2-(Aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate

In the crystal structure of the title proton-transfer compound, CH(6)N(3)O(+)·C(7)H(4)NO(4) (−), O—H⋯O and N—H⋯O hydrogen bonds are formed respectively between the cations and the anions, each component affording a supra­molecular chain along the c axis. The cation and anion chains are further linke...

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Detalles Bibliográficos
Autores principales: Idrees, Mohammad, Shadab, Shah Mohammad, Kumar, Sarvendra
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969516/
https://www.ncbi.nlm.nih.gov/pubmed/21582793
http://dx.doi.org/10.1107/S1600536809020601
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author Idrees, Mohammad
Shadab, Shah Mohammad
Kumar, Sarvendra
author_facet Idrees, Mohammad
Shadab, Shah Mohammad
Kumar, Sarvendra
author_sort Idrees, Mohammad
collection PubMed
description In the crystal structure of the title proton-transfer compound, CH(6)N(3)O(+)·C(7)H(4)NO(4) (−), O—H⋯O and N—H⋯O hydrogen bonds are formed respectively between the cations and the anions, each component affording a supra­molecular chain along the c axis. The cation and anion chains are further linked by N—H⋯O and N—H⋯N hydrogen bonds. A π–π inter­action is also observed between the pyridine rings; the inter­planar separation and the centroid–centroid distance are 3.3425 (6) and 4.6256 (11) Å, respectively.
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spelling pubmed-29695162010-12-30 2-(Aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate Idrees, Mohammad Shadab, Shah Mohammad Kumar, Sarvendra Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title proton-transfer compound, CH(6)N(3)O(+)·C(7)H(4)NO(4) (−), O—H⋯O and N—H⋯O hydrogen bonds are formed respectively between the cations and the anions, each component affording a supra­molecular chain along the c axis. The cation and anion chains are further linked by N—H⋯O and N—H⋯N hydrogen bonds. A π–π inter­action is also observed between the pyridine rings; the inter­planar separation and the centroid–centroid distance are 3.3425 (6) and 4.6256 (11) Å, respectively. International Union of Crystallography 2009-06-06 /pmc/articles/PMC2969516/ /pubmed/21582793 http://dx.doi.org/10.1107/S1600536809020601 Text en © Idrees 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
Idrees, Mohammad
Shadab, Shah Mohammad
Kumar, Sarvendra
2-(Aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate
title 2-(Aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate
title_full 2-(Aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate
title_fullStr 2-(Aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate
title_full_unstemmed 2-(Aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate
title_short 2-(Aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate
title_sort 2-(aminocarbonyl)hydrazin-1-ium 6-carboxy­picolinate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969516/
https://www.ncbi.nlm.nih.gov/pubmed/21582793
http://dx.doi.org/10.1107/S1600536809020601
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