基于微机电系统光栅平动式光调制器实验和优化设计

基于微机电系统(MEMS)的光栅平动式光调制器(光栅平动式光调制器)调制性能的实验研究关系到其进一步应用。设计了光栅平动式光调制器的相干光学信息处理系统实验方案,He-Ne激光器出射的光束经扩束器和准直透射后成为平行光入射光栅平动式光调制器,被测光栅平动式光调制器放置在相干光学信息处理系统的输入面,滤波器在频谱面上,显微镜放大像面上的信号,经CCD在计算机上记录存储;实验结果和理论分析吻合。对光栅平动式光调制器进行方案优化,将可动光栅边框和悬臂梁表面处理成不反光,使可动光栅和下反射镜构成的整个反射面为光栅周期的整数倍。经理论计算,在光栅周期为8μm,光栅占空比为0.5,光栅边距为2μm,周期数为6的条件下,光栅平动式光调制器图像填充率为74.67%,光学效率为81.06%,衬比度大于5000∶1。     

不同粒径纳米晶硫化锌的高压结构相变研究

 应用原位能量色散X射线散射和金刚石对顶砧技术,对纳米晶ZnS进行了高压结构相变研究。初始相为纤锌矿结构的10 nm和3 nm硫化锌分别在16.0 GPa和16.7 GPa时转变为岩盐矿结构,相变压力均高于纤锌矿结构的体材料硫化锌。该相变为一可逆的结构相变。应用大型科学计算软件Materials Studio（MS）计算了纳米晶ZnS的状态方程,根据Birch-Murnaghan方程拟合了纳米晶ZnS的零压体模量,得到的零压体模量高于相应体材料的零压体模量,表明纳米晶ZnS较难压缩。     

YJ-3000t型紧装式六面顶大腔体高温高压实验装置样品室的压力标定

 在温度为389~1 245 ℃和砧面压力为1.0~5.0 GPa的条件下,利用金属高压熔融标定法,采用Cu、Al、Zn和Pb四种金属,对YJ-3000t型紧装式六面顶大腔体高温高压实验装置样品室内的实际压力进行了标定。通过对由四种金属所获得的标定结果的多项式三维模拟,获得了以叶蜡石为外传压介质、氧化铝为内传压介质的情况下,由砧面压力和样品室温度估算样品室内实际压力的定量表达式。该结果可为今后该设备上类似实验组装中样品腔内实际压力的估算提供方便准确的压力标。     

Organic Nanocrystals Based on a Solid-emission-tunable AIEgen for Cell Imaging

The development of fluorescent nanocrystals based on organic small molecules is of great importance in bioimaging due to the merits of easy modification,high brightness and excellent photostability,however suffering from the emission-detrimental aggregation-caused quenching(ACQ)effect.Herein,we successfully designed and synthesized an AIE-active di(N,N-dimethylaniline)-dibenzofulvene(named as NFTPE),which exhibits the crystallization-induced emission enhancement(CIEE)effect.Interestingly,two types of yellow-and orange-emissive crystals for NFTPE were obtained,exhibiting aggregation microenvironment-dependent emission tuning in the solid state.Single-crystal analysis and density functional theory(DFT)calculations reveal that different aggregation microenvironments result in the distinct molecular conformation for various emission.Excitingly,the crystallization of NFTPE in an aqueous solution under the assistance of amphiphilic PEG polymer matrices could be monitored in situ by the fluorescence changes,facilitating the preparation of NFTPE nanocrystals(NFTPE-NCs)by adjusting the aggregation microenvironment.The obtained NFTPE-NCs exhibit the superior performance in cell imaging in respect to high brightness,photostability,and biocompatibility,thus demonstrating the potential in bioimaging applications.     

