糖尿病大鼠微量元素与动脉血栓形成的关系

为研究糖尿病大鼠微量元素的含量变化及其与动脉血栓形成的关系,用链脲佐菌素（STZ）诱导出糖尿病大鼠模型,三氯化铁（FeCl3）造颈总动脉血栓后,测定血糖、胰岛素（INS）、6-酮-前列腺素F1α（6-K-PGF1α）、血栓素B2（TXB2）、内皮素（ET1）以及全血微量元素镁、锌含量。结果表明,①与正常对照组比,糖尿病大鼠的血糖、TXB2、ET1和锌的含量、ρ（TXB2）／ρ（6-K-PGF1α）、（T／P）比值及血栓质量增加（P〈0．05）,INS含量降低（P〈0．001）,镁和6-K-PGF1α含量无改变（P〉0．05）;②糖尿病组的TXB2与糖、锌（P=0．001）、胰岛素正相关（P=0．003）,ET1仅与锌正相关（P=0．096）,6-K-PGF1α与镁、锌无相关关系。提示：①糖尿病大鼠血管内皮功能受损,血液处于T／P失衡的高凝状态,更易形成动脉血栓;②糖和锌代谢紊乱在T／P失衡和内皮功能损伤中有重要作用。     

Insulator-Metal Transition due to La Doping in Double Perovskite Sr2MnMoO6

Resistivity, thermal diffusivity, lattice and magnetic properties of double perovskite Sr2-xLaxMnMoO6 are investigated with systematic change of La doping concentration x from 0.0 to 0.4. The insulator to metal phase transition is observed with increasing x above 0.3, suggesting that the extra electrons via substitution of La^3 for Sr^2 ions occupy mainly the conduction Mo-4d band. According to the insulator to metal phase transition, the thermal diffusivity of Sr2-xLaxMnMoO6 enhances from 0.33cm^2/s at x=0.0 to 0.49cm^2/s at x=0.4. We further investigate the La doping effects on the lattice and magnetic properties.     

Converting gem-dimethyl groups into cyclopropanes via Pd-catalyzed sequential C-H activation and radical cyclization

A novel route to the synthesis of cyclopropane derivatives is described. 1,1-Dimethyls in 2-(1,1-dimethylalkyl)dimethyloxazolines are first converted into 1,3-diiodide derivatives via Pd-catalyzed sequential C-H activation and then radically cyclized to provide 2-(1-alkylcylclopropyl)dimethyloxazolines. The use of EtOAc as a solvent is crucial for the diiodination of the functionalized substrates. [reaction: see text]     

Pd(II)-catalyzed cross-coupling of sp3 C-H Bonds with sp2 and sp3 boronic acids using air as the oxidant

O-Methyl hydroxamic acids, readily available from carboxylic acids, are found to be extremely reactive for beta-C-H activation by Pd(OAc)2. This reactivity is exploited to develop the first example of cross-coupling sp3 C-H bonds with sp3 boronic acids. Air was shown to be a suitable stoichiometric oxidant for the catalytic oxidative coupling reaction. A biologically active natural product is readily converted to its novel analogues through this coupling reaction.     

Superspreading driven by Marangoni flow

The spontaneous spreading (called superspreading) of aqueous trisiloxane ethoxylate surfactant solutions on hydrophobic solid surfaces is a fascinating phenomenon with several practical applications. For example, the ability of trisiloxane ethoxylate surfactants to enhance the spreading of spray solutions on waxy weed leaf surfaces, such as velvetleaf (Abutilion theophrasti), makes them excellent wetting agents for herbicide applications. The superspreading ability of silicone surfactants has been known for decades, but its mechanism is still not well understood. In this paper, we suggest that the spreading of trisiloxane ethoxylates is controlled by a surface tension gradient, which forms when a drop of surfactant solution is placed on a solid surface. The proposed model suggests that, as the spreading front stretches, the surface tension increases (the surfactant concentration becomes lower) at the front relative to the top of the droplet, thereby establishing a dynamic surface tension gradient. The driving force for spreading is due to the Marangoni effect, and our experiments showed that the higher the gradient, the faster the spreading. A simple model describing the phenomenon of superspreading is presented. We also suggest that the superspreading behavior of trisiloxane ethoxylates is a consequence of the molecular configuration at the air/water surface (i.e. small and compact hydrophobic part), as shown by molecular dynamics modeling. We also found that the aggregates and vesicles formed in trisiloxane solutions do not initiate the spreading process and therefore these structures are not a requirement for the superspreading process.     

Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes

Systematic ligand development has led to the identification of novel mono-N-protected amino acid ligands for Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes. A diverse range of organoboron reagents can be used as coupling partners, and the reaction proceeds under mild conditions. These results provide a new retrosynthetic disconnection for the construction of enantioenriched cis-substituted cyclopropanecarboxylic acids.     

利用光差分技术检测激光激发声表面波定征薄膜材料

利用激光激发声表面波及改进的光差分检测技术,研究沉积在基片表面的薄膜样品的特性和参量。根据实验获得的声色散曲线和基片已知参数,结合层状媒质中声表面波传播理论,拟合得到薄膜材料的弹性模量、密度和厚度等物理量。结合扫描电子显微镜和X光衍射结果分析,并与文献值比较,表明所采用的技术是定征薄膜材料的弹性模量和力学参量的有效方法。     

Pd(II)-catalyzed ortho trifluoromethylation of arenes and insights into the coordination mode of acidic amide directing groups

A Pd(II)-catalyzed trifluoromethylation of ortho C-H bonds with an array of N-arylbenzamides derived from benzoic acids is reported. N-Methylformamide has been identified as a crucial promoter of C-CF(3) bond formation from the Pd center. X-ray characterization of the C-H insertion intermediate has revealed a rare coordination mode of acidic amides as directing groups and the origin of their capacity in directing C-H activation.