2-{[2,8-Bis(trifluoromethyl)quinolin-4-yl](hydroxy)methyl}piperidin-1-ium trichloroacetate: Crystal structure and Hirshfeld surface analysis

Wardell, James L. and Jotani, Mukesh M. and Tiekink, Edward R. T. * (2018) 2-{[2,8-Bis(trifluoromethyl)quinolin-4-yl](hydroxy)methyl}piperidin-1-ium trichloroacetate: Crystal structure and Hirshfeld surface analysis. Acta Crystallographica Section E Crystallographic Communications, 74 (12). pp. 1851-1856. ISSN 2056-9890

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Official URL: http://doi.org/10.1107/S2056989018016389

Abstract

The asymmetric unit of the centrosymmetric title salt, C17H17F6N2O+C2Cl3O2 , comprises a single ion-pair. The hydroxy-O and ammonium-N atoms lie to the same side of the cation, a disposition maintained by a charge-assisted ammonium-N—HO(hydroxy) hydrogen bond [the Oh—Cm—Cm–Na (h = hydroxy, m = methine, a = ammonium) torsion angle is 58.90 (19)⁰]. The piperidin-1-ium group is approximately perpendicular to the quinolinyl residue [Cq—Cm—Cm–Na (q = quinolinyl) is 178.90 (15)⁰] so that the cation, to a first approximation, has the shape of the letter L. The most prominent feature of the supramolecular association in the crystal is the formation of chains along the a-axis direction, being stabilized by charge-assisted hydrogen-bonds. Thus, ammonium-N+ —HO(carboxylate) hydrogen bonds are formed whereby two ammonium cations bridge a pair of carboxylate-O atoms, leading to eightmembered {OHNH}2 synthons. The resulting four-ion aggregates are linked into the supramolecular chain via charge-assisted hydroxyl-O—HO(carboxylate) hydrogen bonds. The connections between the chains, leading to a three-dimensional architecture, are of the type C—X, for X = Cl and F. The analysis of the calculated Hirshfeld surface points to the importance of XH contacts to the surface (X = F, 25.4% and X = Cl, 19.7%) along with a significant contribution from OH hydrogen-bonds (10.2%). Conversely, HH contacts, at 12.4%, make a relatively small contribution to the surface.

Item Type: Article
Uncontrolled Keywords: crystal structure; mefloquine; salt; hydrogen-bonding; Hirshfeld surface analysis
Subjects: Q Science > QD Chemistry
Divisions: Others > Non Sunway Academics
Sunway University > School of Science and Technology > Research Centre for Crystalline Materials
Depositing User: Dr Janaki Sinnasamy
Related URLs:
Date Deposited: 27 Nov 2018 01:43
Last Modified: 22 Apr 2019 05:48
URI: http://eprints.sunway.edu.my/id/eprint/943

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