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Hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate
Reaction of 5-sulfosalicylic acid with hydrazine hydrate at pH = 1 results in the formation of the title hydrated salt, 0.5N(2)H(6) (2+)·C(7)H(5)O(6)S(−)·2H(2)O. The hydrazinium dications lie on centres of inversion. They are located between 3-carboxy-4-hydroxybenzenesulfonate anions, forming in...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089212/ https://www.ncbi.nlm.nih.gov/pubmed/21754532 http://dx.doi.org/10.1107/S1600536811014231 |
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author | Selvaraju, Devipriya Venkatesh, Ranjithkumar Sundararajan, Vairam |
author_facet | Selvaraju, Devipriya Venkatesh, Ranjithkumar Sundararajan, Vairam |
author_sort | Selvaraju, Devipriya |
collection | PubMed |
description | Reaction of 5-sulfosalicylic acid with hydrazine hydrate at pH = 1 results in the formation of the title hydrated salt, 0.5N(2)H(6) (2+)·C(7)H(5)O(6)S(−)·2H(2)O. The hydrazinium dications lie on centres of inversion. They are located between 3-carboxy-4-hydroxybenzenesulfonate anions, forming intermolecular N—H⋯O hydrogen bonds with sulfonate ions and water molecules of crystallisation. Further intra- and intermolecular O—H⋯O hydrogen bonds are observed in the crystal structure. |
format | Text |
id | pubmed-3089212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30892122011-07-13 Hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate Selvaraju, Devipriya Venkatesh, Ranjithkumar Sundararajan, Vairam Acta Crystallogr Sect E Struct Rep Online Organic Papers Reaction of 5-sulfosalicylic acid with hydrazine hydrate at pH = 1 results in the formation of the title hydrated salt, 0.5N(2)H(6) (2+)·C(7)H(5)O(6)S(−)·2H(2)O. The hydrazinium dications lie on centres of inversion. They are located between 3-carboxy-4-hydroxybenzenesulfonate anions, forming intermolecular N—H⋯O hydrogen bonds with sulfonate ions and water molecules of crystallisation. Further intra- and intermolecular O—H⋯O hydrogen bonds are observed in the crystal structure. International Union of Crystallography 2011-04-29 /pmc/articles/PMC3089212/ /pubmed/21754532 http://dx.doi.org/10.1107/S1600536811014231 Text en © Selvaraju 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 Selvaraju, Devipriya Venkatesh, Ranjithkumar Sundararajan, Vairam Hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate |
title | Hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate |
title_full | Hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate |
title_fullStr | Hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate |
title_full_unstemmed | Hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate |
title_short | Hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate |
title_sort | hydrazine-1,2-diium bis(3-carboxy-4-hydroxybenzenesulfonate) tetrahydrate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089212/ https://www.ncbi.nlm.nih.gov/pubmed/21754532 http://dx.doi.org/10.1107/S1600536811014231 |
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