UV laser deposition of nanostructured Si/C/O/N/H from disilazane precursors and evolution to silicon oxycarbonitride

Megawatt ArF laser photolysis of gaseous methyldisilazanes [(CH₃)_nH_3?nSi]₂NH (n = 2, 3) in excess of Ar yields hydrocarbons (major volatile products), methylsilanes (minor volatile products) and allows chemical vapour deposition of solid amorphous Si/C/O/N/H powder containing Si? X (X? C, H, O, N) bonds. The incorporation of O is due to a high reactivity of the primarily formed products towards air moisture. The resulting solid materials possess nanometer‐sized texture and high specific area, contain Si‐centered radicals and anneal under argon to silicon oxycarbonitride, whose structure is described as a network of O‐ and N‐interconnected Si and C atoms. Copyright © 2006 John Wiley & Sons, Ltd.     

二羰基环戊二烯基（三环己基锡基）铁的晶体结构

关于（三烃基锡基）二数基环戊二烯基铁类配合物的合成反应已进行了许多研究D'，并发现某些这类配合物具有一定的催化聚合作用或抗肿瘤活性［'·'j．这类配合物中已见报道晶体结构的只有烃基为三苯基作配体时的配合物CP（CO）。FesnPh。D'，为了便于比较及研究结构和性能的关系，我们以三环已基为锡的配体，以与文献［'j中近似的方法合成了配合物CP（CO）。Fesfl（C6HI人，并进行了IR、NMR的测定．X光四圆衍射仪对所得单晶的结构测定结果表明，该配合物具有与CP（CO）。F。SnPh。相近的晶体结构．1标题配合物的制备与谱学表征1…     

Structure of Framework Aluminum Lewis Sites and Perturbed Aluminum Atoms in Zeolites as Determined by 27Al{1H} REDOR (3Q) MAS NMR Spectroscopy and DFT/Molecular Mechanics

Zeolites are highly important heterogeneous catalysts. Besides Brønsted SiOHAl acid sites, also framework Al_FR Lewis acid sites are often found in their H‐forms. The formation of Al_FR Lewis sites in zeolites is a key issue regarding their selectivity in acid‐catalyzed reactions. The local structures of Al_FR Lewis sites in dehydrated zeolites and their precursors—“perturbed” Al_FR atoms in hydrated zeolites—were studied by high‐resolution MAS NMR and FTIR spectroscopy and DFT/MM calculations. Perturbed framework Al atoms correspond to (SiO)₃AlOH groups and are characterized by a broad ²⁷Al NMR resonance (δ_i=59–62 ppm, C_Q=5 MHz, and η=0.3–0.4) with a shoulder at 40 ppm in the ²⁷Al MAS NMR spectrum. Dehydroxylation of (SiO)₃AlOH occurs at mild temperatures and leads to the formation of Al_FR Lewis sites tricoordinated to the zeolite framework. Al atoms of these (SiO)₃Al Lewis sites exhibit an extremely broad ²⁷Al NMR resonance (δ_i≈67 ppm, C_Q≈20 MHz, and η≈0.1).     

动脉中非平稳流动壁面剪切力及其Hilbert-Huang变换

本文通过数值方法求解均匀动脉中的非平稳脉动流,给出了通过测量非平稳脉动血流量确定壁面切应力的方法.作为算例,采用实测的大鼠颈总动脉流量信号,求出了均匀动脉壁面切应力波形.进一步对求得的切应力波形进行经验模态分解(EMD),得到了切应力波形的各内在模态(IMF),以及Hilbert幅值谱.从切应力波形经Hilbert-Huang变换得到的IMF和Hilbert谱图可以明显地看出切应力各频率成分的物理意义.所得结果为进一步深入研究非平稳脉动切应力与血管重建的关系提供了一种方法学基础.     

Suzuki Reaction of Aryl Bromides Using a Phosphine-Free Magnetic Nanoparticle-Supported Palladium Catalyst

A palladium catalyst immobilized on superparaganetic nanoparticles was prepared with a palladium loading of 0.30 mmol/g. The catalyst was characterized using X-ray diffraction, scanning electron microscopy, transmission electron microscopy, vibrating sample magnetometry, thermogravimetric analysis, Fourier transform infrared, atomic absorption spectrophotometry, and nitrogen adsorption. The immobilized palladium catalyst was an efficient catalyst without added phosphine ligands for the Suzuki cross-coupling reaction of several aryl bromides with phenylboronic acid. The recovery of catalyst was simply by magnetic decantation in the presence of a magnet. The immobilized palladium catalyst can be reused many times without significant degradation in catalytic activity. No leaching of active palladium species into the reaction solution was detected.     

