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4-Amino­pyridinium hydrogen succinate

In the title salt, C(5)H(7)N(2) (+)·C(4)H(5)O(4) (−), the asymmetric unit comprises an amino­pyridinium cation and a hydrogen succinate anion as protonation of the aromatic N atom of the 4-amino­pyridine mol­ecule has occurred. The crystal packing is stabilized by inter­molecular O—H⋯O and N—H⋯O hyd...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, John, Jain, Jebas, Samuel Robinson, Balasubramanian, T
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968853/
https://www.ncbi.nlm.nih.gov/pubmed/21582495
http://dx.doi.org/10.1107/S1600536809006990
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author Fun, Hoong-Kun
John, Jain
Jebas, Samuel Robinson
Balasubramanian, T
author_facet Fun, Hoong-Kun
John, Jain
Jebas, Samuel Robinson
Balasubramanian, T
author_sort Fun, Hoong-Kun
collection PubMed
description In the title salt, C(5)H(7)N(2) (+)·C(4)H(5)O(4) (−), the asymmetric unit comprises an amino­pyridinium cation and a hydrogen succinate anion as protonation of the aromatic N atom of the 4-amino­pyridine mol­ecule has occurred. The crystal packing is stabilized by inter­molecular O—H⋯O and N—H⋯O hydrogen bonds that lead to a two-dimensional array. Short C—H⋯O contacts are also present.
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spelling pubmed-29688532010-12-30 4-Amino­pyridinium hydrogen succinate Fun, Hoong-Kun John, Jain Jebas, Samuel Robinson Balasubramanian, T Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title salt, C(5)H(7)N(2) (+)·C(4)H(5)O(4) (−), the asymmetric unit comprises an amino­pyridinium cation and a hydrogen succinate anion as protonation of the aromatic N atom of the 4-amino­pyridine mol­ecule has occurred. The crystal packing is stabilized by inter­molecular O—H⋯O and N—H⋯O hydrogen bonds that lead to a two-dimensional array. Short C—H⋯O contacts are also present. International Union of Crystallography 2009-03-14 /pmc/articles/PMC2968853/ /pubmed/21582495 http://dx.doi.org/10.1107/S1600536809006990 Text en © Fun et al. 2009 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
Fun, Hoong-Kun
John, Jain
Jebas, Samuel Robinson
Balasubramanian, T
4-Amino­pyridinium hydrogen succinate
title 4-Amino­pyridinium hydrogen succinate
title_full 4-Amino­pyridinium hydrogen succinate
title_fullStr 4-Amino­pyridinium hydrogen succinate
title_full_unstemmed 4-Amino­pyridinium hydrogen succinate
title_short 4-Amino­pyridinium hydrogen succinate
title_sort 4-amino­pyridinium hydrogen succinate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968853/
https://www.ncbi.nlm.nih.gov/pubmed/21582495
http://dx.doi.org/10.1107/S1600536809006990
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AT johnjain 4aminopyridiniumhydrogensuccinate
AT jebassamuelrobinson 4aminopyridiniumhydrogensuccinate
AT balasubramaniant 4aminopyridiniumhydrogensuccinate