One-Pot Synthesis of Benzo[4,5]imidazo[1,2-a]pyrimidin-2-ones Using a Hybrid Catalyst Supported on Magnetic Nanoparticles in Green Solvents

The conversion of soluble polyoxometalate into insoluble polyoxometalate is considered to be one of the major challenges in synthetic organic chemistry. Here, polyoxometalate was bonded to the salt part of an organic branch immobilized on the silica-coated Fe₃O₄ nanoparticle and characterized using various techniques. The fabricated complex was used as a heterogeneous catalyst in a novel one-pot reaction for synthesis of benzo[4,5]imidazo[1,2-a]pyrimidin-2-ones using aromatic amines, dimethyl acetylenedicarboxylate (DMAD), derivatives of benzaldehyde and 2-aminobenzimidazole in water/ethanol as a green solvent. 21 derivatives of benzo[4,5]imidazo[1,2-a]pyrimidin-2-one were synthesized by this method and fully characterized. The high stability of the catalyst showed that it can be reused for 6 times without decreasing in activity. The combination of new synthetic method, new ferromagnetic heterogeneous nano-catalyst, green solvent and simple separation method were presented in this work.     

Synthesis of 3,3‐Disubstituted Oxindoles via a Three‐Component Condensation Reaction in H2O

An efficient method has been developed for the synthesis of a novel series of unsymmetrically 3,3‐disubstituted oxindoles in good‐to‐high yields by a one‐pot three‐component condensation reaction of 2‐hydroxynaphthalene‐1,4‐dione, an isatin, and a barbituric acid derivative, in H₂O, and with p‐toluenesulfonic acid as a catalyst, at 90°. The effects of solvent, temperature, and the amount of catalyst on the yield of the reaction have been investigated. Additionally, the influence of hydrophilicity and hydrophobicity of the reactants on the selectivity of products has been examined.     

Kerr nonlinear switch based on ultra-compact photonic crystal directional coupler

In this paper, an all optical switch based on nonlinear photonic crystal directional coupler has been simulated and analyzed by the finite difference time domain (FDTD) method. The lunched pump signal increases the refractive indices of the central row of the coupler, due to nonlinear Kerr effect, hence the coupler works in the nonlinear conditions and lightwave guides to the other output port. We have tried to increase the coupling efficiency and reduce the required power in the nonlinear status by optimizing the bends structure and increasing the interaction between dielectric and lightwave signal. Therefore, the input signal beam can be controlled to be exchanged between two output ports to earn the highest output power ratio and the smallest amount of power required for nonlinear performance, the physical length of the coupler is determined to be 20a, where a is the structure lattice constant.     

A one-pot four-component synthesis of N-arylidene-2-aryl-imidazo[1,2-a]azin-3-amines

N-Arylidene-2-aryl-imidazo[1,2-a]azin-3-amines were synthesized via a one-pot, four-component condensation reaction using a 2-aminoazine, toluene-4-sulfonylmethyl isocyanide (TsCH₂NC), and two equivalents of readily available aromatic aldehydes. The reaction was performed in diethyl ether as the solvent, with p-toluenesulfonic acid (p-TSA) as the catalyst at reflux temperature.     

Effect of Synthesis Conditions on the Structural,Photocatalic, and Self-Cleaning Properties of TiO2 Nanoparticles

Physics of the Solid State - TiO2 nanoparticles were synthesized via the hydrothermal method. As-synthesized TiO2 properties were characterized by XRD, EDX, FESEM, FTIR, and UV-Vis spectroscopy....     

A new Navier–Stokes inverse method based on mass‐averaged tangential velocity for blade design

This paper presents a novel viscous inverse method for blade design. In this inverse design method the mass‐averaged tangential velocity and the blade thickness are prescribed, and the corresponding blade profile is sought. The blade profile is then computed iteratively using the discrepancies between the prescribed mass‐averaged tangential velocity distribution and its calculated distribution on an initial blade. The re‐design of an axial rotor blade, starting from an initial arbitrary profile in subsonic flow regimes, demonstrates the merits and robustness of this approach. Copyright © 2008 John Wiley & Sons, Ltd.     

