Mo (CO)6‐assisted Pd‐supported magnetic graphene oxide‐catalyzed carbonylation‐cyclization as an efficient way for the synthesis of 4(3H)‐quinazolinones

In this paper, a novel catalyst is introduced based on the immobilization of palladium on modified magnetic graphene oxide nanoparticles. The catalyst is characterized by several methods, including transmission electron microscopy, scanning electron microscopy, X‐ray fluorescence, vibrating‐sample magnetometer, Fourier transform‐infrared and dynamic light scattering (DLS) analysis. The activity of the catalyst was investigated in the synthesis of 4(3H)‐quinazolinones via Pd‐catalyzed carbonylation‐cyclization of N‐(2‐bromoaryl) benzimidamides by Mo (CO)₆. The Mo (CO)₆ is used as a carbon monoxide source for performing the reaction under mild conditions. The catalyst showed good reusability, and no change in activity was observed after 10 cycles of recovery.     

Selective oxidation of alcohols over nickel zirconium phosphate

Nickel zirconium phosphate nanoparticles were found to function as efficient catalysts for the selec-tive oxidation of a wide range of alcohols to their corresponding ketones and aldehydes using H2O2 as an oxidizing agent and without any organic solvents, phase transfer catalysts, or additives. The steric and electronic properties of various substrates had significant influence on the reaction con-ditions required to achieve acetylation. The results showed that this method can be applied for the chemoselective oxidation of benzyl alcohols in the presence of aliphatic alcohols. The catalyst used in the current study was characterized by ICP-OES, XRD, NH3-TPD, Py-FTIR, N2 adsorp-tion-desorption, SEM and TEM. These analyses revealed that the interlayer distance in the catalyst increased from 0.75 to 0.98 nm when Ni2+ was intercalated between the layers, whereas the crystal-linity of the material was reduced. The nanocatalyst could also be recovered and reused at least seven times without any discernible decrease in its catalytic activity. This new method for the oxi-dation of alcohols has several key advantages, including mild and environmentally friendly reaction conditions, short reaction time, excellent yields and a facile work-up.     

Magnetic solid-phase extraction of imatinib and doxorubicin as cytostatic drugs by Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>/graphene oxide nanocomposite

Magnetic solid-phase extraction based on Fe₃O₄/graphene oxide nanocomposites was investigated for the separation, preconcentration and determination of imatinib and doxorubicin in aqueous solutions. Synthesis of Fe₃O₄/graphene oxide was characterized by transmission electron microscopy, energy-dispersive X-ray analyzer and vibrating sample magnetometer. After optimizing the conditions, optimal experimental conditions including sample pH, the amount of the magnetic nanoparticles, the effect of salt concentration and other chemotherapy medications, eluent type and extraction time were studied and established. The method showed good linearity for the determination of doxorubicin and imatinib in the concentration range of 0.01–100 μg mL^?1 in aqueous solutions with limit of detection 1.8 ng mL^?1 for doxorubicin and 1.9 ng mL^?1 for imatinib. The relative recoveries of doxorubicin and imatinib levels were 96.7 and 88.4%, respectively. The results indicate that the present procedure is a suitable method for extraction of imatinib and doxorubicin from environmental water samples.     

Determination of nickel in natural waters by FAAS after sorption on octadecyl silica membrane disks modified with a recently synthesized Schiff's base

A simple, highly sensitive, accurate and selective method for the determination of trace amounts of Ni²⁺ ions in water samples is proposed. The method is based on the separation and preconcentration of Ni²⁺ on an octadecyl-bonded silica (ODBS) membrane disk modified by a recently synthesized Schiff’s base N,N′-bis (3-methylsalicylidene) ortho phenylene diamine (MSOPD) at pH 7. The synthesis of this extractant ligand is also described. The retained nickel on the membrane was eluted with 2×5 ml 0.5 M HNO₃ and measured by flame atomic absorption spectrometry (FAAS) at 232.0 nm. The extraction efficiency and the influence of the type and least amount of eluent for the stripping of Ni²⁺ from the disks, pH, flow rates of sample solution and eluent, amount of MSOPD, effect of other ions, and breakthrough volume were evaluated. The maximum capacity of the membrane disks modified by 3 mg of MSOPD was found to be 146±4 μg Ni²⁺. The 3σ limit of detection of the method was 30 ng per 1000 ml and also an enrichment factor of 250 was obtained. The proposed method has been applied to the determination of nickel in several water samples with satisfactory results.     

