Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxylate tetrahydrate: a synchrotron radiation study

The title compound, 2C3H7N6+·C6H2N2O42−·4H2O or (tataH)2(pzdc)·4H2O, was synthesised by a reaction between pyrazine-2,3-dicarboxylic acid (H2pzdc) as a proton donor and 2,4,6-triamino-1,3,5-triazin (tata) as a proton acceptor. In the crystal struc...

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Main Authors: Hossein Eshtiagh-Hosseini, Azam Hassanpoor, Laura Canadillas-Delgado, Masoud Mirzaei
Format: Article
Language:English
Published: International Union of Crystallography 2010-06-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536810017290
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author Hossein Eshtiagh-Hosseini
Azam Hassanpoor
Laura Canadillas-Delgado
Masoud Mirzaei
author_facet Hossein Eshtiagh-Hosseini
Azam Hassanpoor
Laura Canadillas-Delgado
Masoud Mirzaei
author_sort Hossein Eshtiagh-Hosseini
collection DOAJ
description The title compound, 2C3H7N6+·C6H2N2O42−·4H2O or (tataH)2(pzdc)·4H2O, was synthesised by a reaction between pyrazine-2,3-dicarboxylic acid (H2pzdc) as a proton donor and 2,4,6-triamino-1,3,5-triazin (tata) as a proton acceptor. In the crystal structure, an extensive series of O—H...O, O—H...N, N—H...O and N—H...N hydrogen bonds generates a three-dimensional framework with the hydrogen bonding involving most donor and acceptor centers. π–π stacking interactions are also observed between adjacent triazine rings, with centroid–centroid distances of 3.4994 (8) and 3.5922 (7) Å.
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spelling doaj.art-aad30c80fba1464f817dad81554647162022-12-21T17:23:29ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682010-06-01666o1368o136910.1107/S1600536810017290Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxylate tetrahydrate: a synchrotron radiation studyHossein Eshtiagh-HosseiniAzam HassanpoorLaura Canadillas-DelgadoMasoud MirzaeiThe title compound, 2C3H7N6+·C6H2N2O42−·4H2O or (tataH)2(pzdc)·4H2O, was synthesised by a reaction between pyrazine-2,3-dicarboxylic acid (H2pzdc) as a proton donor and 2,4,6-triamino-1,3,5-triazin (tata) as a proton acceptor. In the crystal structure, an extensive series of O—H...O, O—H...N, N—H...O and N—H...N hydrogen bonds generates a three-dimensional framework with the hydrogen bonding involving most donor and acceptor centers. π–π stacking interactions are also observed between adjacent triazine rings, with centroid–centroid distances of 3.4994 (8) and 3.5922 (7) Å.http://scripts.iucr.org/cgi-bin/paper?S1600536810017290
spellingShingle Hossein Eshtiagh-Hosseini
Azam Hassanpoor
Laura Canadillas-Delgado
Masoud Mirzaei
Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxylate tetrahydrate: a synchrotron radiation study
Acta Crystallographica Section E
title Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxylate tetrahydrate: a synchrotron radiation study
title_full Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxylate tetrahydrate: a synchrotron radiation study
title_fullStr Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxylate tetrahydrate: a synchrotron radiation study
title_full_unstemmed Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxylate tetrahydrate: a synchrotron radiation study
title_short Bis(2,4,6-triamino-1,3,5-triazin-1-ium) pyrazine-2,3-dicarboxylate tetrahydrate: a synchrotron radiation study
title_sort bis 2 4 6 triamino 1 3 5 triazin 1 ium pyrazine 2 3 dicarboxylate tetrahydrate a synchrotron radiation study
url http://scripts.iucr.org/cgi-bin/paper?S1600536810017290
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