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2-Amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1)

The asymmetric unit of the title compound, 3C(5)H(6)ClN(2) (+)·3C(8)H(5)O(4) (−)·C(8)H(6)O(4), contains three independent 2-amino-5-chloro­pyridinium cations, three independent hydrogen phthal­ate anions and one phthalic acid mol­ecule. In the crystal structure, there are two kinds of supra­molecula...

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Detalles Bibliográficos
Autores principales: Hemamalini, Madhukar, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983198/
https://www.ncbi.nlm.nih.gov/pubmed/21587526
http://dx.doi.org/10.1107/S1600536810035853
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author Hemamalini, Madhukar
Fun, Hoong-Kun
author_facet Hemamalini, Madhukar
Fun, Hoong-Kun
author_sort Hemamalini, Madhukar
collection PubMed
description The asymmetric unit of the title compound, 3C(5)H(6)ClN(2) (+)·3C(8)H(5)O(4) (−)·C(8)H(6)O(4), contains three independent 2-amino-5-chloro­pyridinium cations, three independent hydrogen phthal­ate anions and one phthalic acid mol­ecule. In the crystal structure, there are two kinds of supra­molecular tapes. One is formed by two independent cations with two anions through N—H⋯O and C—H⋯O hydrogen bonds. Another one is formed by the other cation and anion, and the phthalic acid mol­ecule via N—H⋯O, O—H⋯O and C—H⋯O hydrogen bonds. These two tapes are connected by an O—H⋯O hydrogen bond, forming a double-tape structure.
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spelling pubmed-29831982010-12-30 2-Amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1) Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, 3C(5)H(6)ClN(2) (+)·3C(8)H(5)O(4) (−)·C(8)H(6)O(4), contains three independent 2-amino-5-chloro­pyridinium cations, three independent hydrogen phthal­ate anions and one phthalic acid mol­ecule. In the crystal structure, there are two kinds of supra­molecular tapes. One is formed by two independent cations with two anions through N—H⋯O and C—H⋯O hydrogen bonds. Another one is formed by the other cation and anion, and the phthalic acid mol­ecule via N—H⋯O, O—H⋯O and C—H⋯O hydrogen bonds. These two tapes are connected by an O—H⋯O hydrogen bond, forming a double-tape structure. International Union of Crystallography 2010-09-11 /pmc/articles/PMC2983198/ /pubmed/21587526 http://dx.doi.org/10.1107/S1600536810035853 Text en © Hemamalini and Fun 2010 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
Hemamalini, Madhukar
Fun, Hoong-Kun
2-Amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1)
title 2-Amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1)
title_full 2-Amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1)
title_fullStr 2-Amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1)
title_full_unstemmed 2-Amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1)
title_short 2-Amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1)
title_sort 2-amino-5-chloro­pyridinium 2-carb­oxy­benzoate–benzene-1,2-dicarb­oxy­lic acid (3/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983198/
https://www.ncbi.nlm.nih.gov/pubmed/21587526
http://dx.doi.org/10.1107/S1600536810035853
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