原子力显微术轻敲模式中探针样品接触过程及相位衬度研究

借助简单的有阻尼受迫振子模型，研究了原子力显微术轻敲模式中探针与样品接触时间t_c、样品的表面形变D_z和相位衬度对探针设置高度z_c及样品杨氏模量E_s的依赖关系.结果发现,t_c与D_z均随E_s及z_c的增大而减小，同时探针与样品作用过程伴随很小的能量耗散.对轻敲过程中相移量φ的研究表明，E_s较大的样品有较小的φ，且φ随 关键词： 原子力显微术 轻敲模式 相位衬度     

An effective method for improving diffraction performance of magnetostatic backward volume wave-based magneto-optic Bragg cells by using an appropriately tilted bias magnetic field in YIG film plane

The universal magneto-optic (MO) coupled-mode equations for magnetostatic waves (MSWs) and guided optical waves (GOWs) under arbitrarily tilted bias magnetic fields are presented for the first time and, as an example, applied to the noncollinear Stokes interaction between the incident TE₀-mode light and magnetostatic backward volume wave (MSBVW) excited by single-element microstrip line transducer in yttrium–iron–garnet (YIG) film. Our calculation indicates that, for the case of magnetization parallel to the MSBVW propagation direction, the diffraction efficiency (DE) is equal to the mode-conversion efficiency of the diffracted lights (MCDE) and the calculated curve of relative DE for the MSBVW-based MO Bragg cell in pure YIG waveguide is in good agreement with the experimental data. In contrast, the diffraction performance can be greatly improved by optimizing the bias magnetic field and the DE gain can be increased by 6.3 dB in the tangentially magnetized film. The angular dependences of the DE and the corresponding Bragg angle upon the magnetization direction are also discussed in the paper.     

Vinyl copolymers containing pendant 1,4‐distyrylbenzene and 1,3,4‐oxadiazole chromophores: Preparation and optoelectronic properties

We prepared two vinyl copolymers P1 and P2 containing pendant distyrylbenzene and aromatic 1,3,4‐oxadiazole derivatives, respectively, from their precursor poly(styrene‐ran‐4‐vinylbenzyl chloride) (M_w = 11,400, PDI = 1.18), which had been prepared by the controlled radical polymerization (RAFT). Two main chain polymers containing similar isolated distyrylbenzene ( P3) and aromatic 1,3,4‐oxadiazole ( P4 ) chromophores were also synthesized for comparative study. The resulted copolymers ( P1 – P4 ) are soluble in common organic solvents and are basically amorphous materials with 5% weight‐loss temperature higher than 360 °C. The PL spectral results reveal that the architecture of P1 prevents the formation of inter‐ or intramolecular interaction. The HOMO and LUMO levels of P2 , estimated from cyclic voltammetric data, are ?5.96 and ?3.81 eV, respectively, which are much lower than those of P1 (?5.12 and ?3.11 eV). The emission of blend from P1 and P2 are contributed mainly from distyrylbenzene fluorophore (～450 nm) owing to efficient energy transfer. Moreover, the blend exhibits three kinds of redox behavior depending on their weight ratios. The luminance and current efficiency of the EL device lpar;ITO/PEDOT/ MEH ‐ PPV + P2 /Al) are 503 cd/m² and 0.11 cd/A, which can be improved to 1285 cd/m² and 0.44 cd/A, respectively, as the weight ratio of P2 increases from 0 to 20%. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5362–5377, 2006     

A pair of orthogonal frames

We start with a characterization of a pair of frames to be orthogonal in a shift-invariant space and then give a simple construction of a pair of orthogonal shift-invariant frames. This is applied to obtain a construction of a pair of Gabor orthogonal frames as an example. This is also developed further to obtain constructions of a pair of orthogonal wavelet frames.     

