Flat Supercontinuum Generation at 1550 nm in a Dispersion-Flattened Microstructure Fibre Using Picosecond Pulse

The generation of a flat supercontinuum of over 80nm in the 1550nm region by injecting 1.6ps 10 GHz repetition rate optical pulses into an 80-m-long dispersion-flattened microstructure fibre is demonstrated. The fibre has small normal dispersion with a variation smaller than 1.5 （ps·nm^-1·km^-1） between 1500 and 1650nm. The generated supercontinuum ranging from 1513 to 1591 nm has the flatness of ±1.5 dB and it is not so flat in the range of several nanometres around the pump wavelength 1552nm. Numerical simulation is also used to study the effect of optical loss, fibre parameters and pumping conditions on supercontinuum generation in the dispersion-flattened microstructure fibre, and can be used for further optimization to generate flat broad spectra.     

双离子(40Ar+,C2H6+)辐照合成金刚石纳米晶颗粒

用双离子(40Ar+,C1H6+)辐照实验完成了从多壁碳纳米管向金刚石纳米晶颗粒的转变.对转变机理进行了初步探讨.这一探索有望能成为一种金刚石纳米晶合成的新途径.由此可知,多重荷能离子辐照用于其他材料纳米结构的制备也不是凭空设想.     

Theoretical study of stereodynamics for the N+H2/D2/T2 reactions

The effects of isotopic variants on stereodynamic properties for the title reactions have been investigated using a quasi-classical trajectory method based on the first excited state NH2（I^2A＇） potential energy surface [Li Y Q and Varandas A J C 2010 J. Phys. Chem. A 114 9644]. The forward–backward symmetry scattering of the differential cross section can be observed, which demonstrates that all these reactions follow the insertion mechanism. Three angle distribution functions P（θr）, P（φr）, and P（θr, φr） with different collision energies and target molecules H2/D2/T2 are calculated. It is shown that the product rotational angular momentum is not only aligned, but also oriented along the direction perpendicular to the scattering plane. The title reaction is mainly governed by the ＂in-plane＂ mechanism through the calculated distribution function P（θr, φr）. The observable influences on the rotational polarization of the product by the isotopic substitution of H/D/T can be demonstrated.     

十二顶点邻位双取代碳硼烷衍生物二阶NLO性质的理论研究

采用密度泛函理论(DFT) B3LYP/6-31G*方法, 对系列十二顶点邻位双取代碳硼烷(C2B10H12)衍生物的几何构型进行优化. 在所得优化结构的基础上, 结合有限场方法(FF)和含时密度泛函理论(TD-DFT)对这些分子的二阶非线性光学(NLO)活性及电子吸收光谱进行了研究. 结果表明, 邻位双取代碳硼烷有较强的吸电子作用, 与有机基团形成D-π-A结构时, 可以起到很好的受体作用. 当给体部分或桥的共轭性好, 给体的给电子能力强时, 邻位双取代碳硼烷的吸电子作用更明显, 从而增强了分子的二阶NLO响应.     

茄黄斑螟性信息素化学的结构签定(英文)

本文采用TLC、GC、微量臭氧化和GC-MS等分析方法,从茄黄斑螟雌蛾性腺体提取物中,分离和鉴定出性信息素反-11-十六碳烯醇乙酸酯(1a)。触角电位和田间试验证明,天然提取物和合成样品均有强烈的生物活性。     

窄缝中气泡在磁性液体中的上升与变形

对窄缝中气泡在磁性液体中的上升与变形进行了可视化研究。定性分析了纳米磁性颗粒引发的黏度效应及表面活性剂分子依附作用对气泡上升速度与形状的影响。试验工质为体积浓度6.33%的水基Fe_3O_4磁性液体,同时对比了质量浓度25%的四甲基氢氧化铵水溶液、质量分数30%和50%的蔗糖溶液以及水中气泡的上升运动。窄缝间隙分别为1 mm和2 mm,气泡由底部不同直径的圆孔产生。试验结果表明:由于活性剂分子的存在,磁性液体气泡上升过程中由扁椭圆形渐转变为上圆下平的冠状,而其略大于水的黏度使气泡在1 mm窄缝中保持直线上升运动,但窄缝间隙增大到2 mm后,磁性液体中气泡的运动轨迹仍会发生振荡。     

电磁波对化学反应非致热作用的实验研究

微波加快化学反应速度除微波对反应物的加热以外还有非致热的作用，本文用实验证实了电磁波对离子和极性分子的洛仑兹力的作用导致了指前因子和活化能的变化，并提出用电磁作用因子描术电磁波对化学反应作用的大小。     

抗霉素合成概览

抗霉素(antimycin)是一大类具有九元环双内酯的天然抗生素, 最早发现于20世纪40年代末. 在随后的50多年中不断地有新的成员被发现, 到目前为止已多达26个. 这类化合物的结构主要是通过抗霉素A_3b来确定的, 所以合成工作也是围绕该成员展开的. 对文献中已有报道的合成工作加以综述, 对各方法的主要优缺点也进行了简要的分析.     

Direct electrochemistry and electrochemical catalysis of immobilized hemoglobin in an ethanol–water mixture

Hemoglobin (Hb) was immobilized on a glassy carbon electrode (GCE) surface by konjac glucomannan (KGM). KGM hydrogel films on GCE have relatively high stabilities in aqueous–ethanol mixtures. The entrapped hemoglobin undergoes fast direct electron transfer reactions in aqueous–organic solvent mixtures. The peak current is bigger, the peak-to-peak separation smaller and the formal potential observed in the cyclic voltammogram is more negative for Hb–KGM/GCE in ethanol–PBS compared to Hb–KGM/GCE in PBS. The electrochemical properties of the Hb in aqueous–organic solution are almost unchanged from with those observed for the purely aqueous solution, suggesting that water pools in the KGM hydrogel play an important role in preventing changes in conformation and making proteins unreactive with polar organic solvents. The immobilized Hb was able to catalyze the reduction of nitric oxide, peroxides (hydrogen peroxide, cumene hydroperoxide, t-butyl hydroperoxide, 2-butanone peroxide), and the dehalogenation of haloethanes (hexachloroethane, pentachloroethane, tetrachloroethane, etc.). The stability and reproducibility of the modified electrode meant that it could be used to determine these substances.