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A new polymorph of a mononuclear nickel(II) acetate com­plex with 2-(pyridin-2-yl)ethanol ligands, [Ni(CH3COO)2(C7H9NO)2], has been prepared and structurally characterized. Its mol­ecular structure resembles the structures of two previously reported polymorphs in that the NiII atom is located on an inversion centre and is coordinated by pairs of acetate and 2-(pyridin-2-yl)ethanol ligands. The acetate anions are coordinated in a monodentate manner, while the 2-(pyridin-2-yl)ethanol ligands are coordinated in a bidentate chelating mode involving the endocyclic N atom and the hy­droxy O atom of the ligand side chain. A strong bifurcated intra­molecular hydrogen-bond inter­action was observed involving the hy­droxy O atom as donor and both acetate O atoms as acceptors. No classical inter­molecular hydrogen-bond contacts were observed. However, the crystal packing is effected through π–π and C—H...π inter­actions, giving rise to a different packing arrangement. A brief comparison of the three polymorphic forms is presented.
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