Tetraaquabis[5‐(3‐pyridyl‐κN)pyrimidine]zinc(II) bis(trifluoromethanesulfonate): a novel cationic complex and three‐dimensional hydrogen‐bonded network

The title compound, [Zn(C₉H₇N₃)₂(H₂O)₄](CF₃O₃S)₂, contains an octahedral [ZnL₂(H₂O)₄]²⁺ cationic complex with trans geometry (Zn site symmetry ), and each 5‐(3‐pyridyl)pyrimidine (L) ligand is coordinated in a monodentate fashion through the pyridine N atom. In the extended structure, these complexes, with both hydrogen‐bond acceptor (pyrimidine) and donor (H₂O) functions, are linked to each other by intermolecular water–pyrimidine O—H...N hydrogen‐bonding interactions, resulting in a double chain along the crystallographic a axis. The trifluoromethanesulfonate anions are integrated into the chains via O—H...O hydrogen bonds between the coordinated water and sulfonate O atoms. These double chains are associated into a novel three‐dimensional network through interchain water–pyrimidine O—H...N hydrogen bonds. The asymmetric ligand plays an important role in constructing this unusual supramolecular structure.     

How to recognize nonexpansive mappings and isometric mappings

In two real Banach spaces, we shall present two conditions, under one of which each nonexpansive mapping must be an isometry.     

Completion of R2 with a Conformal Metric as a Closed Surface

In this paper,we obtain some asymptotic behavior results for solutions to the prescribed Gaussian curvature equation.Moreover,we prove that under a con-formal metric in R2,if the total Gaussian curvature is 4π,the conformal area of R2 is finite and the Gaussian curvature is bounded,then R2 is a compact C1,α surface after completion at ∞,for any α ∈(0,1).If the Gaussian curvature has a Holder decay at in-finity,then the completed surface is C2.For radial solutions,the same regularity holds if the Gaussian curvature has a limit at infinity.     

数字全息图取样模型的简化研究

数字全息研究领域目前存在两种不同的数字全息图取样模型.按照这两种模型进行研究时, 不但涉及较复杂的数学运算, 在许多情况下还会导致不同的研究结果, 不便于理论分析及实际应用.基于对数字全息图记录的物理过程分析及电荷藕合器件(charge coupled device, CCD)几何结构的研究, 本文将这两种取样模型简化为相同的数学表达式. 利用数字全息图的余弦级数展开及取样定理对简化模型的研究表明, 简化模型不但具有清晰的物理意义, 而且可以方便地为应用研究服务. 基于简化模型对物光波通过光学系统到达CCD的数字全息记录系统进行了研究, 导出得到实验证实的波前重建表达式. 关键词： 数字全息 波前重建 相干光成像     

世界卫生保健状况评价的统计分析

本文针对反映卫生保健状况的各项指标数据,首先利用数理统计中因子分析的方法,找出反映卫生保健状况的综合因子,并计算各个国家的因子得分,然后根据子得分对各国分别进行排名,最后再用聚类法给出世界卫生保健状况的等级平价。并为促进世界卫生保健事业的发展提出几点建议。     

Fluorescence ratiometric pH sensor prepared from covalently immobilized porphyrin and benzothioxanthene

A fluorescence ratiometric sensor for pH determination is described in this paper. The sensor incorporated the pH-sensitive dye meso-5,10,15,20-tetra-(4-allyloxyphenyl)porphyrin (TAPP) as an indicator and a pH-insensitive dye N-(2-methacryloxyethyl)benzo[k,l]thioxanthene-3,4-dicarboximide (MBTD), a benzothioxanthene derivative, as a reference for fluorescence ratiometric measurement. To prevent leakage of the dyes, both were photocopolymerized with acrylamide, hydroxyethyl methacrylate, and triethylene glycol dimethacrylate on the silanized glass surface. The reproducibility and response time of the prepared sensor were sufficient. Most common coexisting inorganic ions and organic compounds did not interfere with pH sensing. In the acidic pH range from 1.5 to 5.0 the fluorescence intensity ratio of the two dyes varied linearly as a function of pH. The sensing membrane was found to have a lifetime of at least one month. The sensor was applied to the analysis of waste water and artificial samples.     

