Synthesis and spectroscopic studies of new binuclear transition metal complexes of Schiff bases derived from 4,6-diacetylresorcinol

• Published in: Transition metal chemistry (Weinheim) Vol. 32; no. 7; pp. 889 - 901
• Main Authors: Emara, Adel A. A., Adly, Omima M. I.
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Nature B.V 01.10.2007
• ISSN: 0340-4285; 1572-901X
• DOI: 10.1007/s11243-007-0245-z

Two new series of copper(II), nickel(II), cobalt(II), zinc(II), iron(III), chromium(III), vanadyl(IV) and uranyl(VI) complexes with two bifunctional tridentate Schiff base, H^sub 4^L^sup 1^ and H^sub 2^L^sup 2^ ligands have been prepared. The Schiff base, H^sub 4^L^sup 1^ and H^sub 2^L^sup 2^, ligands were synthesized by the condensation of 4,6-diacetylresorcinol with o-aminophenol or o-phenylenediamine. The ligands are either di- or tetra-basic with two symmetrical sets of either OON or NNO tridentate chelating sites. The ligands and their metal complexes have been characterized by elemental analysis, ^sup 1^H-n.m.r., FT-IR, mass, electronic, esr spectra and thermal gravimetric analysis and magnetic susceptibility. With the exception of Co^sup II^ ion with H^sub 2^L^sup 2^ which afforded a trinuclear complex, a variety of binuclear complexes for the rest of the metal complexes were obtained with the ligands in its di- or tetra-deprotonated forms. The bonding sites are the azomethine and amino nitrogen atoms, and phenolic oxygen atoms. The metal complexes exhibit different geometrical arrangements such as square planar, tetrahedral, square pyramid and octahedral arrangement.[PUBLICATION ABSTRACT]