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Crystal structures of 2-amino-pyridine citric acid salts: C 5 H 7 N 2 + ·C 6 H 7 O 7 - and 3C 5 H 7 N 2 + ·C 6 H 5 O 7 3 .
- Source :
-
Acta crystallographica. Section E, Crystallographic communications [Acta Crystallogr E Crystallogr Commun] 2018 Jul 17; Vol. 74 (Pt 8), pp. 1111-1116. Date of Electronic Publication: 2018 Jul 17 (Print Publication: 2018). - Publication Year :
- 2018
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Abstract
- 2-Amino-pyridine and citric acid mixed in 1:1 and 3:1 ratios in ethanol yielded crystals of two 2-amino-pyridinium citrate salts, viz . C <subscript>5</subscript> H <subscript>7</subscript> N <subscript>2</subscript> <superscript>+</superscript> ·C <subscript>6</subscript> H <subscript>7</subscript> O <subscript>7</subscript> <superscript>-</superscript> ( I ) (systematic name: 2-amino-pyridin-1-ium 3-carb-oxy-2-carb-oxy-methyl-2-hy-droxy-propano-ate), and 3C <subscript>5</subscript> H <subscript>7</subscript> N <subscript>2</subscript> <superscript>+</superscript> ·C <subscript>6</subscript> H <subscript>5</subscript> O <subscript>7</subscript> <superscript>3-</superscript> ( II ) [systematic name: tris-(2-amino-pyridin-1-ium) 2-hy-droxy-propane-1,2,3-tri-carboxyl-ate]. The supra-molecular synthons present are analysed and their effect upon the crystal packing is presented in the context of crystal engineering. Salt I is formed by the protonation of the pyridine N atom and deprotonation of the central carb-oxy-lic group of citric acid, while in II all three carb-oxy-lic groups of the acid are deprotonated and the charges are compensated for by three 2-amino-pyridinium cations. In both structures, a complex supra-molecular three-dimensional architecture is formed. In I , the supra-molecular aggregation results from N <subscript>amino</subscript> -H⋯O <subscript>acid</subscript> , O <subscript>acid</subscript> ⋯H-O <subscript>acid</subscript> , O <subscript>alcohol</subscript> -H⋯O <subscript>acid</subscript> , N <subscript>amino</subscript> -H⋯O <subscript>alcohol</subscript> , N <subscript>py</subscript> -H⋯O <subscript>alcohol</subscript> and C <subscript>ar</subscript> -H⋯O <subscript>acid</subscript> inter-actions. The mol-ecular conformation of the citrate ion (CA <superscript>3-</superscript> ) in II is stabilized by an intra-molecular O <subscript>alcohol</subscript> -H⋯O <subscript>acid</subscript> hydrogen bond that encloses an S (6) ring motif. The complex three-dimensional structure of II features N <subscript>amino</subscript> -H⋯O <subscript>acid</subscript> , N <subscript>py</subscript> -H⋯O <subscript>acid</subscript> and several C <subscript>ar</subscript> -H⋯O <subscript>acid</subscript> hydrogen bonds. In the crystal of I , the common charge-assisted 2-amino-pyridinium-carboxyl-ate heterosynthon exhibited in many 2-amino-pyridinium carboxyl-ates is not observed, instead chains of N-H⋯O hydrogen bonds and hetero O-H⋯O dimers are formed. In the crystal of II , the 2-amino-pyridinium-carboxyl-ate heterosynthon is sustained, while hetero O-H⋯O dimers are not observed. The crystal structures of both salts display a variety of hydrogen bonds as almost all of the hydrogen-bond donors and acceptors present are involved in hydrogen bonding.
Details
- Language :
- English
- ISSN :
- 2056-9890
- Volume :
- 74
- Issue :
- Pt 8
- Database :
- MEDLINE
- Journal :
- Acta crystallographica. Section E, Crystallographic communications
- Publication Type :
- Academic Journal
- Accession number :
- 30116573
- Full Text :
- https://doi.org/10.1107/S2056989018009787