基于PWLAN GPF的QoS性能分析与仿真

基于IEEE802.11协议中PCF/DCF技术,在无线局域网(WLAN)中,介绍了GPF的系统结构和数据帧格式等。分别对基于IEEE802.11b媒体接入控制(MAC)协议、基于IEEE802.11e媒体接入控制(MAC)协议以及基于业务划分Qos的GPF仿真的时间参数和接入原则等进行了说明。在PWLAN的3种测试环境下,对802.11b、802.11e、GPF协议的整体性能进行了仿真,并对其结果进行了分析。     

Synthesis,Characterization and Crystal Structure of Ln(CCl_3COO)_3·(phen)_2·2H_2O

Coordination compounds of lanthanide trichloroacetates with 1,10-phenanthroline weresynthesized and characterized as Ln(CCl_3COO)_3·(phen)_2·2H_2O(phen=1,10-phenanthroline,Ln=Tb～Lu)by chemical analysis,IR spectra,thermal analysis and crystal X-ray structural analysis.The crystal ofEr(CCl_3COO)_3·(phen)_2·2H_2O belongs to monoclinic system,with space group P2_1/c,a=1.6969(6)nm,b=1.3776(5)nm,c=1.7563(9)nm,β=114.79(9)°,V=3.727(1)nm~3,Z=4.     

SiP协调设计和PI解析(6)

概述了SiP(系统封装)协调设计和PI解析:(1)协调工程(下);(2)电源供给电路;(3)SSD噪声;(4)旁路电容。     

Calculation of the ligand–lanthanide ion energy transfer rate in coordination compounds: contributions of exchange interactions

Recently, one of us (O.L.M.) developed a theoretical approach to the energy transfer process between a ligand and a lanthanide ion in luminescent compounds. This approach takes into account the direct Coulomb interaction only. Here we present further calculations which also include the exchange Coulomb interaction (isotropic and anisotropic). The selection rules on the total angular momentum, J, of the lanthanide 4f states, derived from each interaction are different. They are in fact complementary. We discuss the case of energy transfer to the ⁵D₁ manifold of the Eu³⁺ ion, which is forbidden when only the direct Coulomb interaction is considered but becomes allowed through the exchange interaction. In this case numerical estimates show that, depending on resonance conditions and the nature of the ligand donor state, the transfer rate may assume very high values. It is also emphasised that, according to the present approach, energy transfer to the ⁵D₀ level of the Eu³⁺ ion is forbidden by both mechanisms, provided J-mixing between the ⁷F₀ and ⁷F₂ manifolds is neglected.     

A novel stair-like lithium coordination polymer constructed from 4,4′-bipyridine

A novel stair-like lithium coordination polymer Li₂(4,4′-bpy)₂(NO₃)₂, 1, has been synthesized by using standard Schlenk techniques. X-ray diffraction shows the 2D stair-like framework contains an approximately perpendicular 1D “Z” type Li-4,4′-bpy chain and an unprecedented Li–NO₃ chain.     

Coordination-induced formation of nanobelts of organic-inorganic hybrid materials at room temperature

The unexpected finding that the direct mix of o-phenylenediamine and H₂PdCl₄ aqueous solution at room temperature leads to supramolecular nanobelts of coordination polymers was reported. The morphology of the structures was characterized by scanning electron microscopy (SEM) and the chemical composition was examined by energy-dispersed spectrum (EDS) and X-ray maps analysis. The possible formation process of such supramolecular nanobelts is given and the influence of the molar ratio of reactants on the formation of these nanobelts is also examined. It is also found that the molar ratio of reactants has strong influence on the formation of the supramolecular structures.     

Novel Cd(II) and Co(II) 2-D frameworks based on terephthalate and 1-substitutedimidazole mixed-ligands

The two Cd(II) and Co(II) 2-D frameworks have been prepared by means of self-assemblies of Cd(II) or Co(II) salts and 1-substituted imidazole and terephthalic acid, and structurally characterized by X-ray diffraction analyses. In complex 1 2-D frameworks with rhombic cavity are formed, in which the each top point of rhombus contains one hexa and two heptacoordinated Cd(II). In complex 2 2-D networks with rectangular cavities are formed, and the opposite benzene rings from carboxyls in each rectangular cavity are parallel.     

Near-infrared photodetection with a diruthenium complex having redox-switchable wavelength response

We report on the electrochromic behavior of a dinuclear ruthenium complex, which provides high environmental stability together with an intense absorption maximum at 1237 nm in solution in its +3 oxidation state. To verify its optoelectronic properties, we used this complex as the photoactive material in a planar photodetector prototype for near-infrared light pulses, succeeding in the detection of a train of light pulses at a wavelength of 1280 nm.     

Synthesis and catalytic properties of a new window type hybrid porous zirconium phosphonate

An organic–inorganic hybrid zirconium phosphonate (noted as ZrNCP) with window type porous structure was synthesized by using β–alanine–N,N-dimethylidenephosphonic acid and zirconium dichloride oxide octahydrate. The sample possesses regular flake morphology, and these flakes have porous framework structure, which were characterized by SEM, HRTEM, N₂ sorption, XRD, TGA–DSC, elemental analysis, XPS, and FT-IR spectroscopy techniques. The as-prepared ZrNCP can be used as catalyst to oxidation of formaldehyde after Fe³⁺ was intercalated and coordinated with nitrogen and carbonyl groups inside the porous walls of ZrNCP. 90.1% of oxidized efficiency was obtained when the catalyst was added into formaldehyde solution (40% water solution) at 80 °C.