用倒相换能器抑制声表面波谐振滤波器的直达讯号

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A Problem in Applied Topology: on the Selection of Cycles for the Flexibility Analysis of Skeletal Structures

A theory of generalized statical bases is developed for usein the flexibility methods as applied to skeletal structuralproblems. It is shown that any maximal linearly independentset of cycles of the integral cycle group of a linear graphmodel of the structure may be used in the formation of a staticalbasis. Such a set of simple cycles is found by embedding thisgraph into a two-dimensional polyhedron. Cell complexes areformed so that the simple cycles bounding the 2-cells correspondto substructures on which a statical basis may be constructed.Two methods are given for the construction of the embeddings.In one a collapsible complex is formed from a union of a setof disks; while in the other the embedding is into an orientablemanifold which is modified to form an admissible complex.     

额尔齐斯河（新疆段）水质评价

对额尔齐斯河1993～1999年的水质污染数据用因子分析的方法进行分析,得到评价额尔齐斯河水质污染的有机污染因子,综合污染因子和金属污染因子,并以此对额尔齐斯河水质污染情况作出较客观的评价。     

向量随机测度关于白噪声的积分的收敛性

本文主要讨论s.i.s.向量随机测度关于白噪声的积分的收敛性,我们得到了如下结果设X是具type2的Banach空间,{Fn}∞n=0是一列被μ所控制的X值s.i.s随机测度,对任意的E∈∑,E[Fn(E)]=0,E‖Fn(E)‖2＜+∞,{Fn(E)}∞n=0是一致W弱可积,且{Fn}∞n=1弱几乎收敛到F0,则(1)对每个n≥0∫FndW是s.i.s向量随机测度;(2)∫FndWwp→∫F0dW.     

Investigation of internal and external potentials acting on benzyl halides dissolved in different nematic solvents

(Molecular Physics, 1994, 83, 309–326)     

ON THE IMPULSIVE BEVERTON–HOLT EQUATION AND EXTINCTION CONDITIONS IN POPULATION DYNAMICS

Abstract This paper is devoted to investigate extinction and nonextinction conditions of the extended Beverton–Holt equation (BHE) for dynamics of populations in Ecology when potential discontinuities at sampling points are included in the model. The proposed model is described by means of four sequences of parameters. Two of them are the intrinsic growth rate and the carrying capacity sequences which are included in the basic BHE model. The other two ones, namely, the harvesting (i.e., the hunting or fishing quota) and the internal consumption (which can include positive and negative migrations in the considered population habitat) sequences are included to parameterize the model discontinuities. Such discontinuities are related to impulses in the corresponding continuous‐time logistic equation. The obtained results establish how the harvesting quota and/or the internal consumption has to be fixed to guarantee the population nonextinction or, eventually, its extinction. Finally, some controllability results related to the search of a carrying capacity sequence such that the solution of the proposed impulsive BHE tracks a reference one are obtained.     

PAINT-ing Fluorenylmethoxycarbonyl (Fmoc)-Diphenylalanine Hydrogels

Self-assembly of fluorenylmethoxycarbonyl-protected diphenylalanine (FmocFF) in water is widely known to produce hydrogels. Typically, confocal microscopy is used to visualize such hydrogels under wet conditions, that is, without freezing or drying. However, key aspects of hydrogels like fiber diameter, network morphology and mesh size are sub-diffraction limited features and cannot be visualized effectively using this approach. In this work, we show that it is possible to image FmocFF hydrogels by Points Accumulation for Imaging in Nanoscale Topography (PAINT) in native conditions and without direct gel labelling. We demonstrate that the fiber network can be visualized with improved resolution (≈50 nm) both in 2D and 3D. Quantitative information is extracted such as mesh size and fiber diameter. This method can complement the existing characterization tools for hydrogels and provide useful information supporting the design of new materials.     

CaF2：xYb3+, yEr3+纳米颗粒的合成及其上转换发光性质

采用水热合成法制备了CaF₂：xYb³⁺,yEr³⁺（x=0.1~0.8,y=0.01~0.08）纳米颗粒,利用X射线粉末衍射仪、透射电子显微镜和F-4600荧光分光光度计表征了样品的物相和形貌尺寸,并探究了Yb³⁺和Er³⁺掺杂浓度对样品的上转换发光性质的影响。结果表明,所合成的样品为立方相,球形颗粒,平均直径为 12 nm,敏化剂Yb³⁺的最佳掺杂摩尔分数为20%,而激活剂Er³⁺的最佳掺杂摩尔分数为6%。此时,绿光与红光的强度之比最大。     

Structure–Property Relationships and 1O2 Photosensitisation in Sterically Encumbered Diimine PtII Acetylide Complexes

A series of sterically encumbered [Pt( L )(σ‐acetylide)₂] complexes were prepared in which L , a dendritic polyaromatic diimine ligand, was held constant ( L =1‐(2,2′‐bipyrid‐6‐yl)‐2,3,4,5‐tetrakis(4‐tert‐butylphenyl)benzene) and the cis ethynyl co‐ligands were varied. The optical properties of the complexes were tuned by changing the electronic character, extent of π conjugation and steric bulk of the ethynyl ligands. Replacing electron‐withdrawing phenyl‐CF₃ substituents ( 4 ) with electron‐donating pyrenes ( 5 ) resulted in a red shift of both the lowest‐energy absorption (ΔE=3300 cm^?1, 61 nm) and emission bands (ΔE=1930 cm^?1, 64 nm). The emission, assigned in each case as phosphorescence on the basis of the excited‐state lifetimes, switched from being ³MMLL′CT‐derived (mixed metal–ligand‐to‐ligand charge transfer) when phenyl/polyphenylene substituents ( 3 , 4 , 6 ) were present, to ligand‐centred ³ππ* when the substituents were more conjugated aromatic platforms [pyrene ( 5 ) or hexa‐peri‐hexabenzocoronene ( 7 )]. The novel Pt^II acetylide complexes 5 and 7 absorb strongly in the visible region of the electromagnetic spectrum, which along with their long triplet excited‐state lifetimes suggested they would be good candidates for use as singlet‐oxygen photosensitisers. Determined by in situ photooxidation of 1,5‐dihydroxynaphthalene (DHN), the photooxidation rate with pyrenyl‐ 5 as sensitiser (k_obs=39.3×10^?3 min^?1) was over half that of the known ¹O₂ sensitiser tetraphenylporphyrin (k_obs=78.6×10^?3 min^?1) under the same conditions. Measured ¹O₂ quantum yields of complexes 5 and 7 were half and one‐third, respectively, of that of TPP, and thus reveal an efficient triplet–triplet energy‐transfer process in both cases.