Real‐time electro‐diffusion method to discriminate carbon nanomaterials

We report both the experimental and theoretical insights of differential electro‐diffusion behavior of carbon nanomaterials (e.g. single wall, multiwall carbon nanotubes, and graphene). We thus discriminate one from the other in a soft gel system. The differential mobility of such material depends on their intrinsic properties, both extend and rate of migration bearing the discriminatory signature. The mobility analysis is made by a real time monitoring of the respective bands.     

Synthesis,Chemical Characterization,DNA Interaction and Antioxidant,Studies of New Nitrosubstituted Thioureas and Their Copper Complexes

In the present work new nitro substituted thioureas, and their copper complexes have been synthesized and characterized by FTIR and multinuclear NMR techniques. Some of the compounds namely 1‐benzoyl‐3‐(4‐chloro‐3‐nitrophenyl) thiourea (A‐1), 1‐benzoyl‐3‐(4‐chloro‐3‐nitrophenyl) thiourea (A‐2) and 1‐benzoyl‐3‐(2‐methoxy‐4‐nitrophenyl) thiourea (A‐2) have also been characterized by single crystal XRD. All the synthesized compounds have been screened for DNA binding potencies (using cyclic voltametry, UV‐vis spectroscopy) and free radical scavanging activities.     

Exact solutions to magnetogasdynamic equations in Lagrangian coordinates

The Lie group of point transformations, which leave the equations for a simplified model of one dimensional ideal gas in magnetogasdynamics invariant, are used to obtain some exact solutions for the governing system of hyperbolic partial differential equations (PDEs). Similarity variables which reduces the governing system of PDEs into system of ordinary differential equations (ODEs) are determined through the transformations. The resulting ODEs are solved analytically to obtain some exact solutions that exhibits space-time dependence. Further, we study the propagation of weak discontinuity through a state characterized by one of the solutions.     

Poly(N-isopropylacrylamide)-grafted dual stimuli-responsive filter paper for protein separation

Thermal and salt dual stimuli-responsive filter-paper-based membranes were prepared by UV-induced grafting of NIPAM-based polymers on paper surface. The grafting ratio could be controlled by monomer concentration during grafting polymerization. The results from pressure drop measurement of the mobile phase flowed cross the membrane demonstrate that an appropriate grafting ratio would be 8%-10%. Protein adsorption on the membrane through hydrophobic interaction could be promoted by increasing temperature and lyotropic salt concentration. The effect of grafted polymer structure on protein binding performance was studied. Filter paper grafted with NIPAM-based branched copolymer consisting of hydrophobic monomer moieties shows ten times higher protein binding capacity than that of the original filter paper. The separation of plasma proteins using the dual stimuli-responsive membrane was examined to demonstrate feasible application for hydrophobic interaction chromatographic separation of proteins.     

Effect of heterocyclic ring system on formation of dimeric quinolones under catalyst-free conditions: a green approach

The intermediate-dependent green and efficient synthesis of dimeric quinolones 4a–l and 7a–l by the Knoevenagel condensation followed by Michael-type addition of 4-hydroxy-1-methylquinolin-2(1H)-one 1a, b to indole-3-aldehydes 2a–f and aromatic aldehydes 5a–l in water through the condensed compound 3a–l under catalyst-free conditions is described. This reaction was found to be environmentally friendly, has easy-workup and shorter reaction times giving good yields of the product without the need for its isolation using column chromatography.     

Design,synthesis, and antibacterial studies of potent pyrazolinyltriazoles

Research on Chemical Intermediates - A library of pyrazolinyltriazole hybrids (3a–l, 4a–l) was synthesized via azide–alkyne dipolar (Huisgen) cycloaddition of azidoacetyl...     

Modeling droplet dispersion and interphase turbulent kinetic energy transfer using a new dual-timescale Langevin model

Dispersion of spray droplets and the modulation of turbulence in the ambient gas by the dispersing droplets are two coupled phenomena that are closely linked to the evolution of global spray characteristics, such as the spreading rate of the spray and the spray cone angle. Direct numerical simulations (DNS) of turbulent gas flows laden with sub-Kolmogorov size particles, in the absence of gravity, report that dispersion statistics and turbulent kinetic energy (TKE) evolve on different timescales. Furthermore, each timescale behaves differently with Stokes number, a non-dimensional flow parameter (defined in this context as the ratio of the particle response time to the Kolmogorov timescale of turbulence) that characterizes how quickly a particle responds to turbulent fluctuations in the carrier or gas phase. A new dual-timescale Langevin model (DLM) composed of two coupled Langevin equations for the fluctuating velocities, one for each phase, is proposed. This model possesses a unique feature that the implied TKE and velocity autocorrelation in each phase evolve on different timescales. Consequently, this model has the capability of simultaneously predicting the disparate Stokes number trends in the evolution of dispersion statistics, such as velocity autocorrelations, and TKE in each phase. Predictions of dispersion statistics and TKE from the new model show good agreement with published DNS of non-evaporating and evaporating droplet-laden turbulent flow.     

Fluoro-substituted ketones from nitriles using acidic and basic reaction conditions

Fluoro-substituted aliphatic nitriles are shown to undergo the Houben-Hoesch reactions with arenes in CF₃SO₃H to give fluoro-substituted ketones in good yields. The fluorine substituents appear to enhance the reactivities of the nitriles (and the nitrilium ion intermediates) compared to similar aliphatic nitriles. Fluoro-substituted ketones are also shown to be accessible through the reactions of organometallic reagents and fluoro-substituted nitriles.     

Ru(III) complexes containing 3,5-pyrazole dicarboxylic acid and triphenylphosphine/triphenylarsine: Synthesis, characterization and catalytic activity

New hexa-coordinated Ru(III) complexes of the type [Ru(H₂Pzdc)(EPh₃)₃X₂] have been synthesized by reacting 3,5-pyrazole dicarboxylic acid (H₃Pzdc) with the appropriate starting complexes [RuX₃(EPh₃)₃] (where X = Cl or Br; E = P or As). The ligand behaves as a bidentate monobasic chelate. All the complexes have been characterized by analytical and spectroscopic (IR, electronic and EPR) data. Single-crystal X-ray analysis of the complex [Ru(H₂Pzdc)(PPh₃)₂Cl₂]·C₆H₆·C₂H₅OH revealed that the coordination environment around the ruthenium center consists of an NOP₂Cl₂ octahedron. The planar ligand occupies the equatorial position along with two chlorine atoms, while the triphenylphosphine groups occupy the axial positions. The electrochemical behavior of the new complexes was studied using cyclic voltammetry. The new mononuclear ruthenium complexes are capable of acting as catalysts for the oxidation of alcohols.