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Piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate

The title solvated molecular salt, C(4)H(12)N(2) (2+)·C(7)H(3)NO(4) (2−)·CH(3)OH or (pipzH(2))(py-2,3-dc)·MeOH, was prepared by the reaction of pyridine-2,3-dicarb­oxy­lic acid (py-2,3-dcH(2)) and piperazine (pipz) in methanol (MeOH) as solvent. One of the two carboxylate groups of the acid fragment...

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Detalles Bibliográficos
Autores principales: Manteghi, Faranak, Ghadermazi, Mohammad, Kakaei, Nasrin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089228/
https://www.ncbi.nlm.nih.gov/pubmed/21754436
http://dx.doi.org/10.1107/S1600536811012384
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author Manteghi, Faranak
Ghadermazi, Mohammad
Kakaei, Nasrin
author_facet Manteghi, Faranak
Ghadermazi, Mohammad
Kakaei, Nasrin
author_sort Manteghi, Faranak
collection PubMed
description The title solvated molecular salt, C(4)H(12)N(2) (2+)·C(7)H(3)NO(4) (2−)·CH(3)OH or (pipzH(2))(py-2,3-dc)·MeOH, was prepared by the reaction of pyridine-2,3-dicarb­oxy­lic acid (py-2,3-dcH(2)) and piperazine (pipz) in methanol (MeOH) as solvent. One of the two carboxylate groups of the acid fragment is nearly perpendicular to the pyridine ring and the other is almost in its plane [C—C—C—O torsion angles = −85.50 (11) and 88.07 (11)° and N—C—C—O torsion angles = −176.31 (8) and 5.41 (13)°]. In the crystal, the components are linked by O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds, generating a three-dimensional network.
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spelling pubmed-30892282011-07-13 Piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate Manteghi, Faranak Ghadermazi, Mohammad Kakaei, Nasrin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title solvated molecular salt, C(4)H(12)N(2) (2+)·C(7)H(3)NO(4) (2−)·CH(3)OH or (pipzH(2))(py-2,3-dc)·MeOH, was prepared by the reaction of pyridine-2,3-dicarb­oxy­lic acid (py-2,3-dcH(2)) and piperazine (pipz) in methanol (MeOH) as solvent. One of the two carboxylate groups of the acid fragment is nearly perpendicular to the pyridine ring and the other is almost in its plane [C—C—C—O torsion angles = −85.50 (11) and 88.07 (11)° and N—C—C—O torsion angles = −176.31 (8) and 5.41 (13)°]. In the crystal, the components are linked by O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds, generating a three-dimensional network. International Union of Crystallography 2011-04-13 /pmc/articles/PMC3089228/ /pubmed/21754436 http://dx.doi.org/10.1107/S1600536811012384 Text en © Manteghi et al. 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
Manteghi, Faranak
Ghadermazi, Mohammad
Kakaei, Nasrin
Piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate
title Piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate
title_full Piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate
title_fullStr Piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate
title_full_unstemmed Piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate
title_short Piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate
title_sort piperazine-1,4-diium pyridine-2,3-dicarboxyl­ate methanol monosolvate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089228/
https://www.ncbi.nlm.nih.gov/pubmed/21754436
http://dx.doi.org/10.1107/S1600536811012384
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