1-Ammonio-1-phosphono­pentane-1-phospho­nic acid

The title compound, C(5)H(15)NO(6)P(2), was obtained by the reaction of penta­nenitrile with PCl(3) followed by the dropwise addition of water. The asymmetric unit contains one mol­ecule, which exists as a zwitterion with a positive charge on the –NH(3) group and a negative charge on one of the phos...

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Detalles Bibliográficos
Autores principales: Bon, V. V., Dudko, A. V., Kozachkova, A. N., Pekhnyo, V. I.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959911/
https://www.ncbi.nlm.nih.gov/pubmed/21581404
http://dx.doi.org/10.1107/S1600536808038968
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author Bon, V. V.
Dudko, A. V.
Kozachkova, A. N.
Pekhnyo, V. I.
author_facet Bon, V. V.
Dudko, A. V.
Kozachkova, A. N.
Pekhnyo, V. I.
author_sort Bon, V. V.
collection PubMed
description The title compound, C(5)H(15)NO(6)P(2), was obtained by the reaction of penta­nenitrile with PCl(3) followed by the dropwise addition of water. The asymmetric unit contains one mol­ecule, which exists as a zwitterion with a positive charge on the –NH(3) group and a negative charge on one of the phospho­nic O atoms. The crystal structure displays N—H⋯O and O—H⋯O hydrogen bonding, which creates a three-dimensional network.
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spelling pubmed-29599112010-12-30 1-Ammonio-1-phosphono­pentane-1-phospho­nic acid Bon, V. V. Dudko, A. V. Kozachkova, A. N. Pekhnyo, V. I. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(5)H(15)NO(6)P(2), was obtained by the reaction of penta­nenitrile with PCl(3) followed by the dropwise addition of water. The asymmetric unit contains one mol­ecule, which exists as a zwitterion with a positive charge on the –NH(3) group and a negative charge on one of the phospho­nic O atoms. The crystal structure displays N—H⋯O and O—H⋯O hydrogen bonding, which creates a three-dimensional network. International Union of Crystallography 2008-11-26 /pmc/articles/PMC2959911/ /pubmed/21581404 http://dx.doi.org/10.1107/S1600536808038968 Text en © Bon et al. 2008 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
Bon, V. V.
Dudko, A. V.
Kozachkova, A. N.
Pekhnyo, V. I.
1-Ammonio-1-phosphono­pentane-1-phospho­nic acid
title 1-Ammonio-1-phosphono­pentane-1-phospho­nic acid
title_full 1-Ammonio-1-phosphono­pentane-1-phospho­nic acid
title_fullStr 1-Ammonio-1-phosphono­pentane-1-phospho­nic acid
title_full_unstemmed 1-Ammonio-1-phosphono­pentane-1-phospho­nic acid
title_short 1-Ammonio-1-phosphono­pentane-1-phospho­nic acid
title_sort 1-ammonio-1-phosphono­pentane-1-phospho­nic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959911/
https://www.ncbi.nlm.nih.gov/pubmed/21581404
http://dx.doi.org/10.1107/S1600536808038968
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AT dudkoav 1ammonio1phosphonopentane1phosphonicacid
AT kozachkovaan 1ammonio1phosphonopentane1phosphonicacid
AT pekhnyovi 1ammonio1phosphonopentane1phosphonicacid

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