Control of selectivity in the generation and reactions of oxonium ylides

Dirhodium catalyzed reactions of aryl-substituted tetrahydropyranone diazoacetoacetates produce ylide intermediates that unexpectedly yield two oxabicyclo[4.2.1]-nonane diastereoisomers, but a single diastereoisomer is formed by increasing the steric bulk of the aryl substituent.     

Selective and sensitive optical chemosensor for detection of Ag(I) ions based on 2(4-hydroxy pent-3-en-2-ylideneamine) phenol in aqueous samples

A selective and sensitive chemosensor, based on the 2(4-hydroxy pent-3-en-2-ylideneamine) phenol (HPYAP) as chromophore, has been developed for colorimetric and visual detection of Ag(I) ions. HPYAP shows a considerable chromogenic behavior toward Ag(I) ions by changing the color of the solution from pale-yellow to very chromatic-yellow, which can be easily detected with the naked-eye. The chemosensor exhibited selective absorbance enhancement to Ag(I) ions in water samples over other metal ions at 438 nm, with a linear range of 0.4–500 μM (r² = 0.999) and a limit of detection 0.07 μM of Ag(I) ions with UV–vis spectrophotometer detection. The relative standard deviation (RSD) for 100 μM Ag(I) ions was 2.05% (n = 7). The proposed method was applied for the determination Ag(I) ions in water and waste water samples.     

Two-dimensional elastic phase-field simulation of fcc to bcc martensitic phase transformations in polycrystals

Numerical results of two-dimensional elastic phase-field simulations of martensitic phase transformations (fcc-bcc) in polycystals are presented. The stresses and strains in the diffuse interface domain are described by following Khachaturyan's approach of microelasticity. A fixed-point iteration algorithm in Fourier space is used to solve the mechanical equilibrium condition for the microscopic, inhomogeneous strain field and apply mechanical loadings to the system. (© 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)     

Crystal Growth of Diazabicyclo[2.2.2]octane-1,4-diium dichromate

Abstract  

The crystal growth of (C₆H₁₄N₂)[Cr₂O₇], consists of a diazabicyclo[2.2.2]octane-1,4-diium cation and a discrete dichromate anion, in solution has been determined under the influence of various factors. Four factors, which influence the crystal size, crystal growth and nucleation, were chosen. These factors are concentration, temperature, type of solvent and method of crystallization. Taguchi design of experiments (DOE) method has been used for to plan a minimum number of experiments and optimization of crystallization processes. Crystallization of diazabicyclo[2.2.2]octane-1,4-diium dichromate with desirable particle size, shape and minimum time of crystal growth as performance characteristics were studied. The changes in the crystal growth habit were observed and could be explained by the differences in the morphology on the various photograph of this compound.     

Stochastic invariance of closed sets with non-Lipschitz coefficients

This paper provides a new characterization of the stochastic invariance of a closed subset of ${\mathbb{R}}^d$ with respect to a diffusion. We extend the well-known inward pointing Stratonovich drift condition to the case where the diffusion matrix can fail to be differentiable: we only assume that the covariance matrix is. In particular, our result can be applied to construct affine and polynomial diffusions on any arbitrary closed set.     

Synthesis of diethyl 2-(aryl)vinylphosphonates by the Heck reaction catalysed by well-defined palladium complexes

Pd-catalysed procedures for the direct Heck arylation of diethyl vinylphosphonate with various aryl or heteroaryl halides toward the synthesis of diethyl 2-(aryl)vinylphosphonates are reported. Several homogeneous catalytic systems (i.e. Herrmann palladacycle, Nolan (NHC)-palladium catalyst, Pd(OAc)₂/PPh₃) were used and compared within the study. High conversions and selectivities were achieved under optimised conditions (2 mol% [Pd], NMP, K₂CO₃, 140 °C) whatever the homogeneous catalyst used.     

Formation of polymeric chain assemblies of transition metal complexes with a multidentate Schiff-base

The new multidentate Schiff-base (E)-6,6′-((1E,1′E)-(ethane-1,2-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-ylidene))bis(4-methyl-2-((E)(pyridine-2-ylmethylimino)methyl)phenol) H₂L and its polymeric binuclear metal complexes with Cr(III), Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Hg(II) are reported. The reaction of 2,6-diformyl-4-methyl-phenol with ethylenediamine in mole ratios of 2:1 gave the precursor 3,3′-(1E,1′E)-(ethane-1,2-diylbis(azan-1-yl-1ylidene))bis(methan-1-yl-1-ylidene)bis(2-hydroxy-5-methylbenzaldehyde) W. Condensation of the precursor with 2-(amino-methyl)pyridine in mole ratios of 1:2 gave the new N₆O₂ multidentate Schiff-base ligand H₂L. Upon complex formation, the ligand behaves as a dibasic octadentate species with the involvement of the nitrogen atoms of the pyridine groups in coordination for all complexes. The mode of bonding and overall geometry of the complexes were determined through physico-chemical and spectroscopic methods. These studies revealed octahedral geometries for Cr(III), Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Cd(II) and Hg(II) complexes of general formulae [Cr₂^III(L)Cl₂]Cl₂, [Ni₂^II(L)(H₂O)₂]Cl₂ and [M₂(L)Cl₂] and five co-ordinate Zn(II) complex of general formula [Zn₂^II(L)]Cl₂.