The mechanism of aromatic nucleophilic substitution reaction between ethanolamine and fluoro‐nitrobenzenes: an investigation by kinetic measurements and DFT calculations

We have studied the kinetics and elucidated the mechanism by DFT calculation of the reaction between ethanolamine (EOA) and 1‐fluoro‐2,4‐dinitrobenzene (DNFB) in acetonitrile and toluene. To determine the contribution of the nitro group, the activation energy of the reaction between ethanolamine and 1‐fluoro‐2‐nitrobenzene (MNFB) vs. DNFB was determined in acetonitrile and calculated by DFT method. Kinetic measurements reveal that the reaction is faster in acetonitrile than in toluene. The reaction follows overall second‐order kinetics: first order with respect to both EOA and DNFB which is similar to the results reported for reaction between other primary amines and 1‐substituted‐2,4‐dinitrobenzenes. The calculations by using DFT methods reveal that the mechanism of the reaction involves the formation and decomposition of a Meisenheimer complex (MC). DFT calculations also reveal that the activation energy of the reaction is highest in vacuum and decreases with increasing polarity of the solvent reaching a minimum in acetonitrile. In addition, activation energies obtained by both DFT calculations and experiments show that the reactivity of MNFB is less than that of DNFB showing the effect of the 4‐nitro group. Copyright © 2010 John Wiley & Sons, Ltd.     

Predicting extrusion instabilities of commercial polyethylene from non-linear rheology measurements

Processing at the highest possible throughput rates is essential from an economical point of view. However, various flow instabilities and extrudate distortions like sharkskin, stick slip, and gross melt fracture (GMF) may limit the production rate of high-quality products. Predicting the process conditions leading to the occurrence of rheological instabilities is the key for improving product quality, process control, and optimization. Large-amplitude oscillatory shear (LAOS) and FT-rheology were used to quantify the non-linear rheological behavior and instabilities of a series of well-characterized commercial polyethylene (PE). From the latter, we derive the critical non-linearity parameter, F _0,c, which corresponds to the normalized intensity of the third harmonic at the critical strain amplitude, γ _0,C (defined by the appearance of the second harmonic), normalized by γ _0,C . The F _0,c is correlated with the high molecular mass fraction of the polymers and with the Deborah numbers. Linear rheological parameters and molecular structures were related to F _0,c. An experimental correlation between F _0,c of commercial PE melts and pressure fluctuations associated with flow instabilities (sharkskin) was established both for capillary rheometry and extrusion.     

Understanding the Photoluminescence Mechanism of Nitrogen‐Doped Carbon Dots by Selective Interaction with Copper Ions

Doped fluorescent carbon dots (CDs) have drawn widespread attention because of their diverse applications and attractive properties. The present report focusses on the origin of photoluminescence in nitrogen‐doped CDs (NCDs), which is unraveled by the interaction with Cu²⁺ ions. Detailed spectroscopic and microscopic studies reveal that the broad steady‐state photoluminescence emission of the NCDs originates from the direct recombination of excitons (high energy) and the involvement of defect states (low energy). In addition, highly selective detection of Cu²⁺ is achieved, with a detection limit of 10 μm and a dynamic range of 10 μm –0.4 mm . The feasibility of the present sensor for the detection of Cu²⁺ in real water samples is also presented.     

Unusual coordination mode of tetradentate Schiff base cobalt(III) complexes

Contrary to the stereotype, Jacobsen's catalyst, chiral (salcy)Co(III)OAc adopts an unusual binding mode. The tetradentate {ONNO} ligand does not form a square plane but wraps cobalt in a cis-β fashion while acetate is chelating.     

