2-Amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate

In the crystal structure of the title compound, C(4)H(6)N(3) (+)·C(7)H(7)O(3)S(−), inter­molecular N—H⋯O hydrogen bonds link the cations and anions into chains along [100]. Additional stabilization is provided by weak C—H⋯O hydrogen bonds. An inter­molecular π–π stacking inter­action with a centroid...

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Detalles Bibliográficos
Autores principales: Tabatabaee, Masoumeh, Noozari, Najmeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120468/
https://www.ncbi.nlm.nih.gov/pubmed/21754830
http://dx.doi.org/10.1107/S1600536811018198
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author Tabatabaee, Masoumeh
Noozari, Najmeh
author_facet Tabatabaee, Masoumeh
Noozari, Najmeh
author_sort Tabatabaee, Masoumeh
collection PubMed
description In the crystal structure of the title compound, C(4)H(6)N(3) (+)·C(7)H(7)O(3)S(−), inter­molecular N—H⋯O hydrogen bonds link the cations and anions into chains along [100]. Additional stabilization is provided by weak C—H⋯O hydrogen bonds. An inter­molecular π–π stacking inter­action with a centroid–centroid distance of 3.6957 (7) Å is also observed. The H atoms of the methyl group were refined as disordered over two sets of sites with equal occupancies
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spelling pubmed-31204682011-07-13 2-Amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate Tabatabaee, Masoumeh Noozari, Najmeh Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(4)H(6)N(3) (+)·C(7)H(7)O(3)S(−), inter­molecular N—H⋯O hydrogen bonds link the cations and anions into chains along [100]. Additional stabilization is provided by weak C—H⋯O hydrogen bonds. An inter­molecular π–π stacking inter­action with a centroid–centroid distance of 3.6957 (7) Å is also observed. The H atoms of the methyl group were refined as disordered over two sets of sites with equal occupancies International Union of Crystallography 2011-05-20 /pmc/articles/PMC3120468/ /pubmed/21754830 http://dx.doi.org/10.1107/S1600536811018198 Text en © Tabatabaee and Noozari 2011 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
Tabatabaee, Masoumeh
Noozari, Najmeh
2-Amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate
title 2-Amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate
title_full 2-Amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate
title_fullStr 2-Amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate
title_full_unstemmed 2-Amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate
title_short 2-Amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate
title_sort 2-amino­pyrimidin-1-ium 4-methyl­benzene­sulfonate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120468/
https://www.ncbi.nlm.nih.gov/pubmed/21754830
http://dx.doi.org/10.1107/S1600536811018198
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AT noozarinajmeh 2aminopyrimidin1ium4methylbenzenesulfonate

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