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991.
The data on synthesis of individual and heterometallic alkoxide and oxoalkoxide derivatives of rhenium are summarized. Their structures are considered, characteristic features and peculiarities of the structures are analyzed. Data on the thermal decomposition of rhenium alkoxides and its application for the preparation of rhenium-based metallic and oxide materials are given. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2177–2188, October, 2005.  相似文献   
992.
A novel blue light-emitting polyfluorene-based copolymer PTHD containing electron-rich triphenylamine and electron-poor phenylquinoline side chains in the C-9 position of fluorene unit is described. By comparison of the solution and thin film photoluminescence (PL) spectra of PTHD, a considerable red-shift of Δλ = 10-15 nm was observed in the thin film PL spectrum. The emission intensity of the shoulder peak appeared in dilute solution was also significantly enhanced in the thin film. In contrast to the reference polymer poly{[9,9-dihexylfluorene]-alt-[9,9-di(2,4-diphenylquinoline)fluorene]}, PTHD exhibits higher HOMO energy level, and higher maximum brightness with the PLED device configuration of ITO/PEDOT:PSS/polymer70% + PBD30%/TPBI/LiF/Al.  相似文献   
993.
A quantitative and fast method of dissolution of refractory thoria (ThO2) was developed for the determination of thorium (Th) in a given sample. The dissolution of sintered ThO2 powder, microspheres and pellets using 88% phosphoric acid was investigated. The conditions of quantitative dissolution of ThO2 microspheres were optimized by conventional heating in autoclave and also by microwave heating. 100 mg of sintered ThO2 microspheres were dissolved in 8 g of phosphoric acid in an autoclave, and heating at 170 °C for 3 h, in comparison to 5 g of phosphoric acid by microwave heating (375 W) at 220 °C for 1 h. Dissolution studies on the powder form of sintered ThO2 were also performed. 1 g of sintered ThO2 powder could be dissolved in 6.5 g of phosphoric acid in autoclave heating at 170 °C for 1 h. Strong complexing of (PO4)3− with Th4+ may be the influencing factor for quantitative dissolution of ThO2.  相似文献   
994.
The Yb3+-doped LiGd(MoO4)2 crystal with the size up to Φ20×30 mm3 has been grown by Czochralski technique.The polarized room temperature absorption and emission spectra have been investigated.This crystal exhibits a broad absorption band centered at 975 nm with an FWHM of 43 and 59 nm for π-and σ-polarization,respectively,and the corresponding maximal absorption cross-sections are 3.36 and 2.42×10-20 cm2.The emission broadband has an FWHM of 47 and 54 nm for π-and σ-polarization,respectively,with the corresponding emission cross sections of 3.92 and 3.34 × 10-20 cm2 at 1020 nm.The measured fluorescence lifetime is 287 μs.  相似文献   
995.
高分子电致发光材料研究进展   总被引:1,自引:0,他引:1  
综述了近几年来国内外关于高分子聚合物在电致发光材料领域的研究进展,重点介绍了聚苯撑乙烯、聚芴类、聚噻吩类聚合物及其衍生物的相关研究成果,并讨论了当前高分子电致发光材料存在的关键问题及应用前景.  相似文献   
996.
Hollow silica microspheres(HSMSs) have been successfully fabricated via a facile hydrothermal route using D-glucose as the sacrificial template and sodium silicate powder as the silica precursor.The resulting silica hollow particles were characterized by scanning electron microscopy(SEM),transmission electron microscopy(TEM),X-ray diffraction(XRD),and infrared spectroscopy(IR).The surface area was determined using the BET method.SEM and TEM images exhibited micro-sized silica hollow particles with a size of ~1.5μm.  相似文献   
997.
In the present work,an interconnected sandwich carbon/Si-SiO2/carbon nanospheres composite was prepared by template method and carbon thermal vapor deposition(TVD).The carbon conductive layer can not only efficiently improve the electronic conductivity of Si-based anode,but also play a key role in alleviating the negative effect from huge volume expansion over discharge/charge of Si-based anode.The resulting material delivered a reversible capacity of 1094 mAh/g,and exhibited excellent cycling stability.It kept a reversible capacity of 1050 mAh/g over 200 cycles with a capacity retention of 96%.  相似文献   
998.
Mesoporous SnO microspheres were synthesised by a hydrothermal method using NaSO4 as the morphology directing agent. Field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and high‐resolution transmission electron microscopy (HRTEM) analyses showed that SnO microspheres consist of nanosheets with a thickness of about 20 nm. Each nanosheet contains a mesoporous structure with a pore size of approximately 5 nm. When applied as anode materials in Na‐ion batteries, SnO microspheres exhibited high reversible sodium storage capacity, good cyclability and a satisfactory high rate performance. Through ex situ XRD analysis, it was found that Na+ ions first insert themselves into SnO crystals, and then react with SnO to generate crystalline Sn, followed by Na–Sn alloying with the formation of crystalline NaSn2 phase. During the charge process, there are two slopes corresponding to the de‐alloying of Na–Sn compounds and oxidisation of Sn, respectively. The high sodium storage capacity and good electrochemical performance could be ascribed to the unique hierarchical mesoporous architecture of SnO microspheres.  相似文献   
999.
Controlled organization of polymer chains into ordered structures is highly important to tune or enhance the properties of the polymeric materials. A supramolecular approach using host–guest chemistry has allowed rational design of chain assemblies with many functional properties. Nanoporous materials with ordered channel structures are particularly useful for attaining precise assemblies of polymer chains through nanoconfinement.  相似文献   
1000.
New organosilica precursors containing two triethoxysilyl groups suitable for the organosilica material formation through the sol‐gel process were designed and synthesised. These precursors display alkyne or azide groups for attaching targeted functional groups by copper‐catalysed azide–alkyne cycloaddition (CuAAC) and can be used for the preparation of functional organosilicas following two strategies: 1) the functional group is first appended by CuAAC under anhydrous conditions, then the functional material is prepared by the sol‐gel process; 2) the precursor is first subjected to the sol‐gel process, producing porous, clickable bridged silsesquioxanes or periodic mesoporous organosilicas (PMOs), then the desired functional groups are attached by means of CuAAC. Herein, we show the feasibility of both approaches. A series of bridged bis(triethoxysilane)s with different pending organic moieties was prepared, demonstrating the compatibility of the first approach with many functional groups. In particular, we demonstrate that organic functional molecules bearing only one derivatisation site can be used to produce bridged organosilanes and bridged silsesquioxanes. In the second approach, clickable PMOs and porous bridged silsesquioxanes were prepared from the alkyne‐ or azide‐containing precursors, and thereafter, functionalised with complementary model azide‐ or alkyne‐containing molecules. These results confirmed the potential of this approach as a general methodology for preparing functional organosilicas with high loadings of functional groups. Both approaches give rise to a wide range of new functional organosilica materials.  相似文献   
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