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4-Nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1)

In the title adduct, 2C(6)H(5)NO(3)·C(3)H(6)N(6)·H(2)O, the melamine and the two independent nitrophenol molecules are essentially planar, with maximum deviations of 0.0294 (10), 0.0706 (12) and 0.0742 (12) Å, respectively. In the crystal, N—H⋯N, O—H⋯N, N—H⋯O and O—H⋯O hydrogen bonds link the compon...

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Autores principales: Kanagathara, N., Chakkaravarthi, G., Marchewka, M. K., Gunasekaran, S., Anbalagan, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394065/
https://www.ncbi.nlm.nih.gov/pubmed/22798930
http://dx.doi.org/10.1107/S1600536812029066
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author Kanagathara, N.
Chakkaravarthi, G.
Marchewka, M. K.
Gunasekaran, S.
Anbalagan, G.
author_facet Kanagathara, N.
Chakkaravarthi, G.
Marchewka, M. K.
Gunasekaran, S.
Anbalagan, G.
author_sort Kanagathara, N.
collection PubMed
description In the title adduct, 2C(6)H(5)NO(3)·C(3)H(6)N(6)·H(2)O, the melamine and the two independent nitrophenol molecules are essentially planar, with maximum deviations of 0.0294 (10), 0.0706 (12) and 0.0742 (12) Å, respectively. In the crystal, N—H⋯N, O—H⋯N, N—H⋯O and O—H⋯O hydrogen bonds link the components into a three-dimensional network. In addition, weak π–π inter­actions [centroid–centroid distances = 3.728 (3) and 3.749 (3) Å] are observed.
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spelling pubmed-33940652012-07-13 4-Nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1) Kanagathara, N. Chakkaravarthi, G. Marchewka, M. K. Gunasekaran, S. Anbalagan, G. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title adduct, 2C(6)H(5)NO(3)·C(3)H(6)N(6)·H(2)O, the melamine and the two independent nitrophenol molecules are essentially planar, with maximum deviations of 0.0294 (10), 0.0706 (12) and 0.0742 (12) Å, respectively. In the crystal, N—H⋯N, O—H⋯N, N—H⋯O and O—H⋯O hydrogen bonds link the components into a three-dimensional network. In addition, weak π–π inter­actions [centroid–centroid distances = 3.728 (3) and 3.749 (3) Å] are observed. International Union of Crystallography 2012-06-30 /pmc/articles/PMC3394065/ /pubmed/22798930 http://dx.doi.org/10.1107/S1600536812029066 Text en © Kanagathara et al. 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
Kanagathara, N.
Chakkaravarthi, G.
Marchewka, M. K.
Gunasekaran, S.
Anbalagan, G.
4-Nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1)
title 4-Nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1)
title_full 4-Nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1)
title_fullStr 4-Nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1)
title_full_unstemmed 4-Nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1)
title_short 4-Nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1)
title_sort 4-nitro­phenol–2,4,6-triamino-1,3,5-triazine–water (2/1/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394065/
https://www.ncbi.nlm.nih.gov/pubmed/22798930
http://dx.doi.org/10.1107/S1600536812029066
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