Solvent induced different morphologies of bis(propyl)triethoxysilane substituted perylenediimide and their optical properties

Nano/microstructure of bis(propyl)triethoxysilane substituted perylenediimide (1) with nanoparticle and twisted microrod morphologies were obtained by reprecipitation method induced by water and petroleum ether, respectively. It is believed that the different nucleation and growth processes involved are responsible for the formation of the nano/micro-structure With different morphologies of 1. UV-vis absorption and photoluminescence measurements show that their UV-vis absorption and photoluminescence properties are different from each other as well as their monomer mid bulk materials due to the different effects on the change transfer (CT) transition energy levels caused by their different aggregation behaviors.

A wide-bandgap semiconducting polymer for ultraviolet and blue light emitting diodes

A novel wide-bandgap conjugated polymer (PDHFSCHD) consisting of alternating dihexylfluorene and rigidly twisted biphenyl units has been synthesized. The new fluorene-based copolymer composed of rigid twisting segments in the main-chain exhibits an optical bandgap of as high as 3.26 eV, and a highly efficient ultraviolet emission with peaks at 368 nm and 386 nm. An electroluminescence device from PDHFSCHD neat film as an active layer shows UV emission which peaks at 395 nm with a turn on voltage below 8 V By optimizing the device conditions, a peak EL quantum efficiency of 0.054% and brightness of 10 cd.m(-2) was obtained. Furthermore, blending a poly(dihexylfluorene) in the PDHFSCHD host gave pure blue emission peaking at 417 nm, and 440 nm without long wavelength emission from aggregated species. Efficient energy transfer from PDHFSCHD to PDHF was demonstrated in these blended systems. Depressed chain-aggregation of PDHF in the PDHFSCHD host can correspond to pure blue emission behaviors.

Effect of configuration and conformation on the spin multiplicity in xylylene type biradicals

The singlet-triplet splitting energy gap DeltaE(S.T) = E-S - E-T is calculated for the ortho-, meta-, and para-xylylenes and their heteroatomic analogous by means of AM1-CI approach. It is shown that when the radical centers R-.(R-.=H2C.-,H2N.+- or HN.-) are twisted sufficiently Tar out of conjugation with the benzene ring, DeltaE(S.T) tends to zero or is negative, i.e, ortho-, meta-, and para-phenylenes turn into weak ferromagnetic or antiferromagnetic coupling unit, while they are strong ferromagnetic (meta-isomers) or antiferromagnetic (ortho-, para-isomers) coupling units under planar conformation. It is suggested that serious twisted conformation is not recommended candidate for the design of novel high-spin molecules with stable high-spin ground states by ortho- or para-phenylene coupling unit.

Aggregation behavior of amphiphilic D-pi-A molecules bearing recognition group

Aggregation behavior of two amphiphilic D-pi -A molecules bearing barbituric acid as both recogniton group and electron-drawing substituent, 5-(4-dodecyl oxybenzylidene)-(1H, 3H)-2,4,6-pyrimidine trione (PB12) and 5-(4-N,N-didodecyl aminobenzylidene)-(1H,3H)-2,4,6-pyrimidine trione (AB(12)) was studied by UV-visible, fluorescence, and surface voltaic spectroscopies (SPS). The experimental results indicate that PB12 tends to form J-aggregate and AB(12) tends to form H-aggregate under increasing concentration. An intramolecular twisted charge transfer (TICT) emission around 500 nm is observed when J-aggregate is formed between PB12 molecules, and an excimer emission around 600 nm is observed when H-aggregate is formed between AB(12) molecules.

Helical single-lamellar crystals thermotropically formed in a synthetic nonracemic chiral main-chain polyester

