基于荧光内滤效应的锂离子荧光化学传感器研究

报道了一种基于荧光内滤效应的荧光增强型锂离子光化学传感器,将荧光试剂、亲脂性pH指示剂和锂离子中性载体结合在增塑的PVC膜中,Li⁺与H⁺在膜相中的竞争萃取效应引起受亲脂性pH指示剂调制的敏感膜荧光值的变化.推导了有关理论关系式,研究了该传感器的响应特性,并对人工合成样品进行测试,结果较为满意.     

光束旋转90°多程放大系统的波前误差校正

光束通过神光-Ⅲ原型装置四程放大系统发生了90°旋转和扩束。在四程放大系统腔镜处放置变形镜校正系统像差是一种新的自适应光学方案，推导出被校正像差与变形镜面形之间的数学关系。理论推导表明，在扩束比大于1的前提下，腔镜处变形镜可以校正系统输出的任意类型的像差，且变形镜对应的面形唯一。理论分析和计算仿真说明该方案的校正能力与像差类型和扩束比有关，扩束比增大将增强变形镜校正像散的能力，但系统旋光消像散的能力也将减弱。     

Negative Refraction and Near-Field Imaging of an Elliptical-Rod Photonic Crystal Slab in the Second Band

Negative refraction and imaging properties of the electromagnetic wave through a two-dimensional photonic crystal （PC） slab, which consists of a square lattice of elliptical dielectric rods immersed in the air background, is studied by the plane-wave expansion method and the finite-difference time-domain method. A point source placed in the vicinity of the PC slab can form a good-quality image spot through the PC slab for the incident frequencies within the second photonic band. The calculated result also shows that negative refraction occurs in this kind of PC slab.     

Oxidation kinetics of thin copper films and wetting behaviour of copper and Organic Solderability Preservatives (OSP) with lead-free solder

The oxide formation on thin copper films deposited on Si wafer was studied by XPS, SEM and Sequential Electrochemical Reduction Analysis SERA. The surfaces were oxidized in air with a reflow oven as used in electronic assembly at temperatures of 100 °C, 155 °C, 200 °C, 230 °C and 260 °C. The SERA analyses detected only the formation of Cu₂O but the XPS analysis done for the calibration of the SERA equipment proved also the presence of a CuO layer smaller than 2 nm above the Cu₂O oxide. The oxide growth follows a power-law dependence on time within this temperature range and an activation energy of 33.1 kJ/mol was obtained. The wettability of these surfaces was also determined by measuring the contact angle between solder and copper substrate after the soldering process. A correlation between oxide thickness and wetting angle was established. It was found that the wetting is acceptable only when the oxide thickness is smaller than 16 nm. An activation energy of 27 kJ/mol was acquired for the spreading of lead free solder on oxidized copper surfaces.From wetting tests on copper surfaces protected by Organic Solderability Preservatives (OSP), it was possible to calculate the activation energy for the thermal decomposition of these protective layers.     

水下光通信PPM数字接收机的DSP实现

水下光通信充分利用了海水对激光的衰减窗口效应,具有隐蔽、安全、非接触和快速机动等特性,兼具无线通信和光纤通信的优点,其关键技术在于光收发端机的研制;PPM(Pulse Position Modulation)数字脉冲位置调制具有低平均功率和高峰值功率等特性,特别适合用于无线数字光通信。两者性能的融合需要高灵敏度数字光接收机的实现。利用阵列光电检测接收、高速A/D转换和信号处理等相关技术,采用DSP处理器,高灵敏度的数字光PPM接收机得以实现,实验和测试表明它大大降低了接收机对于整个系统信噪比的要求,获得了较好的性能。     

Multiplexed therapeutic drug monitoring of antipsychotics in dried plasma spots by LC‐MS/MS

In this work, a convenient method for the therapeutic monitoring of seven common antipsychotic drugs in “dried plasma spot” samples has been developed. It is based on the liquid chromatography tandem mass spectrometry technique, operating in multiple reaction monitoring mode, and a straightforward procedure for the simultaneous extraction of all antipsychotics in a single step, with high extraction yield. The method was fully validated with proper accuracy, precision, selectivity and sensitivity, for all the drugs. Limits of quantification were 0.12, 1.09, 1.46, 1.47, 5.70, 1.32, 1.33 µg/L for haloperidol, aripiprazole, olanzapine, quetiapine, clozapine, risperidone, and paliperidone, respectively. Accuracy, intra‐ and interday precision values were <10% for all drugs at all concentration levels examined. The method was tested in the analysis of 30 plasma samples from real patients for each drug. The proposed analytical approach, by combining practical and logistical advantages of microsampling with liquid chromatography tandem mass spectrometry analytical performance, could offer an ideal strategy for accurate and timely therapeutic drug monitoring of antipsychotic drugs in most clinical settings, even in remote centers and/or in out‐patient settings, bringing so many potential improvements in psychiatric patient care.     

共面对称条件下Mg原子(e,2e)反应的三重微分截面的计算

采用修正的扭曲波玻恩近似(DWBA)方法,本文计算了共面对称几何条件下电子碰撞Mg(3s2) 原子(e,2e)反应的三重微分截面.理论方法通过引入Gamow因子来表示(e,2e)反应的后碰撞相互作用(PCI).将计算结果与实验结果及标准DWBA计算结果进行了比较,发现PCI效应起着重要的作用.     

二维流场、热结构松耦合模拟研究

本文针对轴对称型飞行器前缘部位,采用松耦合方法,开展了二维高超声速流固界面的热耦合计算。满足非稳态N-S方程的外部流场和内部非稳态热传导均采用商用软件FLUENT进行计算。通过对相同时刻,不同松耦合推进时间步长引起的壁面热流密度、壁面温度、表面传热系数的差异对比,得出了松耦合推进时间对以上参数的影响规律,这对有效实施松耦合方法进行高超声速飞行器模拟具有积极意义。     

New palladium (II) complexes containing phosphine‐nitrogen ligands and their use as catalysts in aminocarbonylation reaction

Aminocarbonylation of aryl halides, homogeneously catalysed by palladium, is an efficient method that can be employed for obtaining amides for pharmaceutical and synthetic applications. In this work, palladium (II) complexes containing P^N ligands were studied as catalysts in the aminocarbonylation of iodobenzene in the presence of diethylamine. Two types of systems were used: a palladium (II) complex formed in situ; and one prepared prior to the catalytic reaction. In general, the palladium complexes studied achieved high conversions in an average reaction time of less than 2 hr, which is less than that for the standard system (Pd (II)/PPh₃) used. The pre‐synthesized complexes were faster than their in situ counterparts, as the latter require an induction time to form the Pd/P^N species. The structure and electronic properties of the ligand P^N can influence both the activity and the selectivity of the reaction, stabilizing the acyl‐palladium intermediates formed in a better manner.     

First Total Synthesis of Hyacinthacine A6 from the Protected Derivative of Polyhydroxylated Pyrrolidine

（1S、2R、3R、5R、7aR）-1,2-Dihydroxy-3-hydroxy methyl-5-methylpyrrolizidine（hyacinthacine A6, I） was synthesized by Wittig＇s methodology via the reaction of aldehyde 6, prepared from the partially protected derivative of polyhydroxylated pyrrolidine, with appropriated ylides, followed by cyclization through the intemal reductive amination process of the resulting a,B-unsaturated ketone 7, and total deprotection.