As a result of [1+2] Schiff base condensation in the template reaction between 2,6-diacetylpyridine and 3,7-diazanonane-1,9-diamine in the presence of rare earth(III) ions (M = Y3+, La3+, Pr3+, Sm3+, Eu3+, Gd3+, Tb3+, Ho3+, Er3+, Tm3+, Yb3+), new dinuclear architectures containing a ligand with N9 set of donor atoms with terminal amine groups have been formed. The complexes have been characterized by the spectroscopic and thermogravimetric data and microanalyses.
Homodinuclear complexes with magnesium(II), calcium(II), and barium(II) ions and heterodinuclear complexes with calcium(II) or cadmium(II) and lanthanide(III) ions containing Schiff base open-chain ligand terminated by one amine and one carbonyl group were prepared as a result of the partial Schiff base condensation reaction between 2,6-diacetylpyridine and 4-methyl-1,2-phenylenediamine in the presence of the appropriate ions acting as templates. The complexes were characterized by spectroscopic methods (IR, 1H NMR, FAB-MS), thermogravimetric and elemental analyses.
Homodinuclear complexes of lanthanum(III), zinc(II), cadmium(II) and mercury(II) ions and heterodinuclear complexes of lanthanum(II) and zinc(II) ions containing Schiff base open-chain ligands terminated by two carbonyl groups or one amine and one carbonyl group were prepared as a result of the partial Schiff base condensation reaction between 2,6-diacetylpyridine and 4-methyl-1,2-phenylenediamine or 2,6-diaminopyridine in the presence of the appropriate ions acting as templates. The complexes were characterized by spectroscopic methods (IR, 1H NMR, FAB-MS) and elemental analysis.
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