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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...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2011
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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. |
format | Text |
id | pubmed-3089228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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
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title_full | Piperazine-1,4-diium pyridine-2,3-dicarboxylate methanol monosolvate
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title_fullStr | Piperazine-1,4-diium pyridine-2,3-dicarboxylate methanol monosolvate
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title_full_unstemmed | Piperazine-1,4-diium pyridine-2,3-dicarboxylate methanol monosolvate
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title_short | Piperazine-1,4-diium pyridine-2,3-dicarboxylate methanol monosolvate
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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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