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Hydrogen 4-ammonio­phenyl­phospho­n­ate

The title compound, C(6)H(8)NO(3)P, is isostructural with p-arsanilic acid. It exists as the zwitterion H(3)N(+)C(6)H(4)PO(3)H(−). In the crystal, mol­ecules are linked by O—H⋯O and N—H⋯O hydrogen-bond bridges, giving a three-dimensional network structure. The strongest hydrogen bonds are formed bet...

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Detalles Bibliográficos
Autores principales: Thiele, Kerstin, Wagner, Christoph, Merzweiler, Kurt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274954/
https://www.ncbi.nlm.nih.gov/pubmed/22346907
http://dx.doi.org/10.1107/S1600536811055218
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author Thiele, Kerstin
Wagner, Christoph
Merzweiler, Kurt
author_facet Thiele, Kerstin
Wagner, Christoph
Merzweiler, Kurt
author_sort Thiele, Kerstin
collection PubMed
description The title compound, C(6)H(8)NO(3)P, is isostructural with p-arsanilic acid. It exists as the zwitterion H(3)N(+)C(6)H(4)PO(3)H(−). In the crystal, mol­ecules are linked by O—H⋯O and N—H⋯O hydrogen-bond bridges, giving a three-dimensional network structure. The strongest hydrogen bonds are formed between adjacent PO(3)H groups with O⋯O distances of 2.577 (2) Å.
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spelling pubmed-32749542012-02-15 Hydrogen 4-ammonio­phenyl­phospho­n­ate Thiele, Kerstin Wagner, Christoph Merzweiler, Kurt Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(6)H(8)NO(3)P, is isostructural with p-arsanilic acid. It exists as the zwitterion H(3)N(+)C(6)H(4)PO(3)H(−). In the crystal, mol­ecules are linked by O—H⋯O and N—H⋯O hydrogen-bond bridges, giving a three-dimensional network structure. The strongest hydrogen bonds are formed between adjacent PO(3)H groups with O⋯O distances of 2.577 (2) Å. International Union of Crystallography 2012-01-07 /pmc/articles/PMC3274954/ /pubmed/22346907 http://dx.doi.org/10.1107/S1600536811055218 Text en © Thiele 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
Thiele, Kerstin
Wagner, Christoph
Merzweiler, Kurt
Hydrogen 4-ammonio­phenyl­phospho­n­ate
title Hydrogen 4-ammonio­phenyl­phospho­n­ate
title_full Hydrogen 4-ammonio­phenyl­phospho­n­ate
title_fullStr Hydrogen 4-ammonio­phenyl­phospho­n­ate
title_full_unstemmed Hydrogen 4-ammonio­phenyl­phospho­n­ate
title_short Hydrogen 4-ammonio­phenyl­phospho­n­ate
title_sort hydrogen 4-ammonio­phenyl­phospho­n­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274954/
https://www.ncbi.nlm.nih.gov/pubmed/22346907
http://dx.doi.org/10.1107/S1600536811055218
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