Two bis-[1-(aryliminomethyleny)-2-oxy-naphthalen] nickel catalysts for the polymerization of methyl methacrylate

Two bis-(1-arylliminomethylenyl-2-oxy-naphthalen) nickel complexes (aryl = 2-methylphenyl, complex 1; aryl = 2,6-diisoproylphenyl, complex 2) were reacted with alkylaluminium in presence of equimolar PPh₃ and tested as catalysts in methyl methacrylate (MMA) polymerization. The two nickel catalysts can initiate polymerization of MMA with good to high activity, the highest activity reaching 1.1 × 10⁵ g PMMA/(mol Ni · h) by less bulky complex 1 at 0.8 mol/L of MMA, 400 of Al/Ni ratio and 0 °C. In addition, the structures of nickel complexes and polymerization conditions, such as monomer concentration, polymerization temperature and Al/Ni molar ratio on catalytic activity of polymerization have great influences on catalytic activity and product properties.     

High-efficiency solution processable electrophosphorescent iridium complexes bearing polyphenylphenyl dendron ligands

We report the synthesis and electrophosphorescent behavior of a series of novel iridium complex materials (Complexes A–F), which are composed of ligands bearing polyphenylphenyl dendron groups and acetylacetonate. Yellow to saturated red organic light-emitting diodes (OLEDs) based on these newly developed Ir complexes were fabricated through solution process by doping the complex materials into polyvinyl carbazole (PVK)/2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (PBD) matrices. The emission wavelengths of the materials could be effectively tuned from 549 nm to 640 nm by changing the conjugation of the ligands either through incorporating additional aromatic segment (e.g. phenyl or fluorenyl group) onto the basic dendron ligand or fusing two of the phenyl rings on the polyphenylphenyl dendron group. High performance devices with the configuration of ITO/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS) (50 nm)/PVK:PBD (40%):Ir complex (6%) (70 nm)/2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) (12 nm)/Alq₃ (20 nm)/Mg:Ag (150 nm) have been demonstrated. For example, when Complex B was used as the emissive layer, maximum current efficiency of 34.0 cd/A and external quantum efficiency of 10.3% have been achieved. When 1,3,5-tris(N-phenylbenzimidazol-2-yl) benzene (TPBI) was used as the block layer, the efficiencies can be further improved to 46.3 cd/A and 13.9%, respectively. These solution processed OLED devices demonstrated quite stable EL efficiencies over a large range of current density, which indicated that triplet–triplet annihilation in electrophosphorescence could be effectively suppressed by incorporation of the polyphenylphenyl dendron structure into iridium complexes.     

火花直读光谱法对铝合金中各元素含量测量结果的不确定度评定

分析了火花直读光谱法测定铝合金中Si、Fe、Cu、Mg、Mn、Zn、Cr、Ti元素含量测量结果的不确定度来源,对不确定度分量进行了评定与计算,Si、Fe、Cu、Mg、Mn、Zn、Cr、Ti测量结果的相对扩展不确定度分别为2. 9%、2. 5%、2. 6%、2. 7%、2. 6%、2. 6%、2. 5%、2. 7%(包含因子k均为2).     

Effects of hydroxyl radicals and oxygen species on the 4-chlorophenol degradation by photoelectrocatalytic reactions with TiO2-film electrodes

The supported nano-TiO₂ electrode was prepared by sol–gel and hydrothermal method, and the photoelectrocatalytic degradation of 4-chlorophenol (4-CP) under UV irradiation has been investigated to reveal the roles of hydroxyl radicals and dissolved oxygen species for TiO₂-assisted photocatalytic reactions. The degradation kinetics, the formation and decay of intermediates, the isotopic tracer experiments with H₂O¹⁸, the removal yield of total organic carbon and the formation of active radical species in the presence of oxygen or not were examined by HPLC, GC–MS, TOC and spin-trap ESR spectrometry. It was found that most of OH radicals in the primary hydroxylated intermediates derived from the oxidation of adsorbed H₂O or HO⁻ by photo-holes in the electrochemically assisted TiO₂ photocatalytic system. It also indicates that the enhancement in the separation efficiency of photogenerated charges by applying a positive bias (+0.5 V vs SCE) has little role in the following decomposition and mineralization of these hydroxylated intermediates in the absence of oxygen. According to above experimental results, the pathway of 4-CP photocatalytic degradation was deduced initially. Due to the combined effect of OH radicals and dissolved oxygen species, the hydroxylated 4-chlorphenol, via cis, cis-3-chloromuconic acid, was decomposed into low molecular weight acid and CO₂.     

