A rapid and sensitive spectrophotometric method is described for the determination of trace amounts of selenium using Variamine Blue (VB) as a chromogenic reagent. The proposed method is based on the reaction of selenium with potassium iodide in an acidic medium to liberate iodine, which oxidizes Variamine Blue to form a violet-colored species having an absorption maximum at 546 nm. Beer's law is obeyed in the range 2-20 g of selenium in a final volume of 10 ml. The molar absorptivity and Sandell's sensitivity were found to be 2.6 x 10(4) l mol-1 cm-1 and 0.003 microgram cm-2, respectively. The optimum reaction conditions and other analytical parameters were evaluated. The effect of interfering ions on the determination is described. The proposed method has been successfully applied to the determination of selenium in real samples of water, soil, plant materials, human hair, and synthetic samples of cosmetics and pharmaceutical preparations.

A detailed investigation of photocatalytic degradation of Acid Yellow 36 (AY36) has been carried out in aqueous heterogeneous medium containing ZnO as photocatalyst in a batch reactor. The effects of some parameters such as pH, catalyst loading, and ethanol concentration were examined. Solutions with initial concentration of 50 mg L⁻¹ of dye, within the range of typical concentration in textile wastewaters, were treated at natural pH of 6.93 and catalyst concentration of 1 g L⁻¹ after 180 min irradiation. Investigations on the active species indicated that hydroxyl radicals play the major role in the process. Experiments showed that the most efficient pH on the removal of the dye with photocatalytic degradation process was 8; however, acidic pH was favored for the dark surface adsorption. Electrical energy consumption per order of magnitude for photocatalytic degradation of AY36 has been also determined.

A bidentate (N- and O-) imine-based ligand (L₁) and its metal complexes of types [CuII(L₁)₂] (C₁), [CuII(L₁)(Phen)] (C₂), [CoIII(L₁)₂] (C₃), and [CoIII(L₁)(Phen)] (C₄) (L₁ = 2-((E)-(6-fluorobenzo[d]thiazol-2-ylimino)methyl)-4-chlorophenol and phen = 1,10-phenanthroline) were synthesized as potential chemotherapeutic drug candidates. The prepared complexes were structurally characterized by spectral techniques (NMR, FT-IR, LC-MS, EPR, and electronic absorption), thermogravimetric analysis (TGA/DTA), magnetic moment, and CHNO elemental analysis. Spectroscopic studies suggested the distorted octahedral structure for all complexes. In vitro bioassay studies include binding and nuclease activities of the ligand and its complexes with target calf thymus- (CT-) DNA were carried out by employing UV-Vis, fluorescence spectroscopy, viscosity, and gel electrophoresis techniques. The extent of binding propensity was determined quantitatively by Kb and Ksv values which revealed a higher binding affinity for C₂ and C₄ as compared to C₁ and C₃. In addition, the scavenging superoxide anion free radical (O∙-2) activity of metal complexes was determined by nitroblue tetrazolium (NBT) light reduction assay. Molecular docking studies with DNA and SOD enzyme were also carried out on these compounds. The antimicrobial study has shown that all the compounds are potential antibacterial agents against Gram-negative bacterial strains and better antifungal agents with respect to standard drugs used.