现代加筋土技术应用与研究进展

对土工合成材料研究与应用概况、加筋土的国内外应用与研究进展、加筋土基本理论研究进展进行了综合分析,提出了今后研究工作的重点。     

分子工程学

分子工程学以体系的功能为导向,在分子水平上进行结构设计与施工,探索功能、结构与合成三者之间的关系原理,发展合成、制备与组装方法学,研究结构基元本征性质和构效关系。本文讨论了建设分子工程学这一新学科的重要性,介绍了自发单层分散原理与CO吸附剂、纳米结构光电功能体系、金属纳米簇基催化剂、表面分子多孔网络的精确可控组装以及功...     

Identification of [PtCl2(phen)] binding modes in amyloid-β peptide and the mechanism of aggregation inhibition

Platinum phenanthroline complexes inhibit amyloid-β (Aβ) aggregation and reduce Aβ-caused neurotoxicity [Proc. Natl. Acad. Sci., 2008, 105, 6813-6818]. In this study, we investigated the interactions of Aβ(1-16) with [PtCl(2)(phen)] (phen=1,10-phenanthroline) using HPLC, ESI-MS, and NMR spectroscopy , and characterized the identity of products using tandem mass spectrometry. Results indicated that the phenanthroline ligand could induce noncovalent interactions between Aβ peptide and platinum complexes, leading to rapid Aβ platination. Multiple products were generated in the reaction, in which His6/His14 chelation was preferentially formed. Coordination of Asp7, His13, and Lys16 was also detected in other products. The majority of products were monoplatinated adducts with binding of the {Pt(phen)} scaffold, which impeded intermolecular interactions between Aβ peptides. Moreover, noncovalent interactions were confirmed by the interaction between Aβ peptide and [Pt(phen)(2)]Cl(2). The synergistic roles of the phen ligand and platinum(II) atom in the inhibition of Aβ aggregation are discussed.     

Doubly hydrophilic multiarm hyperbranched polymers with acylhydrazone linkages as acid-sensitive drug carriers

A novel type of drug carrier capable of controlled drug release is proposed. It consists of an acid-sensitive doubly hydrophilic multiarm hyperbranched copolymer with a hyperbranched polyamidoamine core and many linear poly(ethylene glycol) arms. Using pH-sensitive acylhydrazone linkages, the polymer forms unimolecular micelles that can encapsulate hydrophobic drugs. Due to their amphiphilicity, the drug-loaded unimolecular micelles can self-assemble into multimolecular micelles that show acid-triggered intracellular delivery of the hydrophobic drugs.     

Total synthesis of (-)-cocaine and (-)-ferruginine

Total synthesis of tropane alkaloids (-)-cocaine and (-)-ferruginine were accomplished in nine steps each and in 55% and 46% overall yields, respectively, starting from the known Betti base derivative (+)-(7aR,10R,12S)-10-(1H-benzotriazol-1-yl)-7a,8,9,10-tetrahydro-12-phenyl-12H-naphtho[1,2-e]pyrrolo[2,1-b][1,3]oxazine. In this novel route, RCM reaction and 1,3-dipolar cycloaddition were employed as key steps for the enantioselective construction of tropane skeleton and the regioselective introduction of 3-bromo-2-isoxazoline ring as masked cis-2,3-disubstituents. To obtain the desired precursor (2S,5R)-2-allyl-5-vinylpyrrolidine for RCM reaction, we developed a general and practical method for the preparation of enantiopure cis-2,5-disubstituted pyrrolidines bearing alkene- and/or alkyne-containing substituents. We also offered two highly efficient pathways for the conversion of the 3-bromo-2-isoxazoline ring into the desired cis-2,3-disubstituted groups in (-)-cocaine and (-)-ferruginine.     