Phase structures and transformation mechanisms of nonracemic chiral biological and synthetic polymers are fundamentally important topics in understanding their macroscopic responses in different environments. It has been known for many years that helical structures and morphologies can exist in low-ordered chiral liquid crystalline (LC) phases. However, when the chiral liquid crystals form highly ordered smectic liquid crystal phases, the helical morphology is suppressed due to the crystallization process. A double-twisted morphology has been observed in many liquid crystalline biopolymers such as dinoflaggellate chromosomes (in Prorocentrum micans) in an in vivo arrangement. Helical crystals grown from solution have been reported in the case of Bombyx mori silk fibroin crystals having the beta modification. This study describes a synthetic nonracemic chiral main-chain LC polyester that is able to thermotropically form helical single lamellar crystals. Flat single lamellar crystals can also be observed under the same crystallization condition. Moreover, flat and helical lamellae can coexist in one single lamellar crystal, within which one form can smoothly transform to the other. Both of these crystals possess the same structure, although translational symmetry is broken in the helical crystals. The polymer chain folding direction in both flat and helical lamellar crystals is determined to be identical, and it is always along the long axis of the lamellae. This finding provides an opportunity to study the chirality effect on phase structure, morphology, and transformation in condensed states of chiral materials. [S0163-1829(99)01042-5].

Optical properties of organo-soluble polyimide thin films and their applications in liquid crystal displays

Three organo-soluble polyimide powders have been synthesized. Their imidization was verified by Fourier transform infrared (FTIR) and thermal gravimetric analysis (TGA) techniques. The amorphous morphology of their thin films were confirmed by X-ray diffraction. Polyimide thin films were prepared by solution casting or spin coating. UV-visible transmission spectra of thin films revealed that they are almost transparent in the range of visible light. With in-plane orientation, revealed by FTIR spectra, negative birefringence (Delta n) of thin films were observed, and refractive indices of the thin films along the film plane (n(TE)) and normal to the plane (n(TM)) were measured by a prism coupler. Because of negative birefringence of the thin films, they tan be substituted for the compensation films for twisted nematic liquid crystal displays (TN-LCDs) to extend their viewing angles. In this paper, a 90 degrees C TN-LCD and 120 degrees C TN-LCD were taken as examples to show the compensation effect of thin films of a qualified polyimide. (C) 1998 Elsevier Science S.A. All rights reserved.

Polyimide thin films as compensators for liquid crystal displays

The disadvantages of NW-TN-LCD (normally white twisted nematic liquid crystal display) are discussed. The reason that the negative birefringent polyimide thin films are used to compensate NW-TN-LCD to decrease off-axis leakage, improve contrast ratios and enlarge viewing angeles is explained. A certain polyimide thin film is taken as an example to show the compensation effect on NW-TN-LCD. (C) 1997 by John Wiley & Sons, Ltd.

Red color filter in an organo-soluble polyamide matrix for liquid crystal displays

A red color filter was laminated from a solution of red color pigment and an organo-soluble polyamide, based on 1,4-bis(3,4-dicarboxyphenoxy) benzene dianhydride (HQDPA) and 2,2'-dimethyl-4,4'-methylene dianiline (DMMDA). The red color filter in a polyamide matrix with negative birefringence plays an important role in twisted nematic liquid crystal displays (TN-LCDs). The red color filter, and also compensation films, extend the viewing angle of LCDs. (C) 1997 Elsevier Science S.A.

Fractal roughness characterization of super-ground Mn-Zn ferrite single crystals

The surface of superground Mn-Zn ferrite single crystal may be identified as a self-affine fractal in the stochastic sense. The rms roughness increased as a power of the scale from 10(2) nm to 10(6) nm with the roughness exponent alpha = 0.17 +/- 0.04, and 0.11 +/- 0.06, for grinding feed rate of 15 and 10 mu m/rev, respectively. The scaling behavior coincided with the theory prediction well used for growing self-affine surfaces in the interested region for magnetic heads performance. The rms roughnesses increased with increase in the feed rate, implying that the feed rate is a crucial grinding parameter affecting the supersmooth surface roughness in the machining process.

STM OF FOLDED AND UNFOLDED HEMOGLOBIN MOLECULES ELECTROCHEMICALLY DEPOSITED ON HIGHLY ORIENTED PYROLYTIC-GRAPHITE

The structural characterization of folded and unfolded haemoglobin has been performed by scanning tunnelling microscopy (STM) for the first time. STM images show an oval-shaped pattern for the folded structure of this protein, and moreover two dimers consisting of one haemoglobin molecule can be clearly discerned. The dimensions of a folded molecule were determined as 6.4 x 5.4 x 0.7 nm(3), which are in good agreement with the known size obtained from X-ray analysis. We have found that unfolding of haemoglobin molecules on the surface of highly oriented pyrolytic graphite (HOPG) can be achieved by electrochemical deposition. The STM analysis indicates clearly that the tertiary structure of the protein was lost by electrochemical deposition, and most of the haemoglobin molecules were almost fully extended and exhibited a twisted rope-like or a rod-like aggregated structure. Our investigation demonstrates the capability of the electrochemical method in denaturing this redox protein and in preparing stable biological samples for use in STM imaging.