海螵蛸入药部分和废弃部分8种无机元素分析

为合理开发利用海螵蛸 ,用原子吸收分光光度法测定了海螵蛸中入药部分和废弃部分中8种人体必需无机元素含量。结果表明 ,入药部分和废弃部分中钙含量丰富 ,分别达到 742 1 3× 1 0 - 3和 65 9 76× 1 0 - 3。入药部分铜、铁含量较废弃部分高 ,分别为 9 41× 1 0 - 6 、 91 86× 1 0 - 6 和2 3 5× 1 0 - 6 、 2 5 7× 1 0 - 6 。废弃部分含锌丰富 ,为 3 5 3 62× 1 0 - 6 ,数倍于入药部分 64 65× 1 0 - 6 。可见海螵蛸入药部分和废弃部分均具有良好的开发前景     

氨基酸与钠离子非共价键相互作用的电喷雾质谱研究

实验研究中常常观察到钠离子与一些多肽或蛋白质有较强的非共价键结合能力,这种非共价键相互作用可能与生物的一些功能和活性有关。为了进一步了解这一结合作用,我们应用电喷雾质谱研究了常见的20种氨基酸与钠离子在溶液中的非共价键相互作用。实验研究中发现脯氨酸和苯丙胺酸与钠离子有较强的非共价键结合能力。     

3-羟基-6-O-甲基红霉素的合成优化与副产物的分析

分别以甲醇和水为溶剂,探讨了克拉霉素脱克拉定糖反应的主要产物,结果发现:以甲醇为溶剂得到的不是3-羟基-6-O-甲基红霉素,而是3-羟基-8,9,10,11-二脱水-9,12-半缩酮-6-O-甲基红霉素.以水为溶剂得到了3-羟基-6-O-甲基红霉素,收率94.7%.     

4-(N-甲酰基-N′-邻氯苯基硫脲)-N-邻氯苯基苯氧乙酰胺的核磁共振研究

在超声波辐射下,以PEG-400为固-液相转移催化剂,用邻氯苯胺与双酰基异硫氰酸酯反应,合成出了一种新的化合物——4-(N-甲酰基-N′-邻氯苯基硫脲)-N-邻氯苯基苯氧乙酰胺。实验中观察到了取代和加成反应的竞争。利用元素分析,1H、13C、APT及二维核磁共振技术确定了所合成的新化合物的结构。给出了该化合物的化学位移数据。所得的结果对这类化合物的结构解析很有价值。     

催化裂化USY／ZnO／Al2O3脱硫添加剂的高温水热失活

 对USY／ZnO／Al2O3汽油催化裂化脱硫添加剂经高温水热老化处理前后的脱硫性能进行了考察，发现老化后添加剂的脱硫性能大幅度下降．采用XRD和IR等技术对USY／ZnO／Al2O3添加剂在高温和高温水热条件下失活的原因进行了研究．结果表明，在高温下，ZnO可与USY沸石中的铝发生固相反应生成ZnAl2O4尖晶石，从而造成USY晶体结构崩塌，转变成无定形状态．在ZnO含量较高的条件下，ZnO可继续与USY晶体结构崩塌后生成的无定形的硅和铝的氧化物反应，生成Zn2SiO4硅锌矿和ZnAl2O4尖晶石结构．这一方面使添加剂失去了可形成硫化物吸附中心的ZnO，另一方面破坏了硫化物的裂化活性组分USY，从而造成添加剂脱硫性能下降甚至失去脱硫活性．ZnO对USY的破坏作用主要与温度有关．在USY／ZnO／Al2O3体系中，ZnO被ZnO与Al2O3之间形成的锌铝尖晶石膜固定并与USY隔离，单纯的高温条件对添加剂的破坏不显著，而水蒸气可以促进ZnO的移动，有利于ZnO与USY的接触，因此在高温和有水蒸气存 在的条件下添加剂的结构易遭到破坏．     

1‐Acetyl‐3′‐(4‐bromophenyl)‐3′‐chlorospiro[3H‐indole‐3,2′‐oxetan]‐2(1H)‐one

In the title compound, C₁₈H₁₃BrClNO₃, the heterocyclic ring of the indole is distorted from planarity towards an envelope conformation. The orientations of the indole, oxetane, chloro and bromo­phenyl substituents are conditioned by the sp³ states of the spiro‐junction and the Cl‐attached C atoms.