Crystal structure and Hirshfeld surface analysis of 2-{[2,8-bis(trifluoromethyl)quinolin-4-yl](hydroxy)methyl}piperidin-1-ium 2-hydroxy-2-phenylacetate hemihydrate

Wardell, James L. and Jotani, Mukesh M. and Tiekink, Edward R. T. * (2016) Crystal structure and Hirshfeld surface analysis of 2-{[2,8-bis(trifluoromethyl)quinolin-4-yl](hydroxy)methyl}piperidin-1-ium 2-hydroxy-2-phenylacetate hemihydrate. Acta Crystallographica Section E Crystallographic Communications, 72 (11). pp. 1618-1627. ISSN 2056-9890

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Abstract

The asymmetric unit of the title salt, C17H17F6N2O+·C8H7O3-·0.5H2O, comprises a pair of pseudo-enanti­omeric (i.e. related by a non-crystallographic centre of symmetry) piperidin-1-ium cations, two carboxyl­ate anions and a water mol­ecule of crystallization. The cations have similar conformations approximating to a letter, L: one of them shows disorder of its -CF3 group over two sets of sites in a 0.775 (3):0.225 (3) ratio. Distinctive conformations are found for the anions, one with the carboxyl­ate group lying to one side of the plane through the phenyl ring and the other where the oxygen atoms lie to either side of the plane. In the latter, an intra­molecular hy­droxy-O-H...O(carboxyl­ate) charge-assisted hydrogen bond is found. The packing features extensive O-H...O,N hydrogen bonding, often charge-assisted; C-H...[pi] inter­actions are also formed. The hydrogen bonding results in the formation of five distinctive supra­molecular synthons and assembles mol­ecules in the ac plane. The quinolinyl rings lie to either side of the layer and inter-digitate with layers on either side, are approximately parallel to the b axis and are connected by [pi]-[pi] [inter-centroid separation = 3.6904 (18) Å] as well as C-F...[pi](quinolin­yl) inter­actions to consolidate the three-dimensional crystal. The dominance of the conventional hydrogen bonding in the mol­ecular packing is confirmed by an analysis of the Hirshfeld surface.

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