长期事件研究方法论——一个综述

本文对国外长期事件研究方法论文献进行了全面的梳理,并着重介绍和分析了期望收益模型(或收益基准)选择、异常收益度量,以及检验统计量的设定与检验力等。研究发现,在各期望收益模型、两种度量异常收益方法—AAR(或CAR)与BHAR的选择,以及各检验统计量是否存在错误设定等问题上,国外学界并未达成共识,争论仍在继续。     

部分相干光在大气湍流中斜程传输路径上的展宽与漂移

基于Andrews和Philips经典漂移方差模型,利用部分相干高斯-谢尔光束在大气湍流中斜程传输的光束扩展半径,推导出考虑外尺度情况时部分相干高斯-谢尔光束斜程情况下的漂移方差表达式,应用随高度变化的大气结构常量模型进行数值计算,对比分析了部分相干光和完全相干光在大气湍流中的展宽和漂移特性.结果表明:相同的传输条件下,部分相干光比完全相干光的光束扩展更迅速,受湍流的影响也更小;初始半径越大,接收机高度越高,光束的扩展效应越小;随着传输距离的增大,光束的质心漂移方差随光束初始半径的增大而减小,不同相干性的光束漂移方差变化很小;完全相干光的光束漂移受波长的影响较小,而部分相干光的波长越长,漂移越明显.     

磁性靶向药物递送中铁磁流体的动力学建模

在所有人体内进行的药物递送技术中,磁性药物靶向递送治疗由于其非入侵性和高靶向性而成为主要的方法．磁性药物靶向递送是将药物装载到磁性纳米颗粒上,利用外部磁场使其移动并聚焦在靶部位的方法．该法能提高靶部位药物的浓度,降低药物对正常组织的毒副作用．尽管已经有不少磁性靶向药物递送的理论分析,但是很少有人研究磁流体在血管里的流体动力学模型．该文提出了一个数学模型来描述作为药物载体的铁磁流体在外磁场作用下,在血管里的流体动力学特性,并在模型中增加了磁场力以及由此产生的不对称应力,增加了磁性纳米颗粒在磁场作用下的角动量方程．由于运动方程的数学复杂性,通过保留数学模型里物理特性最显著项来获得工程近似．用计算流体力学（CFD）进行数值仿真,分析了铁磁流体在一个模拟动脉瘤血管的三维管道里的流动状况,来进一步理解铁磁流体的临床应用．仿真结果和动物实验相一致．分析结果对于磁性靶向药物递送的各种应用提供了可参考的数据．     

无富集进样原子荧光光谱法测定地表水中的痕量汞

通过增大样品进样量的方式,样品进样量是标准进样量的10-100倍,降低了汞的检出限,从而达到了无富集直接进样测定地表水中痕量汞.其检出限为0.008μg/L;浓度为0.05μg/L和0.10μg/L左右的有证标准物质测定均值分别为0.0483μg/L和0.1016μg/L,加标回收率为92.3％和95.2％.灵敏度高,精密度好,能达到准确定量Ⅰ类和Ⅱ类地表水汞(0.05μg/L以下)的要求.对汉江湖北段水样进行测定,在较洁净的地表水分析中,氧化还原处理后与酸化水样测定结果差异不大,处理后水样结果略微增大.建议对较洁净的地表水样品将氧化还原预处理步骤省略掉,直接进样.     

In vivo Toxicity Evaluation of a Nano-drug Delivery System Using a Caenorhabditis elegansModel System

Drug carrier materials need to possess good biological safety. Presently, most biosafety evaluation studies use rodent animal models, including rats and rabbits. However, the cost of raising these animals is relatively high and the experimental period is long. Caenorhabditis elegans(C. elegans) presents an ideal toxicological evaluation model due to its simple structure, easy cultivation, short life cycle, and evolutionary conservation. In this paper, we used C. elegans to test the biological safety of our pH-responsive carrier system(FFPFF self-assembling into a nanosphere structure, FFPFF Nps), which was designed for anti-tumor drug delivery. Our results showed that exposure to high doses of FFPFF Nps did not have a significant impact on the survival rate, growth, development, movement, and reproduction of C. elegans. The preliminary evaluation of the overall biological model of C. elegans shows that FFPFF Nps has good biological safety and warrants further study.     

Heterometallic 3d–4f coordination polymers: Synthesis,characterization and magnetic properties of 1D zigzag chains containing samarium and terbium

Reaction of the copper precursor [Cu(MeOsaltn)(H₂O)] (H₂MeOsaltn = N,N′-bis(3-methoxysalicylidene)-1,3-diaminopropane) with Ln(NO₃)₃·6H₂O (Ln = Sm and Tb) and pyrazine-2,3-dicarboxylic acid (H₂pyrdic) results in the formation of 1D zigzag chains with the general formula of [Cu(MeOsaltn)Ln(NO₃)(pyrdic)]_n·nDMF. X-ray crystal structures reveal that the samarium and terbium compounds are isostructural and crystalize in the orthorhombic space group Pbcn. The chains are composed of heterodinuclear copper–lanthanide building blocks which are linked by the pyrazine-2,3-dicarboxylate bridging units. Temperature-dependent susceptibility measurements indicate antiferromagnetic exchange interactions for the samarium–copper chain whereas for the terbium–copper compound ferromagnetic interactions are observed.     

