Abstract
The compound [Cu2(bipym)3(sac)2(H2O)2](sac)2(H2O)4 (bipym = 2,2′-bipyrimidine and sac = saccharin) crystallizes in the space group P-1, with a = 10.710(3), b = 10.725(3), c = 13.637(5) Å, a = 70.07(3), β = 80.31(2), g = 82.87(3)° and Z = 2. The geometry in the centrosymmetric dinuclear complex around each CuII ion is a distorted octahedron, in which the equatorial plane is formed by a nitrogen atom of a bis-didentate bridging bipym ligand, two nitrogen atoms of a didentate bipym ligand, and the nitrogen atom of a coordinating sac ligand. The axial positions in the octahedron are occupied by a second nitrogen of the bis-didentate bridging bipym ligand and a water molecule. The lattice contains two saccharinate anions and four water molecules held together in a hydrogen-bonded network. The i.r vibrations of the bipym ligand are found as a quasi-symmetric doublet at 1558 and 1580 cm−1, while the most important i.r vibrations of the sac ligand are observed at 1629 and 1644 cm−1 (carbonyl vibrations) and at 1285 and 1159 cm−1 (sulfonyl vibrations). The magnetic exchange interactions between the Cu ions is very weak and is ferromagnetic (J < 0.1 cm−1).
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van Albada, G.A., Riggio, I., Reedijk, J. et al. Synthesis, spectroscopy, magnetism and X-ray structure of μ-(bipyrimidine)-bis[aqua(bipyrimidine)(saccharinato)copper(II)] bis(saccharinate) tetrahydrate. Transition Metal Chemistry 27, 341–345 (2002). https://doi.org/10.1023/A:1014859027679
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DOI: https://doi.org/10.1023/A:1014859027679