DFT insight into asymmetric alkyl–alkyl bond formation via nickel-catalysed enantioconvergent reductive coupling of racemic electrophiles with olefins

A DFT study has been conducted to understand the asymmetric alkyl–alkyl bond formation through nickel-catalysed reductive coupling of racemic alkyl bromide with olefin in the presence of hydrosilane and K₃PO₄. The key findings of the study include: (i) under the reductive experimental conditions, the Ni(ii) precursor is easily activated/reduced to Ni(0) species which can serve as an active species to start a Ni(0)/Ni(ii) catalytic cycle. (ii) Alternatively, the reaction may proceed via a Ni(i)/Ni(ii)/Ni(iii) catalytic cycle starting with a Ni(i) species such as Ni(i)–Br. The generation of a Ni(i) active species via comproportionation of Ni(ii) and Ni(0) species is highly unlikely, because the necessary Ni(0) species is strongly stabilized by olefin. Alternatively, a cage effect enabled generation of a Ni(i) active catalyst from the Ni(ii) species involved in the Ni(0)/Ni(ii) cycle was proposed to be a viable mechanism. (iii) In both catalytic cycles, K₃PO₄ greatly facilitates the hydrosilane hydride transfer for reducing olefin to an alkyl coupling partner. The reduction proceeds by converting a Ni–Br bond to a Ni–H bond via hydrosilane hydride transfer to a Ni–alkyl bond via olefin insertion. On the basis of two catalytic cycles, the origins for enantioconvergence and enantioselectivity control were discussed.

The enantioconvergent alkyl–alkyl coupling involves two competitive catalytic cycles with nickel(0) and nickel(i) active catalysts, respectively. K₃PO₄ plays a crucial role to enable the hydride transfer from hydrosilane to nickel–bromine species.     

Acceptorless dehydrogenative synthesis of primary amides from alcohols and ammonia

The highly desirable synthesis of the widely-used primary amides directly from alcohols and ammonia via acceptorless dehydrogenative coupling represents a clean, atom-economical, sustainable process. Nevertheless, such a reaction has not been previously reported, and the existing catalytic systems instead generate other N-containing products, e.g., amines, imines and nitriles. Herein, we demonstrate an efficient and selective ruthenium-catalyzed synthesis of primary amides from alcohols and ammonia gas, accompanied by H₂ liberation. Various aliphatic and aromatic primary amides were synthesized in high yields, with no observable N-containing byproducts. The selectivity of this system toward primary amide formation is rationalized through density functional theory (DFT) calculations, which show that dehydrogenation of the hemiaminal intermediate into primary amide is energetically favored over its dehydration into imine.

An efficient and selective synthesis of primary amides from alcohols and ammonia, with H₂ evolution, has been achieved by an unprecedented acceptorless dehydrogenative process catalyzed by a pyridine-based PNN–ruthenium pincer complex.     

氢化物发生-原子荧光法测定中药中痕量砷

应用AFS-2202a型双道原子荧光分光光度计,采用高压溶样的消解方式,在选定的仪器工作条件下,建立了氢化物发生-原子荧光测定中药中痕量砷的测定方法。同时,研究了硼氢化钾浓度,光电管负高压,灯电流,载气流量,屏蔽气流量等因素对测定结果的影响。在选定实验条件下,以工作曲线法测定了三种中药样品中痕量砷含量,国家标准物质桃叶(GBW08501)验证结果与推荐值一致。砷的工作曲线在0～80.0 μg·L-1范围内线性良好,线性回归方程为I_f=8.99×c-1.16, 相关系数为0.999 9,检出限为0.069 μg·L-1。     

非线性自回归序列L1估计的渐近分布

由于时间序列数据中经常出现的厚尾特征使得通常的估计方法不再具有渐近的正态分布,在误差项二阶矩有限的条件下考虑了非线性自回归序列的L_1估计.采用局部线性近似的方法得到了具有凸样本路径的随机过程,在此基础上利用凸样本路径随机过程弱收敛的性质证明了非线性自回归序列L_1估计的渐近正态性及无偏性.     

自全国各地100多位理事Road Machinery Branch of China Highway and Transportation Society He

In this paper, a three dimensional ratio-dependent chemostat model with periodically pulsed input is considered. By using the discrete dynamical system determined by the stroboscopic map and Floquet theorem, an exact periodic solution with positive concentrations of substrate and predator in the absence of prey is obtained. When β is less than some critical value the boundary periodic solution (xs(t), 0, zs(t)) is locally stable, and when β is larger than the critical value there are periodic oscillations in substrate, prey and predator. Increasing the impulsive period τ, the system undergoes a series of period-doubling bifurcation leading to chaos, which implies that the dynamical behaviors of the periodically pulsed ratio-dependent predator-prey ecosystem are very complex.