Potassium Dodecatungsto Cobaltate Trihydrate: A New Heterogeneous Catalyst for the Synthesis of Homoallylic Alcohols and Amines

A simple and efficient procedure has been developed for one-pot synthesis of homoallylic alcohols and amines in good to excellent yields using a variety of aldehydes, amines, and allyltributylstannane in the presence of a catalytic amount of potassium dodecatungsto cobaltate trihydrate (K₅CoW₁₂O₄₀ · 3H₂O) as a heterogeneous catalyst at room temperature. The catalyst exhibited remarkable reusability.     

Acid base properties and catalytic activity of vanadium pentoxide supported on cerium oxide

The surface acidity and basicity of vanadium pentoxide supported on CeO₂ were determined using a set of Hammett indicators. The data have been correlated with the catalytic activity of these oxides towards liquid phase acylation of phenol.     

Preparation, characterization, magnetic susceptibility (Eu, Gd and Sm) and XPS studies of Ln2ZrTiO7 (Ln=La, Eu, Dy and Gd)

Bulk and nanosized pyrochlore materials Ln₂ZrTiO₇ (Ln=La, Eu, Dy, Gd and Sm) have been prepared by the sol-gel method. All the samples were characterized by powder X-ray diffraction, Raman and X-ray photoelectron spectroscopy. Magnetic susceptibility (χ) measurements of Gd₂ZrTiO₇, Sm₂ZrTiO₇ and Eu₂ZrTiO₇ were carried out by vibrating sample magnetometer in the temperature range 2-320 K. The variation of χ⁻¹ (or χ) with temperature of Gd₂ZrTiO₇, Sm₂ZrTiO₇ and Eu₂ZrTiO₇ follows the Curie law, intermediate formula and the Curie-Weiss law, respectively. From the linear portion of χT vs. T⁻¹ plot of Eu₂ZrTiO₇ from 2 to 15 K, the classical nearest neighbor exchange (J^cl) and dipolar interactions (D_nn) are obtained. The XPS of Ln₂ZrTiO₇ (Ln=La, Eu, Dy and Gd) gave characteristic peaks for Ln, Ti, Zr and O. The satellite peaks are observed only for 3d La of La₂ZrTiO₇.     

Stability of electrostatic ion cyclotron waves in a multi-ion plasma

We have studied the stability of the electrostatic ion cyclotron wave in a plasma consisting of isotropic hydrogen ions (H⁺) and temperature-anisotropic positively (O⁺) and negatively (O⁻) charged oxygen ions, with the electrons drifting parallel to the magnetic field. Analytical expressions have been derived for the frequency and growth/damping rate of ion cyclotron waves around the first harmonic of both hydrogen and oxygen ion gyrofrequencies. We find that the frequencies and growth/damping rates are dependent on the densities and temperatures of all species of ions. A detailed numerical study, for parameters relevant to comet Halley, shows that the growth rate is dependent on the magnitude of the frequency. The ion cyclotron waves are driven by the electron drift parallel to the magnetic field; the temperature anisotropy of the oxygen ions only slightly enhance the growth rates for small values of temperature anisotropies. A simple explanation, in terms of wave exponentiation times, is offered for the absence of electrostatic ion cyclotron waves in the multi-ion plasma of comet Halley.     

Ionic conduction behavior in PVC–PEG blend polymer electrolytes upon the addition of TiO2

The blend-based polymer electrolyte consisting of poly (vinyl chloride) (PVC) and poly (ethylene glycol) (PEG) as host polymers and lithium perchlorate (LiClO₄) as the complexing salt was studied. An attempt was made to investigate the effect of TiO₂ concentration in the unplasticized PVC–PEG polymer electrolyte system. The XRD and FTIR studies confirm the formation of a polymer–salt complex. The conductivity results indicate that the incorporation of ceramic filler up to a certain concentration (15 wt.%) increases the ionic conductivity and upon further addition the conductivity decreases. The maximum ionic conductivity 0.012 × 10⁻⁴ S cm⁻¹ is obtained for PVC–PEG–LiClO₄–TiO₂ (75–25–5–15) system. Thermal stability of the polymer electrolyte is ascertained from TG/DTA studies.     

SBA-16负载金属氧化物催化剂合成、表征及催化CO氧化反应活性

将V2O5, CeO2和CuO分散到提取自稻米壳的SBA-16上,考察了其催化CO氧化反应活性,并采用X射线衍射、扫描电镜、透射电镜、程序升温还原和紫外漫反射光谱对所制催化剂进行了表征。结果表明,掺杂CuO的介孔氧化硅是一种有前景的催化剂,其CO转化率可达98%以上。     

Effect of Cation/Anion Co‐doping on the Photocatalytic Performance of Na3SbO(PO4)2

Silver/copper‐nitrogen co‐doped Na₃SbO(PO₄)₂ were prepared by solid state/ion exchange methods. The materials were characterized by powder XRD, SEM‐EDS, TG analysis, as well as FT‐IR and UV/Vis diffuse reflectance spectroscopy. All the doped materials crystallize in orthorhombic lattice with space group P2₁2₁2₁. The infrared spectra of the samples gave characteristic bands corresponding to PO₄ and SbO₆ groups. The bandgap energy of all the samples was deduced from their UV/Vis DRS profiles. The bandgap energy of doped materials decreased substantially. Visible‐light‐induced photocatalytic oxidation of the methyl violet (MV) and methylene blue (MB) was examined. The influence of cation, anion, and co‐doping on the photoactivity of Na₃SbO(PO₄)₂ was studied. The Ag⁺ and nitrogen co‐doped Na₃SbO(PO₄)₂ exhibited the highest photocatalytic activity among the materials investigated.     

A polymer-anchored cobalt(II) complex as a reusable catalyst for oxidation of benzene,ethylbenzene and cyclohexane

A polymer-supported cobalt complex of 2,6-bis(benzimidazolyl)pyridine (BBP) was synthesized by immobilization of BBP on chloromethylated polystyrene cross-linked with 6.5 % divinylbenzene, followed by complexation with CoCl₂ in methanol, and characterized by physico-chemical and spectroscopic methods. The polymer-bound Co(PS–BBP)Cl₂ was found to be more stable compared to free Co(BBP)Cl₂ as determined by TGA analyses. The catalytic activity of Co(PS–BBP)Cl₂ was investigated towards oxidation of benzene, ethylbenzene and cyclohexane using tert-butylhydroperoxide as oxidant. At optimum conditions, benzene showed 72.6 % conversion with 100 % selectivity towards phenol; ethylbenzene exhibited 97.0 % conversion with 82.5 and 17.4 % selectivity towards benzaldehyde and acetophenone, respectively, whilst conversion of cyclohexane was 60.0 with 75.8 and 24.1 % selectivity towards cyclohexanol and cyclohexanone. The unsupported complex Co(BBP)Cl₂ showed lower activities and selectivities compared to the polymer-supported complex. Co(PS–BBP)Cl₂ was found to be very active and reusable, giving high yields of the desired products. A possible reaction mechanism is proposed for these oxidation reactions.