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Abstract
When a mixture of excess CuSCN and 2-benzoylpyridine (2-Bzpy) stands in an ethanolic medium for about ten days in contact with air, the intramolecular oxidative cyclization of 2-Bzpy occurs with formation of the ionic compound [9-oxo-indolo[1,2-a]pyridinium]+ [Cu(SCN)2]− (1). In contrast, interaction of CuCN and 2-Bzpy in ethanol leads to formation of the polymer [Cu(CN)(2-Bzpy)]n (2). The reaction of Cu(II) and 2-Bzpy in presence of excess SCN− in ethanol affords (1) and the green monomer [Cu(SCN)2(2-Bzpy)2] (4). These complexes, along with the 1:1 CuSCN complex of 2-Bzpy (3) are studied by IR, Raman and electronic spectroscopic methods and X-ray structural analysis of (1) and (2). Crystals of (1) are monoclinic, space group P21/n (No. 14), with a = 5.887(1), b = 36.142(7), c = 7.083(1) Å, B = 109.56(1)°, Z = 4, and RF = 0.033 for 2487 observed MoKα data, (2) monoclinic, space group P21/c (No. 14), a = 14.393(3), b = 8.881(2), c = 9.287(2) Å, B = 103.80(3)°, Z = 4, and RF = 0.036 for 2030 observed MoKα data. The structure of (1) consists of a packing of [9-oxo-indolo [1,2-a]pyridinium]+ cations and [Cu(SCN)2]− anions. Puckered layers are formed by the [Cu(SCN)2]− component with four-coordinate Cu(I) and one tridentate μ(N,S,S)-thiocyanato ligand. Complex (2) features distorted tetrahedral Cu(I) geometry, formed by a bidentate chelating 2-Bzpy and linear C- and N-bonded bidentate cyano groups, which link adjacent copper centers to form zigzag chains extending along the c axis. Complexes (1) and (2) do not fluoresce at room temperature.
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