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EPR spectra and structures of dinuclear copper(II) complexes with acyldihydrazones of benzenedicarboxylic acids

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Abstract

Spacer-armed dinuclear copper(II) complexes with condensation products of isophthalic and terephthalic acid dihydrazides with salicylaldehyde and 2-hydroxyacetophenone were synthesized and studied by EPR and X-ray diffraction. The compositions and structures of most of the complexes were determined by elemental analysis, thermogravimetric analysis, and IR spectroscopy. The structure of the copper(II) complex with acyldihydrazone of salicylaldehyde and 1,3-benzenedicarboxylic acid (H4L) with the composition [Cu2L1·2morph·MeOH] (morph is morpholine) was established by X-ray diffraction. The CuII atoms are spaced by 10.29 Å and are structurally nonequivalent. One copper cation has a square-planar coordination formed by donor atoms (2 N + O) of the doubly deprotonated acylhydrazine fragment and the N atom of the morpholine molecule. The second copper atom is additionally coordinated by a methanol molecule through the oxygen atom, so that this copper atom is in a tetragonal-pyramidal coordination with the oxygen atom in the axial position. The EPR spectra of liquid solutions of the complexes based on 1,4-benzenedicarboxylic acid acyldihydrazones and 1,3-benzenedicarboxylic acid bis(salicylidene)hydrazone at room temperature show a four-line hyperfine structure with the constant a Cu = 54.4–67.0·10−4 cm−1 (g = 2.105–2.147), which is indicative of the independent behavior of the paramagnetic centers. The EPR spectrum of a solution of the complex based on isophthalic acid and 2-hydroxyacetophenone shows the seven-line hyperfine structure corresponding to two equivalent copper nuclei (g = 2.11, a Cu = 36.5·10−4 cm−1).

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Correspondence to G. M. Larin.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1898–1905, October, 2007.

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Larin, G.M., Gusev, A.N., Trush, Y.V. et al. EPR spectra and structures of dinuclear copper(II) complexes with acyldihydrazones of benzenedicarboxylic acids. Russ Chem Bull 56, 1964–1971 (2007). https://doi.org/10.1007/s11172-007-0306-7

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  • DOI: https://doi.org/10.1007/s11172-007-0306-7

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