Solution‐Based Evolution and Enhanced Methanol Oxidation Activity of Monodisperse Platinum–Copper Nanocubes

Shape‐controlled catalysis : High‐quality Pt–Cu nanocubes with an average size of about 8 nm (see picture, scale bar=20 nm) were synthesized from a high‐temperature organic solution system in the presence of various capping ligands. These cubic Pt–Cu nanocrystals terminated with {100} facets demonstrated a superior catalytic activity towards methanol oxidation compared to similar sized Pt–Cu and Pt nanospheres.

     

A Bahri–Lions theorem revisited

In 1988, A. Bahri and P.L. Lions [A. Bahri, P.L. Lions, Morse-index of some min–max critical points. I. Application to multiplicity results, Comm. Pure Appl. Math. 41 (1988) 1027–1037] studied the following elliptic problem:

where Ω is a bounded smooth domain of , 2<p<(2N−2)/(N−2) and f(x,u) is not assumed to be odd in u. They proved the existence of infinitely many solutions under an appropriate growth restriction on f. In the present paper, we improve this result by showing that under the same growth assumption on f the problem admits in fact infinitely many sign-changing solutions. In addition we derive an estimate on the number of their nodal domains. We also deal with the corresponding fourth order equation Δ²u=|u|^p−2u+f(x,u) with both Dirichlet and Navier boundary conditions, as well as with strongly coupled elliptic systems.     

Corrigendum to: “Oscillation criteria for first-order impulsive differential equations with positive and negative coefficients” [J. Comput. Appl. Math. 217 (1) (2008) 28–37]

This communication gives the corrigendum to the paper “Oscillation criteria for first-order impulsive differential equations with positive and negative coefficients” (JCAM (2007), doi:10.1016/j.cam.2007.06.016).     

Analysis of linear and quadratic simplicial finite volume methods for elliptic equations

This paper is devoted to analysis of some convergent properties of both linear and quadratic simplicial finite volume methods (FVMs) for elliptic equations. For linear FVM on domains in any dimensions, the inf-sup condition is established in a simple fashion. It is also proved that the solution of a linear FVM is super-close to that of a relevant finite element method (FEM). As a result, some a posterior error estimates and also algebraic solvers for FEM are extended to FVM. For quadratic FVM on domains in two dimensions, the inf-sup condition is established under some weak condition on the grid.     

粉末注射成形坯孔隙度的分形模型

粉末注射成形坯是一种具有分形特性的典型的多孔介质,借助于多孔介质孔隙结构的分形理论,对粉末注射成形坯孔隙率的分形模型进行推导。首先分析了粉末注射成形坯孔隙结构的双重分形特性,介绍了粉末注射成形坯孔隙分布分形维数和孔隙迂曲分形维数,然后推导出粉末注射成形坯孔隙度的分形模型。     

Gold(I) eta2-arene complexes

The reaction of 9-{[N-n-propyl-N-(diphenylphosphino)amino]methyl}anthracene (1) with Au(SMe2)Cl yields complex 2 with an arm-opening configuration. The latter is treated with AgClO4 to form complex 4 and then respectively reacted with acetonitrile, pyridine, and triphenylphosphine sulfide to afford novel gold(I) eta2-arene complexes 3a-c, which have arm-closing configurations and feeble or weak fluorescence emissions. The observation can be attributed to charge transfer from the anthracene unit to the Au+ ion. When the solution of 3a or 4 in CH2Cl2 was added with 1 equiv of Ph3P, complex 5 with the arm-opening configuration was formed and strong emission was restored.