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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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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. |
format | Online Article Text |
id | pubmed-3274954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT thielekerstin hydrogen4ammoniophenylphosphonate AT wagnerchristoph hydrogen4ammoniophenylphosphonate AT merzweilerkurt hydrogen4ammoniophenylphosphonate |