[Et3N-SO3H][MeSO3] as a highly efficient catalyst for the production of pyrido[2,3-d:6,5-d′]dipyrimidines and bis(pyrazolyl)methanes

Research on Chemical Intermediates - In this research, highly efficient protocols for the production of pyrido[2,3-d:6,5-d′]dipyrimidine and bis(pyrazolyl)methane derivatives using an acid...     

Immobilized metalloporphyrins on 3-aminopropyl-functionalized silica support as heterogeneous catalysts for selective oxidation of primary and secondary alcohols

Abstract  

Iron(III), manganese(III), and cobalt(II) complexes of meso-tetrakis(p-chlorophenyl)porphyrin (Fe(TClPP)X, Mn(TClPP)X, and Co(TClPP)X, X = Cl or OAc) were immobilized onto 3-aminopropyl-functionalized silica (SF-3-APTS). SF-3-APTS acts as both axial base and support for immobilization of these metalloporphyrins. The obtained heterogeneous catalysts were characterized by Fourier transform infrared (FT-IR), UV–Vis, and inductively coupled plasma (ICP) spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), and thermogravimetric analysis (TGA) techniques. Their catalytic activity as biomimetic catalysts was investigated for the selective oxidation of primary and secondary benzylic alcohols to the corresponding carbonyl compounds with t-butylhydroperoxide as oxidant. SF-3-APTS–Fe(TClPP)Cl demonstrated higher catalytic activity than SF-3-APTS–Mn(TClPP)Cl and SF-3-APTS–Co(TClPP)OAc. The presence of electron-withdrawing substituents on benzylic alcohols enhances the rate of catalytic oxidation. SF-3-APTS–Fe(TClPP)Cl could be reused at least four times without significant loss of its catalytic activity.     

Uranyl sensor based on a N,N′-bis(salicylidene)-2-hydroxy-phenylmethanediamine and multiwall carbon nanotube electrode

The electrochemical determination of uranyl was investigated by using carbon paste electrode modified with a Schiff base namely N,N??-bis(salicylidene)-2-hydroxy-phenylmethanediamine (SHPMD/CPE) and also in the presence of carbon nanotube (SHPMD/CNT/CPE). The both modified electrodes displayed an irreversible peak at E _pa?=?0.798?V versus Ag/AgCl. The electrocatalytic reduction of uranyl has been studied on SHPMD/CNT/CPE, using cyclic and differential pulse voltammetry, chronocoulometry and linear sweep techniques. Electrochemical parameters including the diffusion coefficient (D), the electron transfer coefficient (??), the ionic exchange current (i) and the redox reaction rate constant (K) were determined for the reduction of uranyl on the surface of the modified electrodes. Linear range concentration is 0.002?C0.6???mol?L^?1 and the detection limit of uranyl is 0.206?nmol?L^?1. The proposed method was used to detect uranyl in natural waters and good recovery was achieved.     

Electrochemical determination of tyrosine in the presence of uric acid at a carbon paste electrode modified with multi-walled carbon nanotubes enhanced by sodium dodecyl sulfate

Tyrosine (Tyr) was quantitated with high sensitivity and selectivity in the presence of uric acid (UA) using a carbon paste electrode modified with multi-walled carbon nanotubes. Tyr and UA were catalytically oxidized with diffusion-controlled characteristics. They were determined simultaneously by differential pulse voltammetry with a potential difference of 350 mV. The electrocatalytic currents increase linearly with Tyr and UA concentrations 4×10^?7?1×10^?4 M and 3×10^?7?2×10^?4 M. Their detection limits were 1×10^?7 and 5.1×10^?8 M respectively. In the presence of sodium dodecyl sulfate the Tyr detection limit improved from 1×10^?7 to 6.9×10^?8 M. The electrode was successfully used to quantitate Tyr and UA in serum.      

Electrochemical determination of acetaminophen in the presence of propranolol using an electrode modified with a Schiff base from 2-hydroxy-1-naphthaldehyde and ethylenediamine and multi-walled carbon nanotubes

A carbon paste electrode, modified with N,N′-bis-(2-hydroxy-1-naphthalidene)ethylenediamine and multi-walled carbon nanotubes (HNED-MWCNPE), was used for the determination of acetaminophen (ACOP) and propranolol (PP). Cyclic voltammetry (CV), chronocoulometry, chronoamperometry and differential pulse voltammetry (DPV) techniques were employed to study electro-oxidation of ACOP. The results revealed that the modified electrode showed an electrocatalytic activity toward the anodic oxidation of acetaminophen by a marked enhancement in the current response in buffered solution at pH 8.0. Some kinetic parameters such as the electron transfer coefficient (α) were also determined for the ACOP oxidation. The linear concentration range of 1 × 10^?3?1 × 10^?6 M with a detection limit of 4.6 × 10^?8 M (n = 16) for ACOP was obtained using DPV (pH 8.0). The modified electrode shows good sensitivity, selectivity and stability. The prepared electrode was also applied for the determination of ACOP in human blood serum.     

