In the title compound, [Cu(C2O4)(C13H20N4)(H2O)]·2H2O, the CuII atom exhibits a distorted square-pyramidal geometry with the two N atoms of the imidazole ligand and the two O atoms of the oxalate ligand forming the basal plane, while the O atom of the coordinated water molecule is in an apical position. The CuII atom is shifted 0.232 (2) Å out of the basal plane toward the water molecule. The asymmetric unit is completed by two solvent water molecules. These water molecules participate in the formation of an intricate three-dimensionnal network of hydrogen bonds involving the coordinated water molecule and the NH groups.
Key indicators: single-crystal X-ray study; T = 298 K; mean (C-C) = 0.005 Å; disorder in main residue; R factor = 0.040; wR factor = 0.114; data-to-parameter ratio = 14.7.In the title compound, [CoCl 2 (C 13 H 20 N 4 )]ÁH 2 O, the Co II atom lies on a mirror plane and is four-coordinated by two N atoms of the imidazole ligand and two Cl atoms in a distorted tetrahedral arrangement. The water molecule participates in the formation of hydrogen bonds, resulting in a three dimensional network involving the Cl atoms and the NH groups. The terminal C atom of the ethyl group is disordered over two sites of equal occupancy.
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In the title compound, [Ni(NO3)(C13H20N4)2]NO3, the NiII ion shows a distorted octahedral geometry formed by four N atoms from two bis(2-ethyl-5-methyl-1H-imidazol-4-yl)methane ligands and two O atoms from a chelating nitrate anion. Three ethyl groups in the complex cation and the O atoms of the uncoordinated nitrate anion are disordered over two sets of positions [occupancy ratios of 0.52 (3):0.48 (3) and 0.63 (3):0.37 (3), respectively]. In the crystal, intermolecular N—H⋯O hydrogen bonds connect the complex cations into a zigzag chain along [010] and further N—H⋯O hydrogen bonds between the chains and the uncoordinated nitrate anions lead to layers parallel to (100).
The crystal structure of the title compound, C6H7NO, is stabilized by intermolecular N—H⋯O hydrogen bonds, resulting in inversion dimers. The structure is further consolidated by weak C—H⋯O hydrogen bonds.
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