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Surface introduction of an amorphous borate shell on NiCo<sub>2</sub>O<sub>4</sub> greatly boosts its electrochemical water oxidation activity under alkaline conditions. To achieve 10 mA cm<sup>−2</sup> in 1.0 M KOH, NiCo<sub>2</sub>O<sub>4</sub>@Ni–Co–B/CC needs an overpotential of only 270 mV.
Se doped Fe<sub>2</sub>O<sub>3</sub> nanorod arrays (Se-Fe<sub>2</sub>O<sub>3</sub>) show superior solar water oxidation activity driving 1.44 mA cm<sup>−2</sup> at 1.23 V <italic>vs.</italic> the RHE in 1.0 M NaOH under simulated light irradiation, 3.13 times that of pure Fe<sub>2</sub>O<sub>3</sub>, with a 90 mV cathodic shift of onset potential.
For the first time we demonstrate the topotactic synthesis of a three-dimensional (3D) interconnected network of nanoporous CoP nanowires directly on a Ti substrate (np-CoP NWs/Ti) via low-temperature phosphidation of a Co2(OH)2(CO3)2/Ti precursor and its further use as a highly efficient hydrogen evolution cathode.
The exocyclic C=C double-bond in the title compound, C(11)H(12)OS, has an E configuration. The methyl-bearing C atom in the cyclo-pentane ring is disordered over two positions with a site-occupation factor of 0.899 (8) for the major occupied site.
The nine-membered fused-ring system of the title pyridazine derivative, C(7)H(7)N(3)OS, is almost planar (r.m.s. deviation 0.012 Å). In the crystal, the amino H atom forms a hydrogen bond to the ketonic O atom of a neighboring mol-ecule to generate a centrosymmetric dimer.
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 simple and sensitive spectrophotometric method has been proposed for the determination of flutamide (FLD). The method is based on its complexation and oxidation of FLD by Fe3+ and 1,10-phenanthroline. Two sets of condition were established. In the first set only FLD reacted with Fe3+ ion, while in the second one FLD was oxidized by Fe3+ in the presence of 1,10-phenanthroline. The complexation and oxidation methods were monitored spectrophotometrically. All variables affecting the development of the color were investigated and the conditions obeying Beer’s law were optimized. Plots of absorbance against concentration in both methods were rectilinear over the ranges 0.5–10 and 0.5–1.5 μg mL−1, with mean recoveries of 99.51 and 99.83 for methods A and B respectively. The limits of detection for procedures 1 and 2 are 0.332 and 0.726 μg mL−1 1, respectively. Both the methods were successfully applied for the determination of the FLD in its dosage form.