Optical Emission and Raman Spectroscopy Studies of Reactivity of Low-Pressure Glow Discharges in Ar–O<Subscript>2</Subscript> and He–O<Subscript>2</Subscript> Gas Mixtures with Coked Catalysts

We demonstrate that low-pressure glow discharges in He–O₂ gas mixture are effective in removing carbonaceous surface layers from coked catalysts. These discharges contain a number of reactive species including O, O₃, and O₂*, and all these could contribute in the decoking process. However, an evolving understanding is that the O atoms in the discharge have a predominant role in this. A working hypothesis is that the O atoms react with the coke to form CO, CO₂ and other carbon complexes. Online measurements using emission spectra from O, H, and CO in the discharges are compared for the cases of He–O₂ and Ar–O₂ gas mixtures. Under the reported experimental conditions the estimated reactivity of the He–O₂ discharges is considerably higher compared with discharges in the Ar–O₂ gas mixture. Raman spectroscopy is used to confirm the removal of the coke from the surface of Pt/Alumina catalyst.     

l-Proline-catalysed one-pot synthesis of tetrahydrobenzo[c]acridin-8(7H)-ones at room temperature

Only 10 mol% of l-Proline in ethanol proved to be a very efficient catalyst for the one-pot synthesis of a wide variety of highly substituted tetrahydrobenzo[c]acridin-8(7H)-ones at room temperature. The key advantages of this process are high yields, cost effectiveness of the catalyst, easy work-up and the products can be directly recrystallized from hot ethanol.     

Novel isocyanide-based three-component reaction: a facile synthesis of substituted 1H-chromeno[2,3-d]pyrimidine-5-carboxamides

A mild and efficient method for the synthesis of 1H-chromeno[2,3-d]pyrimidine-5-carboxamide derivatives via a one-pot, three-component reaction of an isocyanide, barbituric acid, and a salicylaldehyde in the presence of acetic acid in ethanol/water mixture at 75 °C is reported. This high atom economy reaction led to the construction of one benzopyran ring, and one amide group in a single synthetic step.     

Cu(I)-catalyzed cascade reaction of N-tosylhydrazones with 3-butyn-1-ol: A new synthesis of tetrahydrofurans

The Cu(I)-catalyzed cascade coupling/cyclization reaction of N-tosylhydrazones with 3-butyn-1-ol has been explored. This new strategy represents a simple platform for the synthesis of tetrahydrofurans in moderate to good yields.     

Effects of length and number of aromatic rings in carboxylic acid ligands on structure and optical properties of lead(II) coordination polymers

Research on Chemical Intermediates - To systematically examine the effects of the length and number of aromatic rings in carboxylic acid ligands on the structure and properties of lead(II)...     

Toward a practical and waste-free synthesis of thioureas in water

An operationally simple and entirely green protocol for the synthesis of thiourea derivatives by the reaction of carbon disulfide with primary amines in pure water is developed. This reaction is a highly atom-economic process for production of highly pure, hindered thioureas without any catalyst and tedious work-up.     

Template-based growth of titanium dioxide nanorods by a particulate sol-electrophoretic deposition process

TiO 2 nanorods have been successfully grown into a track-etched polycarbonate (PC) membrane by a particulate sol-electrophoretic deposition from an aqueous medium.The prepared sols had a narrow particle size distribution around 17 nm and excellent stability against aging,with zeta potentials in the range of 47-50 mV at pH 2.It was found that TiO 2 nanorods were grown from dilute aqueous sol with a low,0.1-M concentration.Fourier transform infrared spectroscopy (FT-IR) analysis confirmed that a full conversi...     

Palladium-catalyzed stereoselective synthesis of 3-(aminomethylene)-oxindoles

An efficient palladium-catalyzed protocol for the stereoselective synthesis of 3-(aminoarylmethylene)-oxindoles has been developed. In this approach, Ugi-4-component reaction adducts were used as starting materials for carbopalladative cyclization-Buchwald reaction sequences.