

A new three dimensional proton transfer compound including citric acid and 2,4,6-triamine-1,3,5-triazine: synthesis, characterization and X-ray crystal structure
Hossein Eshtiagh-Hosseini (1,*)





(1) Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad, 917791436, Mashhad, Iran
(2) Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad, 917791436, Mashhad, Iran
(3) Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad, 917791436, Mashhad, Iran
(4) Department of Chemistry, University of Fribourg, Chemin du Musée 9, CH-1700 Fribourg, Switzerland
(5) Department of Chemistry, University of Fribourg, Chemin du Musée 9, CH-1700 Fribourg, Switzerland
(*) Corresponding Author
Received: 07 Apr 2010 | Revised: 18 Jul 2010 | Accepted: 04 Aug 2010 | Published: 29 Sep 2010 | Issue Date: September 2010
Abstract
A new three dimensional proton transfer compound, (tataH)2(citH).2H2O (I) was synthesized from the reaction of citric acid (citH3), and 2,4,6-triamino-1,3,5-triazine (tata). The characterization was performed using elemental analysis, IR spectroscopy, and single crystal X-ray structure determination. The crystal structure of the title compound consists of bis-2,4,6-triamino-1,3,5-triazin-1-ium cations, hydrogen citrate, and lattice water molecules. Intermolecular O-H•••O, N-H•••O, and N-H•••N hydrogen bonding interactions stabilize the crystal structure. The hydrogen bonds distances range from of 1.781 to 2.088 Å. The π-π stacking (centroid-centroid ranges 3.410-3.504 Å) between two aromatic rings of tata moieties can play an essential role in the creation and stabilization of the title crystalline network.
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European Journal of Chemistry
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DOI: 10.5155/eurjchem.1.3.179-181.44
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Ferdowsi University of Mashhad, Mashhad, Iran
Citations
[1]. Shouwen Jin, Li Liu, Daqi Wang, Jianzhong Guo
Hydrogen bonded supramolecular network in organic acid–base salts: Crystal structures of five proton-transfer complexes assembled from 5,7-dimethyl-1,8-naphthyridine-2-amine with monocarboxylic acid, dicarboxylic acid, and tricarboxylic acid
Journal of Molecular Structure 1005(1-3), 59, 2011
DOI: 10.1016/j.molstruc.2011.08.018

[2]. M. Mirzaei, H. Eshtiagh-Hosseini, N. Alfi, H. Aghabozorg, J. Attar Gharamaleki, S. A. Beyramabadi, H. R. Khavasi, A. R. Salimi, A. Shokrollahi, R. Aghaei, E. Karami
Syntheses, crystal, molecular structures, and solution studies of Cu(II), Co(II), and Zn(II) coordination compounds containing pyridine-2,6-dicarboxylic acid and 1,4-pyrazine-2,3-dicarboxylic acid: comparative computational studies of Cu(II) and Zn(II) complexes
Structural Chemistry 22(6), 1365, 2011
DOI: 10.1007/s11224-011-9829-5

[3]. Shouwen Jin, Daqi Wang, Yanfei Huang, Hao Fang, Tianyi Wang, Peixia Fu, Liangliang Ding
Hydrogen bonded supramolecular framework in organic acid–base adducts: Crystal structures of five cocrystals/salts assembled from 2-methylquinoline with monocarboxylic acid, dicarboxylic acid, and tricarboxylic acid
Journal of Molecular Structure 1017, 51, 2012
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DOI Link: https://doi.org/10.5155/eurjchem.1.3.179-181.44

















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