三元TBZ/HPB-铜(Ⅱ)-L-蛋氨酸配合物的合成、表征、抑菌活性及与DNA的作用

本文合成了2个新的三元铜(Ⅱ)配合物:[Cu(TBZ)(L-Met)(H2O)]ClO4.H2O(1)和[Cu(HPB)(L-Met)]ClO4(2)[TBZ=2-(4′-噻唑基)苯并咪唑,HPB=2-(2-吡啶)苯并咪唑,L-Met=L-蛋氨酸]。通过元素分析、摩尔电导率、IR、UV-Vis及电喷雾质谱对这些配合物进行了表征。用二倍稀释法研究了配合物的抗菌活性,发现配合物对金黄色葡萄球菌(Staphylococcus aureus,G+),枯草杆菌(Bacillussubtilis,G+),沙门氏杆菌(Salmonella,G-)和大肠杆菌(Escherichia coil,G-)具有良好的抑制作用。采用电子吸收光谱、荧光光谱、粘度测定及琼脂凝胶电泳方法研究了配合物与DNA的相互作用,结果表明,配合物以插入方式与DNA作用,在维生素C存在下通过羟自由基.OH,单线态氧1O2或者1O2类似物如Cu-O2,切割pBR322 DNA双螺旋结构。     

单调性条件在Fourier级数收敛性中的最终推广:历史、发展、应用和猜想

为了对Fourier级数进行近似计算和有效应用,必须研究其收敛性,这个课题有长久的历史,形成了数学分析中吸引包括许多著名数学家在内的学者研究的一条热烈但困难的主流.其中,在三角级数(Fourier级数)一致收敛性和平均收敛性问题中人们一直关心Fourier系数的单调递减条件最终的推广.这个开始于英国Chaundy-Jollife(1916年)和Young(1913年)的工作最近出现了突破性的进展,产生了许多完善的结果.本文将对这方面的历史、发展给出综述,并重点介绍最近的应用成果,并对以后的工作给出研究思路和线索.     

互补对偶结构的三值ECL锁存器设计

在分析发射极耦合逻辑(ECL)电路的互补对偶特性基础上,指出了差分对的两个开关变量的不独立性及互补对偶特性,并设计了互补对偶结构的ECL三值D型锁存器.这种新型的D型锁存器电路比传统电路具有更简单的电路结构.它的输出是互补的双轨三值输出系统.应用这种新型锁存器设计的D触发器及时序电路将具有更简单的电路结构.     

Quantum crystallites and nonlinear optics

This is a review and analysis of the optical properties of quantum crystallites, with principal emphasis on the electro-optic Stark effect and all optical third order nonlinearity. There are also introductory discussions on physical size regimes, crystallite synthesis, quantum confinement theory, and linear optical properties. The experiments describe CdSe crystallites, exhibiting strong confinement of electrons and holes, and CuCl crystallites, exhibiting weak confinement of the exciton center of mass. In the CdSe system, neither the Stark effect nor the third order nonlinearity is well understood. The Stark shifts appear to be smaller than calculated, and field inducted broadening also occurs. The third order nonlinearity is only modestly stronger than in bulk material, despite theoretical prediction. Unexpectedly large homogeneous widths, due to surface carrier trapping, in the nominally discrete crystallite excited states appear to be involved. The CuCl system shows far narrower spectroscopic homogeneous widths, and corresponds more closely to an ideal quantum dot in the weak confinement limit. CuCl also exhibits exciton superradiance at low temperature. Surface chemistry and crystallite encapsulation are critical in achieving the predicted large Stark and third order optical effects in II-VI and III-V crystallites.     

Electronic transition dipole moments and excited-state alignment in linear molecules,with application to diatomic rare gas halides

The relationship between the direction of transition dipoles and the symmetry of electronic wavefunctions is investigated. In the case of $\text{Ω}\text{=}\text{1}\text{2}\text{?}\text{Ω′}\text{=}\text{1}\text{2}$ transitions, the dipole direction is not determined by symmetry alone. However, in all other cases the directions (parallel or perpendicular) are specified by simple selection rules based upon $\text{ΔΩ}$. In $\text{Ω}\text{=}\text{1}\text{2}\text{Ω′}\text{=}\text{1}\text{2}$ transitions, the transition dipole may accidentally have spherical symmetry, in which case a linearly polarized plane wave photon beam produces an unaligned excited-state distribution. These results are applied to the ultraviolet charge transfer transitions of the diatomic rare gas halides.