211 research outputs found
Synthesis and Properties of Complexes of Copper(II), Nickel(II), Cobalt(II) and Uranyl Ions with 3-(p-Tolylsulphonamido)rhodanine
Metal complexes of copper(II), nickel(II), cobalt(II), uranyl(II) with 3-(p-tolylsulphonamido)rhodanine (HL) have been prepared and characterized by chemical and thermal analyses, molar conductivity, magnetic susceptibility measurements, and infrared, electronic and EPR spectra. The visible and EPR spectra indicated that the Cu(II) complex has a tetragonal geometry. From EPR spectrum of the Cu(II) complex, various parameters were calculated. The crystal field parameters of Ni(II) complex were calculated and were found to agree fairly well with the values reported for known square pyramidal complexes. The infrared spectral studies showed a monobasic bidentate behaviour with the oxygen and nitrogen donor system. Thermal stabilities of the complexes are also reported
Metal Complexes of Multidentate N2S2 Heterocyclic Schiff-base Ligands;Formation, Structural Characterisation and Biological Activity
The synthesis of ligands with N2S2 donor sets that include imine, an amide, thioether, thiolate moieties and their metal complexes were achieved. The new Schiff-base ligands; N-(2-((2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9-ylidene)amino)ethyl)-2-((2-mercaptoethyl)thio)-acetamide (H2L1) and N-(2-((2,4-di-p-tolyl-3-azabicyclo[3.3.1]nonan-9-ylidene)amino)ethyl)-2-((2-mercaptoethyl)thio) acetamide (H2L2) were obtained from the reaction of amine precursors with 1,4-dithian-2-one in the presence of triethylamine as a base in the CHCl3 medium. Complexes of the general formula K2[M(Ln)Cl2], (where: M = Mn (II), Co(II) and Ni(II)) and [M(Ln)], (where: M = Cu(II), Zn(II) and Cd(II); n =1-2, expect [Cu(HL2)Cl]) were isolated. The entity of ligands and complexes including their purity were confirmed using elemental microanalysis (C.H.N.S), atomic absorption (A.A), chloride content, conductivity measurement's, melting point and thermal analysis technique. The molecular structures were elucidated with FT-IR, UV-Vis, magnetic susceptibility, 1H-and 13C-NMR and mass spectroscopy. The synthesised compounds were evaluated for their activity against bacterial strains (G+ and G-) and fungi species. The tested compounds indicated that; the ligands have not shown any antimicrobial activity against Escherichia coli. The Cd(II) complexes, for ligands H2L1 and H2L2, display the higher antimicrobial activity, compared with the other complexes. The H2L1 and H2L2 have not shown any activity against Candida albicans. All complexes for ligands (H2L1 and H2L2) exhibited less activity against Candida albicans, compared with other types of fungi
Optical, morphological and photocatalytic properties of biobased tractable films of chitosan/donor-acceptor polymer blends
Biobased tractable films consisting of blends of chitosan (CS) with polymer bearing carbazole derivatives as
pendant groups and fluorene-thiophene as donor-acceptor units (referred to as DA) were prepared, and their
optical, morphological and photocatalytic properties were studied. DA was dissolved in tetrahydrofuran (THF)
and mixed with an acidified aqueous solution containing chitosan to obtain chitosan/DA (CS/DA) films by
solution casting. The fabricated biobased films were characterized using spectroscopic techniques (FT-IR and
UV–vis), thermogravimetry, mechanical assays, contact angle analysis, and atomic force microscopy (AFM). The
effects of varying DA compositions and the results of exposure to visible-light irradiation of the films were also
analyzed. The results indicated the existence of interactions between chitosan and DA and a potentially profitable
light-driven response of these biobased films. This behavior was reflected in the optical, topographical,
and contact angle properties of the films, which exhibited different characteristics before and after visible-light
exposure. Finally, the photocatalytic performance of the biobased films was tested via the decomposition of
methyl orange (MO), as a reaction model system. Our results revealed a significant photocatalytic activity
(according to biobased film composition, approximately 64 % and 87 % of methyl orange were degraded under
continuous visible-light irradiation for 120 min) of the films which is attributed to the combined presence and
synergetic effects of the film-forming ability of chitosan and the photoproperties of DA
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