SYNTHESES AND CRYSTAL-STRUCTURES OF (C8H8)ND(C5H9C5H4)(THF)(2) AND [(C8H8)GD(C5H9C4H4(THF)][(C8H8)GD(C5H9C5H4(THF)(2)]

LnCl(3) (Ln = Nd, Gd) reacts with C5H9C5H4Na (or K2C8H8) in THF (C5H9C5H4 = cyclopentylcyclopentadienyl) in the ratio of 1:1 to give (C5H9C5H4)LnCl(2)(THF)(n) (or (C8H8)LnCl(2)(THF)(n)], which further reacts with K2C8H8 (or C5H9C5H4Na) in THF to form the title complexes. If Ln = Nd the complex (C8H8)Nd(C5H9C5H4)(THF)(2) (a) was obtained: when Ln = Gd the 1:1 complex [(C8H8)Gd(C5H9C5H4)(THF)][(C5H8)Gd(C5H9C5H4)(THF)(2)] (b) was obtained in crystalline form. The crystal structure analysis shows that in (C8H8)Ln(C5H9C5H4)(THF)(2) (Ln = Nd or Gd), the Cyclopentylcyclopentadienyl (eta(5)), cyclooctatetraenyl (eta(8)) and two oxygen atoms from THF are coordinated to Nd3+ (or Gd3+) with coordination number 10. The centroid of the cyclopentadienyl ring (Cp') in C5H9C5H4 group, cyclooctatetraenyl centroid (COT) and two oxygens (THF) form a twisted tetrahedron around Nd3+ (or Gd3+). In (C8H8)Gd(C5H9C5H4)(THF), the cyclopentyl-cyclopentadienyl (eta(5)), cyclooctatetraenyl (eta(8)) and one oxygen atom are coordinated to Gd3+ with the coordination number of 9 and Cp', COT and oxygen atom form a triangular plane around Gd3+, which is almost in the plane (dev. - 0.0144 Angstrom).

