32750822012-02-15 3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate Mathivathanan, Logesh Acta Crystallogr Sect E Struct Rep Online Organic Papers The title structure, C(15)H(7)N(7)O(10)·C(3)H(6)O, was prepared by pentanitration of 3,5-diphenyl-1H-pyrazole. The proton attached to a pyrazole N atom forms a hydrogen bond with the O atom of the acetone solvent molecule, owing to the NO(2) enhanced acidity of the proton. The NO(2) group on the phenyl C atom is twisted by 33.9 (2)° from coplanarity with the ring in order to avoid a short intramolecular O⋯O contact with an O atom of an adjacent pyrazole-bonded NO(2) group. International Union of Crystallography 2012-01-14 /pmc/articles/PMC3275082/ /pubmed/22347027 http://dx.doi.org/10.1107/S1600536812001146 Text en © Logesh Mathivathanan 2012 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 Mathivathanan, Logesh 3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate |
title | 3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate |
title_full | 3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate |
title_fullStr | 3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate |
title_full_unstemmed | 3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate |
title_short | 3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate |
title_sort | 3,5-bis(2,4-dinitrophenyl)-4-nitro-1h-pyrazole acetone monosolvate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275082/ https://www.ncbi.nlm.nih.gov/pubmed/22347027 http://dx.doi.org/10.1107/S1600536812001146 |
work_keys_str_mv | AT mathivathananlogesh 35bis24dinitrophenyl4nitro1hpyrazoleacetonemonosolvate |