(Ph_3P)_2(CO)RuC_(60)的合成及结构表征

过渡金属—Ｃ６０配合物的合成及结构的研究是Ｃ６０化学非常重要的一个组成部分，这对于发展Ｃ６０化学及新型功能材料的开发具有很大意义．关于这方面的研究工作近年已有一些报道〔１～３〕．Ｈａｗｋｉｎｓ等关于（ｔＢｕＣ６Ｈ５Ｎ）２ＯｓＯ４（Ｃ６０）的合成及单...     

基于一种新型超腔的高亮度激光同步辐射分析

 提出了一种由一对抛物面构成的超腔的技术方案,计算了超腔汇聚点处的总光子密度。利用康普顿散射理论对基于抛物面超腔的激光同步辐射及其光子产额进行了讨论和计算。结果表明:当超腔镜面的反射率等于99.99%时,在超腔碰撞点处的总光子数密度大约是初始激光束在碰撞点处光子数密度的5 000倍,对应康普顿垂直散射的光子产额大约是电子束与初始激光束在碰撞点处发生康普顿垂直散射时的5 000倍。     

大型火箭起飞横向漂移测量系统研究

本文论及了大型火箭发射起飞段横向漂移量的近距离高速摄影测量系统和数据处理方法。     

间歇式高速摄影机的分辨率

文中讨论了间歇式高速摄影机分辨率的计算方法.     

Direct Synthetic Processes for Cyclic Carbonates from Olefins and CO<Subscript>2</Subscript>

This short review presents the recent developments in the direct synthesis of cyclic carbonates from olefins and CO₂. The straightforward synthesis of cyclic carbonates from olefins instead of epoxides, also called one-pot “oxidative carboxylation” of olefins, can be viewed as the coupling of two sequential reactions of epoxidation of olefins and CO₂ cycloaddition to epoxides formed. The facile synthetic approach would make carbonate synthesis simpler and even cheaper with industrial potential from environmental and economic points of view. Some progresses have been made on this direct synthetic reaction for cyclic carbonates with homogeneous and heterogeneous catalysts, however, this reaction system is still at a preliminary stage. Among the catalysts reported, only a few can be considered as effective for the direct oxidative carboxylation of olefins to cyclic carbonates. Thus active and selective catalysts should be explored to put the direct synthesis of cyclic carbonates into practical applications.     

Folic acid-conjugated GdPO<Subscript>4</Subscript>:Tb<Superscript>3+</Superscript>@SiO<Subscript>2</Subscript> Nanoprobe for folate receptor-targeted optical and magnetic resonance bi-modal imaging

Both fluorescent and magnetic nanoprobes have great potential applications for diagnostics and therapy. In the present work, a folic acid-conjugated and silica-modified GdPO₄:Tb³⁺ (GdPO₄:Tb³⁺@SiO₂-FA) dual nanoprobe was strategically designed and synthesized for the targeted dual-modality optical and magnetic resonance (MR) imaging via a facile aqueous method. Their structural, optical, and magnetic properties were determined using transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR), ultraviolet-visible spectra (UV-Vis), photoluminescence (PL), and superconducting quantum interference device (SQUID). These results indicated that GdPO₄:Tb³⁺@SiO₂-FA were uniform monodisperse core-shell structured nanorods (NRs) with an average length of ~200 nm and an average width of ~25 nm. The paramagnetic property of the synthesized GdPO₄:Tb³⁺@SiO₂-FA NRs was confirmed with its linear hysteresis plot (M-H). In addition, the NRs displayed an obvious T₁-weighted effect and thus it could potentially serve as a T₁-positive contrast agent. The NRs emitted green lights due to the ⁵D₄ → ⁷F₅ transition of the Tb³⁺. The in vitro assays with NCI-H460 lung cancer cells and human embryonic kidney cell line 293T cells indicated that the GdPO₄:Tb³⁺@SiO₂-FA nanoprobe could specifically bind the cells bearing folate receptors (FR). The MTT assay of the NRs revealed that its cytotoxicity was very low. Further in vivo MRI experiments distinctively depict enhanced anatomical features in a xenograft tumor. These results suggest that the GdPO₄:Tb³⁺@SiO₂-FA NPs have excellent imaging and cell-targeting abilities for the folate receptor-targeted dual-modality optical and MR imaging and can be potentially used as the nanoprobe for bioimaging.     

Easily Separated and Recyclable Amino-functionalized PorousSiO2 Beads with 3D Continuous Meso/Macropore Channels

Amino-functionalized porous SiO₂ beads with a diameter of 200—800 μm(PSB-NH₂) have been successfully synthesized by grafting 3-aminopropyl-triethoxysilane onto meso/macroporous silica beads(PSB), in which the PSB was prepared by hydrothermal synthetic method with a porous hard template anion-exchange resin. The as-prepared materials were characterized by means of nitrogen sorption and transmission electron micrographs(TEM), showing the presence of 3D interconnected and continuous large mesopores and macropores inside. The beads were used to catalyze Knoevenagel condensation and proved to be highly active and selective due to the high accessibility of the reactants to the amino groups via the continuous 3D meso/macopores. Notably, such material in bead format facilitates the extremely straightforward separation from reaction solution without any centrifugation or filtration. Moreover, PSB-NH₂ proved to be a stable catalyst via leaching experiment test, and can be easily recovered and reused without significant loss of activity in successive catalytic cycles.     

Synthesis of Submicrometer-sized Sn-MCM-41 Particles and Their Catalytic Performance in Baeyer-Villiger Oxidation

Submicrometer-sized tin-containing MCM-41 particles with a size of several hundred nanometers(Sn-MCM-41/SMPs) were rapidly prepared with tin chloride as tin source and tetraethyl orthosilicate as silicon source via a dilute solution route in sodium hydroxide medium at room temperature. The characterization results show the highly ordered hexagonal mesopores and tetrahedral Sn species in Sn-MCM-41/SMPs. The material proved to be active and selective for Baeyer-Villiger oxidation of adamantanone with aqueous H₂O₂. Notably, Sn-MCM-41/ SMPs displayed a higher initial reaction rate and turnover number(TON) than common micrometer-sized Sn-MCM-41 large particles(Sn-MCM-41/LPs), mainly attributed to the accelerated diffusion of the reactants and enhanced accessibility to the catalytic Sn species via shorter mesopore channels in Sn-MCM-41/SMPs. Furthermore, Sn-MCM-41/SMPs could be reused without the loss of activity after five runs, indicating that Sn active sites in the submicrometer-sized particles are remarkably stable. The study shows that decreasing particle size of Sn-MCM-41 in submicrometer scale is an effective way to achieve catalysts for Baeyer-Villiger oxidations with improved catalytic performance.