Abstract

The complex of cobalt(II) chloride with bi-1,1′-(3,3-dimethyl-3,4-dihydroisoquinoline) (L), [CoLCl2] (I), is synthesized and studied by X-ray diffraction, electronic spectroscopy, and IR spectroscopy. In the structure of complex I, ligand L performs a bidentate-chelating function, adding to the cobalt atom through the nitrogen atoms. The coordination polyhedron of the cobalt atom is a tetrahedron (2N, 2Cl) with ordinary Co-N (2.00(1)–2.07(1) A) and Co-Cl (2.216(6)–2.226(6) A) bond lengths. The noncentrosymmetric orthorhombic unit cell of crystal I contains two independent molecules of the complex (1 and 1′) joined by C-H=Cl hydrogen bonds into a pseudocentrosymmetric dimer. Ligands Lc and Lc′ exist in the same cisoid isomeric form (torsion angle N(1)-C(1)-C(12)-N(2) is 19.2° in Lc and 26.6° in Lc′).

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