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Crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate

The title salts, C(8)H(13)N(4) (+)·Cl(−), (I), and C(8)H(13)N(4) (+)·NO(3) (−), (II), contain linked pyridinium–piperazine heterocycles. In both salts, the piperazine ring adopts a chair conformation with protonation at the N atom not linked to the other ring. In the crystal of (I), weak N—H⋯Cl inte...

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Autores principales: Yamuna, Thammarse S., Jasinski, Jerry P., Kaur, Manpreet, Anderson, Brian J., Yathirajan, H. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257175/
https://www.ncbi.nlm.nih.gov/pubmed/25484652
http://dx.doi.org/10.1107/S1600536814020169
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author Yamuna, Thammarse S.
Jasinski, Jerry P.
Kaur, Manpreet
Anderson, Brian J.
Yathirajan, H. S.
author_facet Yamuna, Thammarse S.
Jasinski, Jerry P.
Kaur, Manpreet
Anderson, Brian J.
Yathirajan, H. S.
author_sort Yamuna, Thammarse S.
collection PubMed
description The title salts, C(8)H(13)N(4) (+)·Cl(−), (I), and C(8)H(13)N(4) (+)·NO(3) (−), (II), contain linked pyridinium–piperazine heterocycles. In both salts, the piperazine ring adopts a chair conformation with protonation at the N atom not linked to the other ring. In the crystal of (I), weak N—H⋯Cl inter­actions are observed, leading to zigzag chains along [100]. In the crystal of (II), both H atoms on the NH(2) (+) group form bifurcated N—H⋯(O,O) hydrogen bonds. Weak C—H⋯O inter­actions are also observed. These bonds collectively link the components into infinite chains along [100].
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spelling pubmed-42571752014-12-05 Crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate Yamuna, Thammarse S. Jasinski, Jerry P. Kaur, Manpreet Anderson, Brian J. Yathirajan, H. S. Acta Crystallogr Sect E Struct Rep Online Research Communications The title salts, C(8)H(13)N(4) (+)·Cl(−), (I), and C(8)H(13)N(4) (+)·NO(3) (−), (II), contain linked pyridinium–piperazine heterocycles. In both salts, the piperazine ring adopts a chair conformation with protonation at the N atom not linked to the other ring. In the crystal of (I), weak N—H⋯Cl inter­actions are observed, leading to zigzag chains along [100]. In the crystal of (II), both H atoms on the NH(2) (+) group form bifurcated N—H⋯(O,O) hydrogen bonds. Weak C—H⋯O inter­actions are also observed. These bonds collectively link the components into infinite chains along [100]. International Union of Crystallography 2014-09-13 /pmc/articles/PMC4257175/ /pubmed/25484652 http://dx.doi.org/10.1107/S1600536814020169 Text en © Yamuna et al. 2014 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 Research Communications
Yamuna, Thammarse S.
Jasinski, Jerry P.
Kaur, Manpreet
Anderson, Brian J.
Yathirajan, H. S.
Crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate
title Crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate
title_full Crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate
title_fullStr Crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate
title_full_unstemmed Crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate
title_short Crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate
title_sort crystal structures of 4-(pyrimidin-2-yl)piperazin-1-ium chloride and 4-(pyrimidin-2-yl)piperazin-1-ium nitrate
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4257175/
https://www.ncbi.nlm.nih.gov/pubmed/25484652
http://dx.doi.org/10.1107/S1600536814020169
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