亚历山大藻分子鉴定和荧光原位杂交检测方法研究

近年来，世界沿海国家有害赤潮发生的频率、规模及危害都有上升趋势，有害赤潮已经成为重要的近海环境问题之一。要有效防范有害赤潮带来的危害效应，建立和发展可靠、有效的赤潮监测手段非常重要。目前，对于赤潮藻种的监测主要依靠显微观察的方法，在实际应用中经常遇到困难。首先，亲缘关系相近的物种在形态上差异很小，如甲藻门亚历山大藻属的一些种类，仅细胞壁上个别甲片的结构有细微差别，并且这些形态学指标还容易受环境条件及生长阶段的影响。另外，这种以形态学为基础的分析方法，分析速度慢、耗时长，对操作人员的要求较高，难以满足浮游植物种群动力学监测“量大、连续”的要求。因此，本研究将分子生物学的技术和方法应用于赤潮监测，力求提高赤潮藻种鉴定的准确性和检测工作的效率。 亚历山大藻是一类重要的有害赤潮藻，该藻属中一些产毒特性差别很大的藻种，单从表形特征难以明确区分，从而限制了基于形态观察的监测技术的应用。本研究中，我们尝试应用分子生物学技术与方法，开展了该藻属藻种分子鉴定和荧光原位杂交检测方法的研究。在亚历山大藻的分子鉴定方面，我们采用了核糖体RNA基因（rDNA）序列分析的方法，首次测定了9株分离自中国沿海的（以及实验室保有的其它两株）亚历山大藻的rDNA序列全长，其中包括核糖体小亚基（SSU）rDNA、大亚基（LSU）rDNA、5.8S rDNA及内转录间隔区（ITS）区序列。序列分析结果显示，这些藻株包含了5种核糖体类型，分别是塔玛复合种亚洲温带（Temperate Asian）核糖体类型（TSC-TA），塔玛复合种西欧（West European）核糖体类型（TSC-WE），相关亚历山大藻（A. affine）核糖体类型（AF），微小亚历山大藻（A. minutum）葡萄牙（Portugal）核糖体类型（M-PO）和微小亚历山大藻新西兰（New Zealand）核糖体类型（M-NZ）。将测获的rDNA序列划分为若干保守性不同的区段，分别进行系统发育分析（结合GenBank数据库中保存的其它亚历山大藻相关序列）。结果显示，LSU rDNA D1-D2区是对该藻属藻种进行分子鉴定和系统发育研究的较好区段。同时，为解决建立亚历山大藻克隆培养的困难，我们应用单细胞rDNA序列分析方法，对亚历山大藻单个细胞直接进行了种类鉴定。结果表明，该方法适用于不同生活史阶段的亚历山大藻。 在亚历山大藻的检测技术方面，我们进一步扩展和完善了针对完整细胞的荧光原位杂交检测方法。首先，通过对不同核糖体类型藻株rDNA序列信息的对比分析，针对各自特异的序列位点，设计了特异性rRNA标记探针。经荧光原位杂交实验检验，实现了对5种核糖体类型亚历山大藻的特异性标记。其中，针对WE、M-PO及M-NZ核糖体型的特异性探针为首次获得，另外两个探针是针对TA和AF核糖体类型rRNA新的位点所设计。同时，对影响探针标记效果的诸多因素进行了分析和探讨。此外，在2007年春季长江口海域赤潮调查中，首次应用特异性核酸探针和荧光原位杂交检测方法，调查了该海域亚历山大藻的丰度。结果表明，在4月4日-4月10日的样品中，亚历山大藻达到了较高的密度，最高密度达到103cells/L。同时发现，实验中样品的保存方法有待改进。随后的研究表明，盐醇固定方法及多聚甲醛/甲醇固定方法，可以较好的保持rRNA不被降解并适宜杂交（至少3个月时间）。 总之，本研究首次测定并分析了11株亚历山大藻（9株分离自中国沿海）的rDNA全序列信息。在此基础上，获得了5种核糖体类型亚历山大藻的特异性rRNA标记探针，其中3种为首次获得。另外，实验证明，单细胞rDNA分析技术和荧光原位杂交检测方法，在自然水体中亚历山大藻的直接鉴定及丰度调查中，均具有良好的应用前景。这一工作为我国近海亚历山大藻的鉴定和检测提供了理论依据和方法学基础，希望对该藻赤潮的监测工作有推动作用。 关键词：亚历山大藻 遗传探针 rRNA rDNA 荧光原位杂交 系统发育

亚历山大藻（非PSP产毒株）毒理的初步研究

本文以一株不产PSP毒素的相关亚历山大藻（AC-1）为对象，研究了该藻株对褶皱臂尾轮虫、卤虫、黑褐新糠虾急性毒性效应和对糠虾的慢性毒性影响，同时对AFT毒素成分进行了研究，研究结果如下： 通过相关亚历山大藻（AC-1）对褶皱臂尾轮虫、卤虫、黑褐新糠虾的急性毒性影响研究，发现随着相关亚历山大藻（AC-1）密度的升高，轮虫、卤虫、糠虾的存活率逐渐降低，其96hLC50分别为：1500cells/ml，90cells/ml，5000cells/ml。比较研究三种生物对相关亚历山大藻（AC-1）敏感性可以看出，三种生物对该藻的敏感性顺序为：卤虫>轮虫>糠虾。 相关亚历山大藻（AC-1）对黑褐新糠虾的生长及种群繁殖有显著影响，我们发现在密度为50cells/ml藻液中，糠虾的繁殖就受到了不利影响。实验进行到63d结束时，糠虾日最高产虾数、总产幼虾数、总产虾天数都明显减少，初次产虾时间推迟，繁殖中断增加。且该藻对黑褐新糠虾亲虾的存活、生长也有一定的影响，糠虾亲虾的存活率为对照的71%，而体长和体重分别为对照组的87.3%和97.8%，但差异尚不显著（P>0.05）。 研究相关亚历山大藻（AC-1）各组分的毒性（藻液、藻细胞重悬液、藻细胞培养过滤液、内容物），发现藻液和藻细胞重悬液对褶皱臂尾轮虫种群数量及轮虫、卤虫、糠虾的存活率均有显著影响，表明相关亚历山大藻活体藻细胞的毒性最强。过滤液和内容物也显著降低了轮虫和卤虫的存活率，其对糠虾也有影响，但不显著，表明AFT毒素可能来源于细胞内，能分泌到细胞培养液中。 研究相关亚历山大藻（AC-1）AFT毒素的热稳定性、酸碱稳定性、去蛋白组分毒性、分子量范围、极性、多糖组分鉴定，表明AFT毒素为极性较强的多糖类物质，对热和酸碱是稳定的，其分子量范围在5K~50K之间。 以上结果表明相关亚历山大藻（AC-1）虽然不产生PSP毒素，但能产生极性多糖类毒素，对甲壳类等浮游动物的种群数量和资源补充产生不利影响。本研究为以后进一步研究AFT毒素的作用机制和毒素的化学结构奠定了基础，为全面评价亚历山大藻赤潮的危害提供了科学依据。

