ascorbic-acid has been researched along with salicylaldehyde* in 2 studies
2 other study(ies) available for ascorbic-acid and salicylaldehyde
Article | Year |
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A novel dinuclear Schiff-base copper(II) complex modified electrode for ascorbic acid catalytic oxidation and determination.
A new dinuclear copper salicylaldehyde-glycine Schiff-base complex [Cu(2)(Sal-Gly)(2)(H(2)O)(2)] was synthesized and structurally characterized. [Cu(2)(Sal-Gly)(2)(H(2)O)(2)] crystallized in the monoclinic system in the P2(1)/c space group. The molecule is a dinuclear complex, formed by two [Cu(Sal-Gly)(H(2)O)] units. The electropolymerization properties of the copper complex on a glass carbon electrode were studied at different potential ranges. The electropolymerization occurred when the high scan potential reached 1.4 V. The modified electrode exhibited good electrocatalytic oxidation properties to ascorbic acid and showed a sensitivity of 22.9 nA μM(-1) (r(2) = 0.9998) and detection limit of 0.39 μM (S/N = 3) in the amperometric determination of ascorbic acid. The designed determination method can be used to analyze vitamin C tablets. Topics: Aldehydes; Ascorbic Acid; Carbon; Catalysis; Copper; Electrochemistry; Electrodes; Glycine; Models, Molecular; Molecular Conformation; Organometallic Compounds; Oxidation-Reduction; Polymerization; Schiff Bases | 2012 |
DNA binding and nucleolytic properties of Cu(ii) complexes of salicylaldehyde semicarbazones.
The copper(ii) complexes of two salicylaldehyde semicarbazones, HOC(6)H(4)CH[double bond, length as m-dash]N-NHCONR(2) [H(2)Bnz(2) (R = CH(2)Ph) and H(2)Bu(2) (R = Bu)], were evaluated for their DNA binding and cleavage properties by spectrophotometric DNA titration, ethidium bromide displacement assay and electrophoretic mobility shift assay. Results showed that the Cu(ii) complexes can bind to DNA via a partial intercalation mode with binding constants of 1.1 × 10(4) and 9.5 × 10(3) M(-1) for [Cu(HBnz(2))Cl] and [Cu(HBu(2))Cl], respectively. These complexes also cleave DNA in the presence of ascorbic acid, most likely through hydroxyl radicals that are generated via the reduction of a Cu(ii) to a Cu(i) species. The complexes show similar DNA cleavage activity, which is reflected in the similarity of their frontier molecular orbital energies calculated by density functional theory. These results are discussed in relation to the anticancer properties of the complexes. Topics: Aldehydes; Ascorbic Acid; Cations, Divalent; Coordination Complexes; Copper; Deoxyribonucleases; DNA; DNA Cleavage; DNA, Superhelical; Ethidium; Models, Molecular; Plasmids; Semicarbazones; Spectrometry, Fluorescence | 2012 |