Experimental Investigations on the Thermal Diffusion Characteristics and Photoluminescence in Multiphase Micro Fluids Containing ZnO Micro Tubes and Fluorescein Dye

Optics and Spectroscopy - Scattering of light by disordered structures is normally detrimental to their applicability in many optoelectronic devices. However, some micro and nanostructures are...     

PAMAM Dendrimers as Anchors for the Preparation of Electrocatalytically Active Ultrathin Metallic Films

This paper describes the formation of catalytically active thin films of Pt, Pt/Au, and Pt/Ru on gold substrates stabilized by amine‐terminated polyamidoamine (PAMAM) dendrimers. A monolayer of dendrimer is initially self‐assembled on the gold substrate, which serves as a template for the growth of catalytically active thin films. As dendrimers contain tens to hundreds of functional groups at the periphery, the aggregate strength of the multidentate interactions with the gold substrate leads to the formation of robust films. The films were found to exhibit high catalytic activity for the oxidation of small hydrocarbons such as methanol. Such films offer versatility and scope for the design of effective electrocatalysts, especially in the context of microfuel cells and “dendrichips”; hence, they could find applications in the fields of sensors, fuel cells, and waste‐water treatment.     

Mixed-ligand chelate extraction of neodymium(III) with thenoyltrifluoroacetone and various sulphoxides

Mixed-ligand chelate extraction of Nd(III) into benzene with mixtures of thenoyltrifluoroacetone (HTTA) and bis-2-ethylhexyl sulphoxide (B2EHSO) or di-n-octyl sulphoxide (DOSO) or diphenyl sulphoxide (DPhSO) or trioctylphosphine oxide (TOPO) from thiocyanate solutions has been studied. A very high synergistic enhancement of the order 10(3) has been observed in these systems. Thus this mixed-ligand chelate system may be useful in the extraction and separation of Nd(III) from other metal ions. The mechanism of extraction can be explained by a simple chemically based model presented in this paper.     

Epoxidation and oxidation reactions using 1,4-butanediol dimethacrylate crosslinked polystyrene-supported tertiary butyl hydroperoxide

1,4-Butanediol dimethacrylate (1,4-BDDMA) crosslinked polystyrene-supported t-butyl hydroperoxide was employed in the epoxidation of olefins and oxidation of alcohols to carbonyl compounds. The reagent proved to be successful as a recyclable solid phase organic reagent with as much or more efficiency when compared to its monomeric counterpart. The extent of reaction was found to be dependent on various reaction parameters like solvent, temperature, molar concentration and presence of catalyst.     

Taguchi orthogonal design assisted immobilization of Candida rugosa lipase onto nanocellulose-silica reinforced polyethersulfone membrane: physicochemical characterization and operational stability

Cellulose - A greener processing route to replace the current environmentally-unfriendly esterification technique to produce biofuels such as pentyl valerate (PeVa) was explored. This study...     

Synthesis and Bioassay of Ethyl-2- (2-((Diethoxyphosphoryl) (Aryl) Methylamino)Thiazol-4-Yl)-2-(Methoxyimino)Acetates

Abstract

A simple, efficient, and environmentally benign methodology has been accomplished for the synthesis of α-aminophosphonates by one-pot three-component reaction of ethyl-2-amino-α-(methoxy-imino)-4-thiazoleacetate, aldehydes, and diethylphosphite by using Amberlyst-15 as catalyst at room temperature under solvent-free conditions. Their chemical structures were characterized by infrared (IR), NMR (¹H, ¹³C & ³¹P), mass spectral, and elemental analysis. All the title compounds were screened for radical-scavenging activity by 1,1-diphenyl-2-picrylhydrazyl (DPPH), nitic oxide (NO), and hydrogen peroxide (H₂O₂) methods.

Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements for the following free supplemental files: Additional text and figures.     

Molybdenum Catalyzed Protective Tetrahydropyranylation of Alcohols and Phenols

Molybdenyl(VI) acetylacetonate is an effective catalyst for the protective tetrahydropyranylation of alcohols and phenols.     

Lignite fired fly ash modified by chemical treatment for adsorption of zinc from aqueous solution

The purpose of the study described in this paper was to compare removal of Zn(II) from aqueous solutions by use of two adsorbents—alkali-modified fly ash (FAN) and alkali and dye-modified fly ash (FAN-MO). The effects of four conditions (solution pH, contact time, initial metal ion concentration, and dose of adsorbent) on removal of Zn(II) at 27 ± 5 °C were studied in batch mode. Adsorption of Zn(II) was greater at pH 4.0 for FAN (76.49 %) and at pH 5.0 for FAN-MO (24.72 %). Maximum adsorption of Zn(II) by FAN and FAN-MO was achieved after 50 min. The linear forms of the Langmuir, Freundlich, Tempkin, D–R, Harkin–Jura, and Frenkel–Halsey isotherms were used for experiments with different concentrations of the metals. Adsorption of Zn(II) ions satisfied the Langmuir isotherm model only. The adsorption capacity of both adsorbents was also investigated by column studies. Adsorption of Zn(II) ions on FAN in column studies (45.33 %) was lower than in batch mode studies. For FAN-MO, adsorption was 37.88 % in column studies, again lower than in batch mode studies. Fly ash modified by alkali had a higher adsorption capacity for Zn(II) ions than fly ash modified by alkali followed by addition of dye.     

Synthesis and in vitro antimicrobial studies of thiodihydropyrimidine derivatives

In the present study, a series of thiodihydropyrimidine derivatives were synthesized from different substituted aromatic aldehydes, ethyl acetoacetate, and urea/thiourea using a bimetallic TUD-1 catalyst. The structures of all the synthesized compounds were characterized by melting point determination, thin layer chromatography (TLC), infrared (IR), ¹HNMR, and ¹³C-NMR values. All the synthesized compounds were screened for their antimicrobial activities against two gram positive bacteria, two-gram negative bacteria, and two fungal strains.     

A quick and regioselective access of spirooxindole-oxazoline by reaction of isatin and isocyanoacetate “on water”

A greener, rapid and regioselective “on water” synthesis of spirooxindole-oxazoline by the reaction of isatin and isocyanoacetate at room temperature is described. The developed protocol has the advantage of being atom-economical, eco-friendly, and benign reaction conditions. Broader substrate scope, experimentally simple procedures, and easy purification of products with high yield further make this method attractive. The synthesized compounds have been fully characterized with spectral analysis.