Gallium tris­(iodate), Ga(IO3)3

Ga(IO₃)₃ crystallizes in the space group P6₃, with the Ga atom at a site with imposed threefold symmetry. The crystal structure consists of slightly distorted GaO₆ octa­hedra that are bridged by I atoms of IO₃⁻ groups, giving rise to a three‐dimensional polar network. The framework contains unoccupied hexa­gonal channels running parallel to the hexa­gonal [001] direction. The iodate groups have their stereochemically active non‐bonded electron pairs pointing in the same direction along [001], which creates the polarity in the structure. The I—O bond distances and O—I—O angles are normal, being in the ranges 1.783 (3)–1.847 (2) Å and 94.68 (11)–99.61 (12)°, respectively.     

硫化锌纳米粒子的乳液合成

纳米材料被人们认为是新型的功能材料^[1]。作为过渡金属硫化物,硫化锌（ZnS)材料显示出许多特异光电性能,在许多领域有着广泛的应用^[2],因而一直被应用和研究。     

Characterization of pore structure in metal-organic framework by small-angle X-ray scattering

MOF-5-like crystals were studied by small-angle X-ray scattering (SAXS) to reveal, both quantitatively and qualitatively, their real structural details, including pore surface characteristics, pore shape, size distribution, specific surface area (SSA), spatial distribution, and pore-network structure. A combined SAXS and wide-angle X-ray scattering (WAXS) experiment was conducted to investigate the variation of the pore structure with the MOF-5 crystalline phase produced at different cooling rates. The SSA of the MOF-5 crystals synthesized herein spanned a broad range from approximately 3100 to 800 m2/g. The real pore structures were divided into two regimes. In regime I the material consisted mainly of micropores of radius approximately 8 A as well as mesopores of radius 120 approximately 80 A. The structure in regime II was a fractal network of aggregated mesopores with radius >or=32 A as the monomer, reducing SSA and hydrogen uptake capacity at room temperature. The two regimes can be manipulated by controlling the synthesis parameters. The concurrent evolution of pore structure and crystalline phase during heating for solvent removal was also revealed by the in-situ SAXS/WAXS measurement. The understanding of the impact of the real pore structure on the properties is important to establish a favorable synthetic approach for markedly improving the hydrogen storage capacity of MOF-5.     

Construction and deconstruction of multilayer films containing polycarboxybetaine: effect of pH and ionic strength

The influences of pH and NaCl concentration of dipping solutions and the pH and NaCl concentration of disintegration solutions on the disintegration behaviors of poly(4-vinylpyridiniomethanecarboxylate) (PVPMC)/poly(sodium 4-styrenesulfonate) (PSS) (PVPMC/PSS) multilayer films were investigated by ultraviolet-visible spectroscopy (UV-vis), Fourier transform infrared spectroscopy (FT-IR), quartz crystal microbalance (QCM) and atomic force microscopy (AFM). It was found that the disintegration rates and degrees of PVPMC/PSS multilayer films in neutral water could be well controlled by changing pH of dipping solutions and immersion time during the disintegration process. Furthermore, PVPMC/PSS multilayer films could be disintegrated completely and rapidly in pH 8 alkali solution or physiological condition (i.e., 0.15 M NaCl solution). The controllable disintegration of PVPMC/PSS multilayer films was then utilized to fabricate PEC/PSS free-standing multilayer films, in which PEC was a positively charged polyelectrolyte complex made from excessive poly(diallyldimethylammonium) (PDDA) and PSS. The experimental results indicated that the disintegration rates of PVPMC/PSS sacrificial sublayer strongly affected the integrity of the resultant PEC/PSS free-standing multilayer films. Only free-floating PEC/PSS was released from neutral water by disintegrating PVPMC/PSS multilayer sublayers. However, large size flat and tube-like PEC/PSS free-standing multilayer films with good mechanical properties were obtained facilely from pH 8 alkali solution and 0.15 M NaCl solution, respectively. The preparation of such free-standing films at physiological condition may be useful in the biological or medical application.