Solvent polarity and hydrogen bond effects on nucleophilic substitution reaction of 2‐bromo‐5‐nitrothiophene with piperidine

The reaction kinetics of 2‐bromo‐5‐nitro thiophene with piperidine was studied in a solvent with a mixture of propan‐2‐ol with methanol and n‐hexane at 25°C. The measured rate coefficients of the reaction demonstrated dramatic variations in propan‐2‐ol–n‐hexane mixtures and mild variations in propan‐2‐ol–methanol system. The second‐order rate coefficients of the reaction, k_A, decreased sharply with n‐hexane content. The multiparameter correlation of log k_A versus molecular‐microscopic solvent parameters shows interesting results in these solutions. Linear free energy relationship investigations confirm that polarity has a major effect on the reaction rate and hydrogen bond ability of the media has a slight effect on the reaction rate. © 2011 Wiley Periodicals, Inc. Int J Chem Kinet 43: 185–190, 2011     

Description of complementary actions of mineral and organic additives in thermoplastic polymer composites by Flame Retardancy Index

This work visualizes the complementary actions of organic and mineral additives in model thermoplastic polymer composites in terms of Flame Retardancy Index (FRI). Thermal and flame retardancy behaviors of ethylene‐vinyl acetate copolymer (EVA) composites containing calcium carbonate (CC) mineral and ammonium polyphosphate (APP) organic additives were studied varying composition of additives in the 80/20 EVA/(xCC + (20 ? x)APP) composites with x denoting 0, 5, 10, 15, and 20 wt%. Thermogravimetric analysis (TGA) revealed that the onset temperature of composites and the remaining residue were increased by combination of APP and CC, while cone calorimetry results were indicative of a promising flame retardancy performance at a given composition of APP and CC. Based on FRI values, we made distinguished samples from flame retardancy performance viewpoint, where the best flame retardancy was obtained by combination of 15 wt% APP and 5 wt% CC, as reflected in FRI value of 3.08. By contrast, samples containing only APP or CC revealed low resistance against flame, as signaled by FRI values of 0.99 and 0.89, respectively. X‐ray diffraction (XRD) analysis was made on remaining residue collected at the end of cone calorimetry measurements. Moreover, Raman analysis confirmed barrier effect of flame retardancy for EVA/(5APP + 15CC) sample, featured by a higher graphitization level as well as a thicker yet more homogenous char layer. Mechanical behavior analysis of composites revealed an acceptable level of properties, particularly high elongation at break, which was almost independent of formulation. However, a minor loss in yield stress was observed, especially for EVA(10CC + 10APP) sample.     

Synthesis of a new series of multifunctional dialkyl 2-(1-(alkylamino)-1,3-dioxo-3-phenylpropan-2-yl)malonates as low molecular weight supramolecular organogelators using five-component reaction

Dialkyl 2-(1-(alkylamino)-1,3-dioxo-3-phenylpropan-2-yl)malonates have been synthesized using a one-pot, pseudo five-component condensation reaction of isocyanide, Meldrum's acid, phenylglyoxal and two alcohol molecules in CH₂Cl₂ at ambient temperature. It was found that these structures could be used as low molecular weight supramolecular organogelators. The gelation behaviors of these organic gelators have been investigated in various organic solvents. The results have shown that dioctyl 2-(1-(cyclohexylamino)-1,3-dioxo-3-phenylpropan-2-yl)malonate in n-dodecane is the best organogelator (0.2 wt%). Scanning electron microscopy and investigation of the rheological properties have indicated that gelator molecules create three dimensional networks via entangling self-assembled micro- and nano-rods. Hence the organogelation is induced by trapping solvent molecules in nano- and micro-spaces in the gel network.