Abstract
Abstract Mixed ligand metal(II) complexes of the type [ML{XC(COCH3)2} (H2O)n] [M = Cu(II), Ni(II) and Zn(II); L = 2-formyl-, 2-acetyl- or 2-benzoyl- cyclohexanone; X = H, Cl, Br, CONHPh; n = 0,1,2] have been prepared and characterized by elemental analyses, magnetic measurements, infrared, 1H NMR, EPR and electronic spectral studies. The halogenation of the parent complexes with N-bromosuccinimide and N-chlorosuccinimide caused substitution at the τ -positionintheacetylacetonering. Reactionsofthe complexes with phenylisocyanate produced monoamides. The UV and IR spectra of the products and the 1H NMR spectra of the complexes are all consistent with τ-substitution. The copper(II) complexes are anhydrous and square-planar whereas thedihydratednickel(II)complexesareoctahedral. Zinc (II) complexes are monohydrated. In the mixed ligand complexes ν(C=O). is sensitive to the metal coordinated to it in contrast to that observed in bisacetylacetonates. EPRspectralstudiesofcopper(II)complexesindicatethat they are square-planar with dx2-y2 ground state. MO coefficientsderived from EPR parametersshowthat the mixed ligand complexes are more covalent then the corresponding bis-chesates.
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More From: Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry
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