Comparison between decoherence time for a two-state spin ½ system with its corresponding quantum retrieval period

The evolution of a two-state quantum system (a spin ½ particle) in both the framework of standard quantum mechanics and under the decoherence regime is considered. The former approach on this issue is the well-known quantum flipping process of a dichotomic system subjected to a time-dependent magnetic field. In the latter approach, the Spin-Boson model is utilized to describe the interaction of system with its environment and the Born-Markov master equation is derived to obtain the decoherence time. It is possible to show that under certain conditions, one may find a potential conflict between the predictions of decoherence theory and the result observed in a typical quantum flipping experiment.     

Two‐dimensional prediction of time dependent,turbulent flow around a square cylinder confined in a channel

This paper presents two‐dimensional and unsteady RANS computations of time dependent, periodic, turbulent flow around a square block. Two turbulence models are used: the Launder–Sharma low‐Reynolds number k–ε model and a non‐linear extension sensitive to the anisotropy of turbulence. The Reynolds number based on the free stream velocity and obstacle side is Re=2.2×10⁴. The present numerical results have been obtained using a finite volume code that solves the governing equations in a vertical plane, located at the lateral mid‐point of the channel. The pressure field is obtained with the SIMPLE algorithm. A bounded version of the third‐order QUICK scheme is used for the convective terms. Comparisons of the numerical results with the experimental data indicate that a preliminary steady solution of the governing equations using the linear k–ε does not lead to correct flow field predictions in the wake region downstream of the square cylinder. Consequently, the time derivatives of dependent variables are included in the transport equations and are discretized using the second‐order Crank–Nicolson scheme. The unsteady computations using the linear and non‐linear k–ε models significantly improve the velocity field predictions. However, the linear k–ε shows a number of predictive deficiencies, even in unsteady flow computations, especially in the prediction of the turbulence field. The introduction of a non‐linear k–ε model brings the two‐dimensional unsteady predictions of the time‐averaged velocity and turbulence fields and also the predicted values of the global parameters such as the Strouhal number and the drag coefficient to close agreement with the data. Copyright © 2009 John Wiley & Sons, Ltd.     

Synthesis,characterization, and molecular structures of Ni(II) and Cd(II) complexes derived from dithiophosphonate

Two novel dithiophosphonate ligands, HS₂P(p‐C₆H₄OMe)(OCH₂CH₂CH(CH₃)₂) ( 1 ) and HS₂P(p‐C₆H₄OMe)(OCH(CH₃)₂) ( 2 ), were synthesized and characterized by multinuclear (¹H, ³¹P, and ¹³C) NMR, infrared spectroscopy as well as elemental analysis. The reactions of 1 and 2 with NiCl₂·6H₂O and Cd(NO₃)₂·4H₂O in methanol led to novel complexes 3 and 4 . The single crystal X‐ray structures of 3 and 4 showed tetracoordinated structure with square planar geometry for the nickel complex, while it showed pentacoordinated structure with distorted square‐pyramid environment for the cadmium complex.     

An unexpected coupling reaction between isocyanides and carboxylic acids: a method for the synthesis of highly stable symmetrical and unsymmetrical alkylamidine and arylamidine carbocations

An unexpected coupling reaction between isocyanides and carboxylic acids which led to the synthesis of highly stable symmetrical and unsymmetrical alkylamidine and arylamidine carbocations under mild reaction conditions is described. The structures of these compounds were confirmed by IR, mass, ¹H NMR, ¹³C NMR, and single-crystal X-ray diffraction studies and a plausible mechanism is proposed.     

Recent progress of isocyanide-based multicomponent reactions in Iran

The aim of this review is to provide an overview of the contributions and recent advances made by Iranian scientists in the field of isocyanide-based reactions between 1999 and 2009. With over 100 publications during this period, Iranians are responsible for approximately 10% of all publications in the world involving isocyanide-based multicomponent reactions (IMCRs). Some important aspects of these IMCRs include the execution of reactions in green reaction mediums like water or ethanol, high atom economies, mild reaction conditions, high yields, and catalyst-free processes. On the other hand, in most of these reactions, new classes of heterocyclic compounds with potential biological and medicinal activities have been reported.