Spectroscopic investigation of the Dergaon meteorite with reference to 10 μm and 20 μm bands

Analysis of a part of the meteorite which fell at Dergaon (India) on March 2, 16.40 local time (2001) is presented with the help of FTIR, absorption and atomic spectra. The FTIR spectrum exhibits prominent absorption bands in the region 800–1100 cm⁻¹, originating from the valence vibration of SiO⁴, a basic component of the silicate lattice.     

Novel gallium-mediated C3-allylation of indoles and pyrroles in aqueous media promoted by Bu4NBr

A mild and efficient protocol for the coupling of indoles and pyrroles with allyl halides such as allyl bromide, crotyl bromide and propargyl bromide in the presence of gallium metal in a Bu₄NBr-DMF-H₂O system has been developed. The reaction is equally effective when cadmium is used in lieu of gallium and the corresponding 3-allyl indoles and 3-allyl pyrroles were obtained in almost comparable yields.     

Premicellar and micelle formation behavior of aqueous anionic surfactants in the presence of triphenylmethane dyes: protonation of dye in ion pair micelles

The premicellar and micelle formation behaviors of four cationic triphenylmethane dyes, viz, Pararosaniline (RN), Crystal violet (CV), Ethyl violet (EV), and Malachite green (MG), in aqueous anionic surfactant solutions of sodium dodecyl sulfate (SDS), sodium dodecyl benzene sulfonate (SDBS), and sodium dodecyl sulfonate (SDSN) have been studied by spectral and surface tension measurements. The study was carried out within a pH range where the dyes are stable in their quinoid forms. The dyes have been found to form dye–surfactant ion pairs (DSIPs) with the surfactants, at the surfactant concentrations well below their critical micelle concentration, CMC*. The DSIPs behave like nonionic surfactants and form an air–water interfacial monolayer. The DSIPs have a lower critical micelle concentration (CMC_IP), greater efficiency, and lower effectiveness than the corresponding pure surfactants. As the surfactant concentration is increased below the CMC*, the DSIPs start forming micelles of their own where the dye gets protonated and exists as a protonated dye–surfactant ion pair (PDSIP) in the ion pair micelles. As the concentration of the surfactant exceeds the CMC* of the pure surfactant, the protonation reverses gradually with the dye remaining in the micelles in solubilized form and the DSIPs in the air–water interfacial monolayer are replaced by pure surfactants. The distorted helical isomeric form (isomer B) of the dyes is favored in the PDSIPs. Copyright © 2009 John Wiley & Sons, Ltd.     

Hetero-Polar Sextuple Bond: A Relativistic Quantum Chemical Study**

Number of bonds formed by sharing an electron pair between two atoms is not restricted to one, it can go beyond four and six is the maximum. While homopolar sextuple bond in Mo₂ and W₂ has been reported, such a high bond order in heteropolar diatomics has remained elusive. In the pursuit of the sextuple bond in polar diatomics, the present study depicts the existence of such multiple bonds in Rhodium-Scandium hetero-diatom based on relativistic quantum chemical calculations. The bonding comprises of three normal electron sharing covalent bonds and three dative covalent bonds.     

A comparative study on structural,morphological and luminescence characteristics of Zn3(VO4)2 phosphor prepared via hydrothermal and citrate-gel combustion routes

Comparison of structural, morphological and spectroscopic properties of zinc vanadate Zn₃(VO₄)₂ phosphor synthesized via two different methods, viz. citrate-gel combustion and hydrothermal reaction, is presented. Highly crystalline and pure phase micro-rods are achieved by citrate-gel combustion route. The hydrothermal reaction products exhibit ribbon like structures. X-ray photoelectron spectroscopic investigation reveals the presence of multiple oxidation states of vanadium in the hydrothermally synthesized phosphor. Luminescence properties have also been compared and the effect of divalent cationic substitution (Ca, Mg) is presented.     

Green chemistry approaches to the regioselective synthesis of spiro heterobicyclic rings using iodine as a new and efficient catalyst under solvent-free conditions

Abstract  

Iodine catalyzes the pseudo four-component reaction of an aldehyde, a urea or thiourea, and cyclic 1,3-dicarbonyl compounds under microwave irradiation in a solvent-free condition to yield various σ symmetric spiro heterobicyclic rings in excellent yields.     

Preparation of phenolic compounds through catalyst-free ipso-hydroxylation of arylboronic acids

A novel method for the preparation of phenolic compounds through ipso-hydroxylation of the corresponding widely available arylboronic acid precursors is described. Through application of a novel PEG400-H₂O₂ reactant system, a variety of substituted phenols and other aromatic analogues have been prepared in excellent yields at room temperature in the absence of any catalyst.     

Iodine-Catalyzed Highly Effective Pictet–Spengler Condensation: An Efficient Synthesis of Tetrahydro-β-carbolines

Molecular iodine was found to be an efficient catalyst for the two-component Pictet–Spengler condensation of tryptamine with aldehydes, which leads to the formation of tetrahydro-β-carbolines in high yields.     

Improved Sensing of Capsaicin with TiO2 Nanoparticles Modified Epoxy Graphite Electrode

The presented research focuses on the electrochemical determination of capsaicin, a lipophilic alkaloid which originates hotness in chili peppers. An electrochemical sensor based on epoxy‐graphite composite with the modification of titanium dioxide (TiO₂) nanoparticles is developed for the determination of this alkaloid. The measurements were carried out in glycine buffer at pH 2.5 using cyclic voltammetry. Two linear concentration ranges were obtained from 6 to 75 μM (R=0.99) and from 12 to 138 μM, with a detection limit of 5.34 μM and 11.3 μM capsaicin, for 1^st and 2^nd oxidation peak, respectively. The main advantage of developed sensor is its repeatability and robustness against fouling; the relative standard deviation (RSD) value was 2.53 % (n=10). This voltammetric sensing procedure has successfully been applied to quantify capsaicin in various real samples such as hot chili sauce and pharmaceutical preparations.