Synthesis, characterisation and antifungal activity of a series of Cobalt(II) and Nickel(II) complexes with ligands derived from reduced N, N′-o-Phenylenebis(Salicylideneimine)

The synthesis and characterisation by elemental analysis, conductivity, FTIR, UV–Visible, ESR and magnetic measurements are described for a series of complexes of nickel(II) and cobalt(II) with three ligands (H2L1–3) derived from reduced N, N′-o-Phenylenebis(salicylideneimine). The complexes formed are identified as neutral species, where the ligands are coordinated through N and O donor atoms. The formulae obtained for the complexes are: [CoL(H2O)2] with octahedral geometry and [NiL] with tetrahedral geometry. Their antifungal activity is evaluated towards human pathogenic fungi including yeasts of the Candida genus, some opportunistic moulds belonging to the Aspergillus, Scedosporium genus and some dermatophytes. The cobalt complexes show a significant growth inhibition of yeasts tested and also to fungi of the genus Scedosporium which is of interest because these fungi are usually poorly susceptible to current antifungal including Amphotericin B and Itraconazole, chosen as reference in this study. The activity data show that the metal complexes are more potent than the parent ligand

Synthesis, characterization and antifungal activity of a series of manganese(II) and copper(II) complexes with ligands derived from reduced N,N′-O-phenylenebis(salicylideneimine)

A series of manganese(II) and copper(II) complexes with reduced Schiff bases derived from o-phenylenediamine has been prepared and characterized by elemental analysis, TG measurements, ESR, magnetic measurements, FTIR, UV–Visible spectra and conductivity. These complexes were found to be [MnL(H2O)n] and [CuL](H2O)n species with n = 0–2. Their antifungal activity was evaluated on different human fungi including yeasts of the Candida genus (C. albicans, C. glabrata, C. tropicalis and C. parapsilopsis) some opportunistic moulds belonging to the Aspergillus (A. fumigatus, A. terreus and A. flavus), Scedosporium genus (S. apiospermum and S. prolificans) and some dermatophytes (M. gypseum, M. persicolor, T. mentagrophytes, M. canis and T. tonsurans). The manganese complexes showed a significant growth inhibition of the dermatophytes tested and fungi of the genus Scedosporium. This is very interesting as these fungi are usually poorly susceptible to current antifungal including Amphotericin B and Itraconazole chosen as reference in this study

Spectrometric Analyses, Structure and Voltammetric Study of Nickel(II) with N[(1E) Phenylmethylene N2[2(2Hydroxyphenylmethylene]Amino ethyl) Imidazolidin-1-yl Ethylamine

The reaction of N[(1E) phenylmethylene N2[2(2hydroxyphenylmethylene]amino ethyl) imidazolidin -1-yl ethylamine ligand (H 3 L) with nickel(II) salt, by heating at 40°C and addition of NaOH in excess, was made by eliminating of the phenol substituted imidazolidine ring, giving the mononuclear nickel(II) complex of the deprotonated bis-salicylaldehyde-triethylenetetramine (L −2 ). UV-Vis, FTIR and structural resolution show an octahedral geometry for [NiL]·6H 2 O complex. This compound has been characterized by single crystal X-ray diffraction study. This technique reveals that Ni-H 2 L involves a high-spin nickel(II) ion within a pseudo-octahedral geometry. The Ni(II) complex has NiN 4 O 2 coordination sphere as established from a crystal structure determination. The crystals of Ni(II) complex are tetragonal, space group P4/ncc, a = b = 19.348 A; c = 13.201 A. R(F) value (0.0528) found shows a very good precision of the determined geometrical parameters. Cyclic voltammetry of nickel complex is indicative of electronic communication between the nickel center via Schiff base ligand. The results obtained confirm the imidazolidine ring-cleavage reaction and the elimination of the substituted phenol on this ring and show that the presence of H 3 L ligand around the metallic center stabilizes the oxidation of the Ni(II) to Ni(III)