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Co<sub>3</sub>O<sub>4</sub> nanosheets were synthesized by wet chemical technique at low-temperature in alkaline phase.
Iron oxide nanoparticles (NPs) was prepared sono-chemically in presence of ultrasonic irradiation in aqueous alkaline medium at room conditions, where ferric chloride and urea were used as starting materials. NPs were characterized using powder X-ray diffraction, field-emission scanning electron microscopy, UV/vis. X-ray photoelectron, Fourier-transform infra-red spectroscopy (FT-IR), and Raman spectroscopy, etc. They were deposited on a flat polycrystalline gold electrode (AuE, surface area, 0.0216 cm2) to give a sensor with a fast response towards selective ion (i.e., fluoride ion, F−) in phosphate buffer system. The fabricated chemi-sensor also exhibits good sensitivity, lower detection limit, and long-term stability as well as enhanced electrochemical responses towards the target analyte. The calibration plot is linear (r2: 0.9598) over the 0.1 nM to 1.0 mM fluoride concentration ranges. The sensitivity and detection limit is ∼1.8718 μA cm−2 mM−1 and ∼0.092 ± 0.02 nM (at a Signal-to-Noise-Ratio of 3) respectively in short response time (10.0 s). Finally it was confirmed that the nanostructures and the optical features of iron oxide can be extended to a large range in un-doped semiconductor nanomaterials for proficient chemical sensor applications.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
A series of 1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one-containing Schiff bases were synthesized, characterized and screened for their antibacterial activities. The structures of the synthesized compounds were established by spectroscopic (FT-IR, ¹H-NMR, ¹³C-NMR, MS) and elemental analyses. The anti-bacterial activities (with MIC values) of compounds were evaluated. The anti-bacterial screening results reveal that among the six compounds screened, four compounds showed moderate to good anti-bacterial activity. Among the tested compounds, the most effective compounds against four bacterial strains, viz. Escherichia coli, Staphylococcus aureus, Salmonella typhimurium and Streptococcus pyogenes, are [(2-chlorobenzylidene)amino]-1,5-dimethyl-2-phenyl-1,2-dihydropyrazol-3-one (4) and [(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-ylimino)methyl]benzonitrile (5) with MIC values of 6.25 μg/mL.
Electrochemical reduction has been regarded as a sustainable strategy to tackle energy-intensive operations by the Haber-Bosch process achieving catalytic conversion of N<sub>2</sub> to NH<sub>3</sub> under mild conditions. However, the challenge of N<sub>2</sub> electroconversion emphasizes the requirement of efficient electrocatalysts. In this paper, we report the development of porous bromide-derived Ag film (BD-Ag/AF) as an efficient electrocatalyst for N<sub>2</sub> reduction reaction. During electrochemical test, Br<sup>-</sup> anions are released and adsorbed onto the surfaces of the electrode, suppressing hydrogen evolution reaction. Such BD-Ag/AF shows a high Faradaic efficiency of 7.36% at -0.6 V vs reversible hydrogen electrode in 0.1 M Na<sub>2</sub>SO<sub>4</sub>, which is higher than that (0.38%) of porous Ag film without Br<sup>-</sup> anions. Moreover, it exhibits excellent long-term electrochemical durability.
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The title compound, 1-{[(3,4-dimethylisoxazol-5-yl)imino]methyl}-2-naphthol has been synthesized by condensation of 5-amino-3,4-dimethylisoxazole and 2-hydroxy-1-naphthaledhyde in ethanol. The structure of this new compound was confirmed by elemental analysis, IR, 1H-NMR, 13C-NMR and EI-MS spectral analysis.