四磺基钴酞菁/MCM-41的制备、表征及其催化性能

将四磺基钴酞菁（CoTSPc）通过共价结合连接在氨基化的介孔分子筛MCM-41孔道壁上，制成负载酞菁催化剂，对其进行了X射线衍射（XRD）和红外分析，并研究了其对巯基乙醇的催化氧化反应动力学．结果表明，负载酞菁催化剂有优良的催化性能，在液相反应过程中扩散阻力较小．这种负载催化剂有酶催化特点，即遵循米氏动力学规律，米氏常数Km为0．015mol／L．反应完成后，通过沉淀即可从反应体系中分离，解决了酞菁催化剂无法回收利用和对环境造成新的污染的问题．在工业生产和环境保护方面有着良好应用前景．     

基于过模波导的高功率微波准相干功率合成器

研究了一种用于功率合成的GW级高功率微波功率合成器。该合成器工作在X波段,输入微波由2路工作频率不同的X波段的微波源产生。为了满足输出功率和功率容量的要求,用于功率合成的微波源工作段波导的过模因子为12.7,这给功率合成器的设计带来了一定的困难。着重讨论了如何利用过模波导设计X波段高功率合成器,研究了如何抑制过模波导的高次模式并提高其功率容量和传输效率。设计的功率合成器单路传输效率达到99.0%以上,允许的最大输出功率达到5.6 GW以上,还可以按照需求适当增大高度,以进一步提高其功率容量而不影响传输效率。     

刻槽结构高功率微波输出窗次级电子倍增效应

从理论上分析了周期性矩形刻槽对喇叭天线输出窗真空侧次级电子倍增的影响。采用动力学方法分析得到电子沿介质窗表面运动的渡越时间和碰撞能量,验证得到一定尺寸的矩形刻槽介质窗可以有效抑制次级电子倍增效应。在此情况下,对比了刻槽和不刻槽两种输出窗的辐射特性,发现周期2 mm、宽度1 mm、深度1 mm的矩形刻槽对介质窗辐射特性的影响可以忽略。     

X波段高功率微波选模定向耦合器

高功率、长脉冲是高功率微波技术发展的趋势,提高微波器件的功率容量成为一项重要的任务,使用过模器件可以有效提高微波源的功率容量,然而却会带来微波源中同时存在多种模式的问题。为了识别一个X波段长脉冲过模高功率微波源的输出主模TM01模式,设计了一种在线选模定向耦合器,进行了理论分析和模拟优化设计。当频率范围为9.2~9.6 GHz时,模拟结果显示该选模耦合器对TM01模的耦合度为-54 dB,在400 MHz带宽内定向性大于35 dB,对TM02模的抑制度大于15 dB,功率容量可达到3 GW以上。     

Continuous and Segmented Semiconducting Fiber-like Nanostructures with Spatially Selective Functionalization by Living Crystallization-Driven Self-Assembly

Fiber-like π-conjugated nanostructures are important components of flexible organic electronic and optoelectronic devices. To broaden the range of potential applications, one needs to control not only the length of these nanostructures, but the introduction of diverse functionality with spatially selective control. Here we report the synthesis of a crystalline-coil block copolymer of oligo(p-phenylenevinylene)-b-poly(2-vinylpyridine) (OPV₅-b-P2VP₄₄), in which the basicity and coordinating/chelating ability of the P2VP segment provide a landscape for the incorporation of a variety of functional inorganic NPs. Through a self-seeding strategy, we were able to prepare monodisperse fiber-like micelles of OPV₅-b-P2VP₄₄ with lengths ranging from 50 to 800 nm. Significantly, the exposed two ends of OPV core of these fiber-like micelles remained active toward further epitaxial deposition of OPV₅-b-PNIPAM₄₉ and OPV₅-b-P2VP₄₄ to generate uniform A-B-A and B-A-B-A-B segmented block comicelles with tunable lengths for each block. The P2VP domains in these (co-)micelles can be selectively decorated with inorganic and polymeric nanoparticles as well as metal oxide coatings, to afford hybrid fiber-like nanostructures. This work provides a versatile strategy toward the fabrication of narrow length dispersity continuous and segmented π-conjugated OPV-containing fiber-like micelles with the capacity to be decorated in a spatially selective way with varying functionalities.