脯氨酸催化的不对称Aldol反应的研究进展

不对称合成是手性药物制备的核心环节,A ldol反应是重要的形成C—C键的反应之一,在全合成中有广泛应用.脯氨酸的两个异构体均价廉易得,作为一个非金属不对称催化试剂,它催化的不对称A ldol反应立体选择性高,有很好的应用前景.本文就近二十年来脯氨酸催化A ldol反应的机理,溶剂效应,最新进展三方面进行了介绍.     

油茶果壳活性炭的制备及其对Cr(Ⅵ)的去除

利用磷酸活化法制备油茶果壳活性炭,并将其作为吸附剂用于去除水溶液中的Cr(Ⅵ),同时探讨了不同参数(Cr(Ⅵ)的初始浓度、吸附剂的用量、pH、温度等)对油茶果壳活性炭吸附Cr(Ⅵ)的影响。结果表明:当温度为293 K,Cr(Ⅵ)初始浓度为250 mg/L,pH为2.0时,Cr(Ⅵ)的最大吸附量可达165.0 mg/L。根据吸附动力学原理,发现其吸附过程遵循拟二级动力学模型。Cr(Ⅵ)的去除程度随Cr(Ⅵ)初始浓度的升高而增加,且其平衡数据与Freundlich模型拟合良好。     

Kristallstruktur von Na3(NH4)12[Mo57Fe6(NO)6O174(OH)3(H2O)24]·76H2O,einer Verbindung mit einem ungewöhnlichen Clusteranion

Summary The X-ray crystal structure of the compound Na₃(NH₄)₁₂[Mo₅₇Fe₆(NO)₆O₁₇₄(OH)₃(H₂O)₂₄]·76H₂O (3) [P6₃/mmc;a=2380.6(5),c=2763.4(7),Z=2], the giant cluster anion of which has the shape of a doughnut, shows remarkable details: The cluster [{Fe(H₂O)₂}₆{Mo(-H₂O)₂(-OH)Mo}₃{ Mo₁₅(MoNO) ₂ ³⁺ O₅₈(H₂O)₂}₃]^15– can be described as being composed of three transferable {Mo₁₇} ligands bridged by cationic centers and contains a novel nanodimensional central cavity.

     

Chiral tetranuclear mu3-alkoxo-bridged copper(II) complex with 2 + 4 cubane-like Cu4O4 core framework and ferromagnetic ground state

The sugar-modified Schiff base ligand benzyl 2-deoxy-2-salicylideneamino-alpha-D-glucopyranoside H 2L, prepared by condensation of salicylaldehyde and the monomeric chitosan analogue benzyl 2-deoxy-2-amino-alpha-D-glucopyranoside, reacts with copper(II) acetate to form a self-assembled, alkoxo-bridged tetranuclear homoleptic copper(II) complex [{Cu(L)}4] (4) with Cu4O4 heterocubane core. The chiral complex 4 crystallizes in the space group P2 12 12 1. The tetranuclear complex 4 is composed of two dinuclear {Cu(L)}2 entities linked by the four mu 3-bridging C-3 alkoxide oxygen atoms of the sugar backbone. The preorganization of the dimeric {Cu(L)}2 entities is enforced by strong hydrogen bonds between the phenolate oxygen atom and the C-4 hydroxy group of the two constituting chiral monomeric building blocks. Therefore the Cu4O4 core can be classified as a type I or 2 + 4 cubane. The chirality of the structure is confirmed by circular dichroism (CD) spectra, which reveal a significant dichroism associated with the copper centered transitions at around 600 nm. Temperature dependent magnetic susceptibility measurements indicate ferromagnetic exchange interactions in complex 4. Fitting of the experimental data with a two J model based on the 2 + 4 topology ( H = - J1(S1S3 + S2S4) - J2(S1 + S3)(S2 + S4)) leads to exchange coupling constants of J1 = 64 and J2 = 4 cm(-1). The observed ferromagnetic coupling can be attributed to the very small Cu-O-Cu bridging angles within the Cu2O2 core of the constituting dimeric entities, which are a result of the conformational requirements introduced by the sugar backbone. 4 is not only the first example of an alkoxo-bridged tetranuclear copper(II) complex with Cu4O4 core representing the 2 + 4 cubane class with ferromagnetic ground state but also a rare example for the class of molecules combining a ferromagnetic ground state with optical activity. The ferromagnetic S = 2 ground state of 4 is confirmed by magnetization measurements and ESR spectroscopy.