基于仿射不变特征的图像匹配

图像匹配是计算机视觉中的一个重要研究领域，无论在民用还是军用上都有着重要的应用价值。本文以研究室国防重点预研究项目自动目标识别为背景，采用图像匹配方法，实现飞行器定位导航。具体工作流程是：事先利用侦察手段获取飞行器途经下方的地物景象(基准图)并存于飞行器载计算机中，然后当携带相应传感器的飞行器飞过预定的位置范围时，拍摄当地的地物景象(实时图)，将实时图和基准图在飞行器载计算机中进行匹配比较，可确定当前飞行器的准确位置，完成定位导航功能。 由于对同一场景使用相同或不同的传感器(成像设备)，以及在不同条件下(天候、照度、摄像位置和角度等)成像的复杂性和多样性等困难的存在，传统的相关匹配方法对上述困难的克服在方法原理上存在先天不足，所以无法胜任。故本文采用的方法是基于局部不变量特征的图像匹配。局部不变量特征因为能更灵活地描述图像，有效地处理图像复杂和遮挡问题，所以基于局部不变量特征的图像匹配方法对于视点的大变化，图像背景变化，以及目标场景识别等都有较好的效果。 基于局部不变量特征的图像匹配方法的步骤通常分为三部分：(1)用图像区域检测算子提取图像相关区域，(2)构造合适的特征描述区域，(3)选择特征相似度度量准则实现图像区域特征的匹配。本文详细研究了最大稳定极值区域 (MSER)方法，在此基础上进行了改进，具体工作如下：(1)利用高斯核函数对图像平滑采样，建立图像的高斯尺度空间，(2)在图像的高斯尺度空间中，利用MSER检测算子检测出图像在不同尺度下的所有仿射相关区域，(3)由于区域不规则，再用仿射不变的椭圆拟合并归一化，这时所有的区域仅存在旋转的不同，(4)用SIFT特征描述图像区域，得到所有区域的128维特征向量集。(5)采用欧式距离度量特征间的相似度，以最近邻和次近邻的比值作为特征匹配准则进行匹配。 本论文的主要研究工作在于把图像的高斯尺度空间引入到MSER算法中，进而大大改善了MSER算法对于图像的尺度变换、仿射变换以及图像模糊的性能。由于建立了高斯尺度空间，增加了MSER检测算子检测的范围，所以使得改进算法的性能得到了改善。论文第四章给出四组实验，分别为尺度变换，仿射变换，图像模糊和大视点变换。最后通过对匹配结果正确数量和错误数量的统计，论证了改进方法的性能要好于MSER算法。通过对算法复杂度的分析，得出虽然在改进算法引入了图像的高斯尺度空间，但是算法复杂度却并未增加，与MSER算法相同，为O(nloglogn)。

仿射非线性系统的广义逐点最小范数控制

在Freeman的逐点最小范数控制器的基础上,提出了一种新的非线性控制器设计框架-广义逐点最小范数控制器,并证明了其连续性.通过一个引导函数,新的控制器可以和其他的控制器设计策略结合,从而大大提高了控制器设计的灵活性.另外,给出了新方法的两个应用:改善局部线性化控制器稳定域较小的缺陷;及和其它控制器设计方法结合,使之能够简单有效地处理具有输入约束的系统.