A one-pot reaction of (chlorocarbonyl) phenyl ketene with β-ketoamides and thiochromen-2-one

Readily available (chlorocarbonyl)phenyl ketene and a varied set of β-ketoamides were reacted in a one-step procedure to produce 2-pyrone derivatives. β-Ketoamide derivatives are versatile intermediates for the synthesis of heterocyclic compounds. For instance, 1-morpholino-3-phenyl-1,3-propanedione, 1-phenyl-3-piperidino-1,3-propanedione, 1-phenyl-3-pyrrolidino-1,3-propanedione, 1-piperidino-1,3-butanedione, 1-morpholino-2-phenyl ethanone were used in these reactions to produce 2-pyrone derivatives. In addition, the preparation of 4-hydroxy-3-phenylthiochromeno[4,3-b]pyran-2,5-dione derivatives and 4-hydroxy-7-methyl-3-phenyl pyrano[3,2-c]chromeno-2,5-dione were described. For the synthesis of these compounds 4-hydroxy-2H-thiochromen-2-ones and 4-hydroxy-8-methyl-2H-chromen-2-one were reacted with (chlorocarbonyl)phenyl ketene and the final products were isolated in good yields.     

New Synthesis of Acetaminophen Derivatives Containing a Phosphorus Atom

Two derivatives of acetaminophen have been efficiently prepared from 4-aminophenol via a two-step procedure involving acetylation of OH and NH ₂ groups and then the reaction of the acetylated compounds with diakyl acetylenedicarboxylate in the presence of triphenylphosphine. The products were obtained in good yields.     

Electrical conductivity and dielectric relaxation studies of a polymeric hybrid compound: ([C2H10N2]CdCl2(SCN)2)n

Electrical conductivity and dielectric measurements of ([C₂H₁₀N₂]CdCl₂(SCN)₂)_n were carried out from 200 Hz–5 MHz over a temperature range of 307–352 K. The frequency dependence of electrical data have been analyzed in two frameworks: the electrical modulus formalism with the Kohlrausch-Williams-Watts (KWW) stretched exponential function and the electrical conductivity by using the Jonscher’s power law σ′_Tot(ω,T) = σ_DC(T) + A(T)ω^s(T) in the frequency domain. The conduction mechanism is attributed to the nonoverlapping small polaron tunneling (NSPT) model. Furthermore, the dielectric data have also been analyzed in modulus and polarizability formalisms. The close values of activation energies obtained from the conductivity, the relaxation process, the electric modulus, and the complex polarizability data confirm that the transport is through ion-hopping mechanism.     

On the Origin of Damped Electrochemical Oscillations at Silicon Anodes (Revisited)

Electrochemical oscillations accompanying the formation of anodic silica have been shown in the past to be correlated with rather abrupt changes in the mechanical stress state of the silica film, commonly associated with some kind of fracture or porosification of the oxide. To advance the understanding on the origin of such oscillations in fluoride‐free electrolytes, we have revisited a seminal experiment reported by Lehmann almost two decades ago. We thereby demonstrate that the oscillations are not stress‐induced, and do not originate from a morphological transformation of the oxide in the course of anodisation. Alternatively, the mechanical features accompanying the oscillations can be explained by a partial relaxation of the field‐induced electrostrictive stress. Furthermore, our observations suggest that the oscillation mechanism more likely results from a periodic depolarisation of the anodic silica.     

Direct acylation of aryl bromides with aldehydes by palladium catalysis

A new protocol for the direct acylation of aryl bromides with aldehydes is established. It appears to involve palladium-amine cooperative catalysis, affording synthetically important alkyl aryl ketones in moderate to excellent yields in a straightforward manner, and broadening the scope of metal-catalyzed coupling reactions.     

Analysis of the transverse and the longitudinal pseudodiffusion of CO2 in sub- and supercritical states: a molecular-dynamics analysis

We have performed molecular-dynamics simulations of CO(2) system along the gas-liquid coexistence curve and on the isochore 94.22 cm(3) mol(-1) (which corresponds to the critical isochore). The calculation has been carried out in order to analyze the diffusion of CO(2) and particularly to figure out how the diffusion coefficient may be decomposed along the molecular axes. This makes it possible to analyze the anisotropy of the diffusion along these axes and to shed light on the microscopic changes which accompany such behavior. This anisotropy is traced back to the effect of the translation-rotation coupling (TRC) along the molecular axes. Along the liquid-gas coexistence curve, the pseudolongitudinal diffusion is found to be more rapid than the transverse one. The opposite trend is found along the isochore 94.22 cm(3) mol(-1). The role of the local structure was explored by calculating intermediate scattering function and the autocorrelation functions for the forces acting along the molecular axes. It is shown that the strength of the TRC effect is correlated to the difference between the relaxation times of the local structure, that of the reorientation along the molecular axes, and that of the translational motion. The analysis of the correlation time and the average mean square force along the longitudinal and transverse directions confirms the anisotropy of the local environment that determines the translational dynamics of a molecule.     

Analytical solution for Van der Pol–Duffing oscillators

In this paper, the problem of single-well, double-well and double-hump Van der Pol–Duffing oscillator is studied. Governing equation is solved analytically using a new kind of analytic technique for nonlinear problems namely the “Homotopy Analysis Method” (HAM), for the first time. Present solution gives an expression which can be used in wide range of time for all domain of response. Comparisons of the obtained solutions with numerical results show that this method is effective and convenient for solving this problem. This method is a capable tool for solving this kind of nonlinear problems.