Abstract
Complexes [Zn(C6H5CONH2)2Br2] and [Zn((NH2)2CO)2Br2] were synthesized and characterized by elemental analysis, IR spectroscopy, and X-ray diffraction and compared to other complexes of zinc halides with benzamide and urea. In all complexes, the zinc ion has a tetrahedral coordination environment of two halide ligands and two oxygen atoms of two amide ligands. The structure of [Zn(C6H5CONH2)2Br2] (orthorhombic, Pna21, a = 29.207(6), b = 7.5826(14), c = 14.753(3) Å, Z = 8) is not isostructural to the chloride and iodide compounds. The [Zn((NH2)2CO)2Br2] complex (triclinic, P-1, a = 6.4435(9), b = 7.096(1), c = 11.7079(18) Å, α = 88.119(9)°, β = 77.005(9)°, γ = 66.320(8)°, Z = 2) is isostructural to [Zn((NH2)2CO)2Cl2], and they both differ from [Zn((NH2)2CO)2I2]. Dipole moments of complexes of various zinc halides with benzamide, urea, and dimethylformamide were calculated; they vary in the 9–13 D range. Complexes of zinc halides with amides were used to prepare films with the use of cellulose diacetate as a polymer matrix. Dielectric measurements showed the presence of a pronounced electret effect.
Graphical Abstract
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Acknowledgements
Instrumental chemical analysis was performed in the Center for Collective Use (Instrumental chemical analysis and complex research of substances and materials) at the Lomonosov Institute of Fine Chemical Technologies, RTU MIREA. The XRD experiments were carried out at the Center for Collective Use of Physical Methods of Investigation of the Frumkin Institute of Physical Chemistry and Electrochemistry of the Russian Academy of Sciences. Electret films were prepared and studied in the Ivanovo State University of Chemistry and Technology.