A simple model for a two-stage chemical reaction with diffusion

We analyse the evolution of a two-stage chemical reaction betweentwo neighbouring plumes of reactants. Under the assumption thatthe plumes are approximately Gaussian we derive a system ofordinary differential equations for the total amount, the centroidand the variance of each reactant. We compare the solution ofthese equations with full numerical simulation of the reaction.Excellent agreement is obtained, with solution of the near-Gaussianmodel requiring considerably less computational effort thanthe full simulations. Of key importance is the yield of thereaction, and we discuss this feature in particular.     

The L<Superscript>2</Superscript>-convergence of the Legendre spectral Tau matrix formulation for nonlinear fractional integro differential equations

The operational Tau method, a well known method for solving functional equations is employed to approximate the solution of nonlinear fractional integro-differential equations. The fractional derivatives are described in the Caputo sense. The unique solvability of the linear Tau algebraic system is discussed. In addition, we provide a rigorous convergence analysis for the Legendre Tau method which indicate that the proposed method converges exponentially provided that the data in the given FIDE are smooth. To do so, Sobolev inequality with some properties of Banach algebras are considered. Some numerical results are given to clarify the efficiency of the method.     

Gas-phase deprotonation of arylalkylamines. A collision-induced dissociation study

The collision-induced dissociation (CID) of deprotonated arylalkylamines of general formula R(1)C(6)H(4)CHR(2)CH(2)NR(3)(2) (where R(1) = H, OH, F or NO(2); R(2) = H or OH; R(3) = H or CH(3)) generated by negative chemical ionization with H(2)O and D(2)O as ionizing reagents, is discussed. The negative chemical ionization mass spectra show that, in the absence of a hydroxy group in the aromatic ring, deprotonation takes place at the benzylic position whereas the proton is lost from the OH group when present. The nitro compound forms only M(-.) ions. The CID spectra of the deprotonated molecules show that fragmentations are strongly dependent on the structural features of the molecules, namely the presence or absence of substituents in the aromatic ring or aliphatic chain. Copyright 1999 John Wiley & Sons, Ltd.     

Facile and eco-benign synthesis of a novel MnFe2O4@SiO2@Au magnetic nanocomposite with antibacterial properties and enhanced photocatalytic activity under UV and visible-light irradiations

The purpose of this research is to prepare novel, inexpensive, eco-friendly and efficient magnetic nanocomposites for degradation of pollutant from wastewater and their potential antibacterial activity. To reach this goal, we have synthesized magnetic MnFe₂O₄@SiO₂@Au (MnFe@Si@Au) nanocomposites through ultrasound assisted co-precipitation technique in presence of carbohydrate and Crataegus fruits extract, for the first time. The influence of capping agents including sucrose, glucose, PVA and reducing agents such as C. microphylla and C. pentagyna on the morphology, size, purity, photocatalytic and antibacterial behavior of magnetic nanocomposites were investigated. The FT-IR, XRD, VSM, EDS, FE-SEM, TEM and BET analysis were performed to confirm the formation of magnetic nanocomposites. MnFe@Si@Au nanocomposites have shown promising potential in degradation of organic contaminants including rhodamine b (RhB), 2-naphthol (2-NPH), methyl violet (MV), erythrosine (ER) and eriochrome black T (EBT) under both radiation conditions. The results show that degradation of the anionic contaminants is more than cationic contaminants under UV and visible irradiations. As well as, these synthesized spherical MnFe@Si@Au nanocomposites show excellent antibacterial activities against P. aeruginosa, K. pneumoniae and P. mirabilis bacteria. In addition to the features mentioned, another prominent feature of this nanocatalyst is retaining their photocatalytic activity after five cycles of utilization.     

Stability analysis and approximate solution of SIR epidemic model with Crowley-Martin type functional response and Holling type-II treatment rate by using homotopy analysis method

In this paper, SIR epidemic model with Crowley-Martin type functional response and Holling type-II treatment rate is investigated. The analysis of the model shows that it has two equilibria, namely disease-free and endemic. We investigate the existence and stability results of equilibria by using LaSalle''s invariant principle and Lyapunov function. $\mathfrak{R}_{0}$ has been found to ensure the extinction or persistence of the infection. Furthermore, homotopy analysis method is employed to obtain the series solution of the proposed model. By using the homotopy solutions, firstly, several $\hbar$-curves are plotted to demonstrate the regions of convergence, then the residual and square residual errors are obtained for different values of these regions. Secondly, the numerical solutions are presented for various iterations and the absolute error functions are applied to show the accuracy of the applied homotopy analysis method.