Reactions of Organic Ions at Ambient Surfaces in a Solvent-Free Environment

Solvent-free ion/surface chemistry is studied at atmospheric pressure, specifically pyrylium cations, are reacted at ambient surfaces with organic amines to generate pyridinium ions. The dry reagent ions were generated by electrospraying a solution of the organic salt and passing the resulting electrosprayed droplets pneumatically through a heated metal drying tube. The dry ions were then passed through an electric field in air to separate the cations from anions and direct the cations onto a gold substrate coated with an amine. This nontraditional way of manipulating polyatomic ions has provided new chemical insights, for example, the surface reaction involving dry isolated 2,4,6-triphenylpyrylium cations and condensed solid-phase ethanolamine was found to produce the expected N-substituted pyridinium product ion via a pseudobase intermediate in a regiospecific fashion. In solution however, ethanolamine was observed to react through its N-centered and O-centered nucleophilic groups to generate two isomeric products via 2H-pyran intermediates. The O-centered nucleophile reacted less rapidly to give the minor product. The surface reaction product was characterized in situ by surface enhanced Raman spectroscopy, and ex situ using mass spectrometry and H/D exchange, and found to be chemically the same as the major pyridinium solution-phase reaction product.     

Nanoparticles-chemistry, new synthetic approaches, gas phase clustering and novel applications

In this paper, an overview of the synthesis, chemistry and applications of nanosystems carried out in our laboratory is presented. The discussion is divided into four sections, namely (a) chemistry of nanoparticles, (b) development of new synthetic approaches, (c) gas phase clusters and (d) device structures and applications. In ‘chemistry of nanoparticles’ we describe a novel reaction between nanoparticles of Ag and Au with halocarbons. The reactions lead to the formation of various carbonaceous materials and metal halides. In ‘development of new synthetic approaches’ our one-pot methodologies for the synthesis of core-shell nanosystems of Au, Ag and Cu protected with TiO₂ and ZrO₂ as well as various polymers are discussed. Some results on the interaction of nanoparticles with biomolecules are also detailed in this section. The third section covers the formation of gas phase aggregates/clusters of thiol-protected sub-nanoparticles. Laser desorption of H₂MoO₄, H2WO₄, MoS₂, and WS₂ giving novel clusters is discussed. The fourth section deals with the development of simple devices and technologies using nanomaterials described above.     

Quantum Dots (QDs) Based Fluorescent Sensor for the Selective Determination of Nimesulide

Fluorescent PET (Photoinduced Electron Transfer) has been of particular growth in recent times. A novel PET based fluorescent sensor using unmodified CdSe quantum dots (QDs) has been developed for the trace determination of Nimesulide (NIM). The sensor is based on the selective fluorescence quenching of quantum dots by NIM in presence of other NSAIDs and is found that intensity of quenching is linearly related to NIM concentration in the range 8.2?×?10^?7 – 4.01?×?10^?5?M. The mechanism of interaction is discussed. Finally, the potential application of the proposed method for the trace determination of NIM in pharmaceutical formulation is demonstrated.     

Magnetic Moment and Susceptibility Measurements of Mixed Rare Earth Oxalate Crystals

The growth of double rare earth oxalate crystals with a general chemical formula AB(C₂O₄)₃ · 10 H₂O (where A and H are Nd, Pr and Sm) is reported. The variation of the magnetic moment of these crystals with an external field is studied and the magnetic susceptibility and the effective magnetic moment are calculated. The observed effective magnetic moment of the crystals are in good agreement with those calculated on theoretical grounds.     

Structural and spectroscopic investigations on the quenching free luminescence of europium oxalate nanocrystals

The structural features leading to the intense quenching free luminescence exhibited by europium oxalate nanocrystals, poly[[hexaaquatri‐μ₂‐oxalato‐dieuropium] 4.34‐hydrate], {[Eu₂(C₂O₄)₃(H₂O)₆]·4.34H₂O}_n, is the focal point of this report. Europium oxalate nanocrystals were synthesized by a simple microwave‐assisted co‐precipitation method. Powder X‐ray diffraction analysis revealed the monoclinic structure of the nanocrystals and the phase purity. The morphology and particle size were examined by transmission electron microscopy (TEM) analysis. Luminescence measurements on a series of samples of La_2–xEu_x(C₂O₄)₃·10H₂O, with x varying in the range 0.1 to 2, established the quenching free nature exhibited by the europium oxalate nanocrystals. A single‐crystal structure analysis was carried out and the quenching free luminescence is explained on the basis of the crystal structure. A detailed photoluminescence characterization was carried out using excitation and emission studies, decay analysis, and CIE coordinate and colour purity evaluation. The various spectroscopic parameters were evaluated by Judd–Ofelt theoretical analysis and the results are discussed on the basis of the crystal structure analysis.