CuO-BaO/SiO2催化剂的结构表征

以XRD、XPS和EXAFS手段对CuO－BaO／Sic2催化剂及其还原态的结构进行了研究．结果表明，在CuO－BaO／SiO2体系中铜和钡都是以氧化态的形式存在，超细SiO2载体对所负载的CuO的结构有影响．随着样品负载量的逐渐降低，Cu－O和Cu－Cu睡的健长和配位数逐渐征小，而且低载量样品的健长和配位数减小的幅度最大．在总负载量＞13．39％的样品中，CuO以晶相的形式存在；总负载量＜13．39％的样品中，CUO呈现单层分布的高分出状态．还原态样品中钢以本价铜的形式存在，随负载量的降低，还原态Cu－Cu健的镇长和配位数也分别呈现出逐渐减小的趋势．还原态中心铜原子在催化剂表面的分布状态基本上保持了氧化态催化剂中CuO物相的分市状态．     

交替三线性分解算法与反相高效液相-二极管阵列检测方法相结合同时测定苯二酚的位置异构体

 利用交替三线性分解算法与反相高效液相 二极管阵列检测 (RP HPLC DAD)相结合 ,在洗脱时间为1 0 86min～ 1 399min(间隔 1 / 1 50min)、紫外吸收波长为 2 68nm～ 2 98nm(间隔 1nm)时对苯二酚位置异构体的重叠及光谱体系进行了分辨研究。分辨结果与实际结果一致。同时测定了水溶液中共存的邻苯二酚、间苯二酚和对苯二酚的含量 ,回收率分别为 (1 0 0 1± 1 0 ) % ,(99 4± 1 4) % ,(1 0 0 5± 1 7) %。研究结果表明 :该方法定量快速准确 ,实验操作步骤简单 ,解决了在干扰物存在条件下三者很难同时分辨的问题。     

Adaptive Constrained Control of Unknown Strict Feedback Nonlinear Systems With Dead Zone Input北大核心CSCD

研究了具有死区输入的预设约束未知高阶严格反馈非线性系统的控制问题,提出了一种基于免疫函数的自抗扰预设漏斗约束自适应控制策略。首先,针对系统内部的未知问题,采用免疫函数与扩张状态观测器结合对系统内部未知项进行观测;其次,通过Lyapunov方法与漏斗控制相结合设计控制器,使得跟踪误差能够维持在预先设定的漏斗约束范围内;同时,利用双曲正切函数速率变化快这一特性设计自适应控制律,引入指令滤波器避免反步法中重复求导问题,分析证明了闭环系统所有信号的有界性。仿真实例表明了控制方法的有效性。     

Matrix semigroups—generators and relations

Some presentations for the semigroups of all 2×2 matrices and all 2×2 matrices of determinant 0 or 1 over the field GF(p) (p prime) are given. In particular, if <a, b, c‖ R> is any (semigroup) presentation for the general linear group in terms of generators $$A = \left( {\begin{array}{*{20}c} 1 & 0 \\ 1 & 1 \\ \end{array} } \right),B = \left( {\begin{array}{*{20}c} 1 & 1 \\ 0 & 1 \\ \end{array} } \right),C = \left( {\begin{array}{*{20}c} 1 & 0 \\ 0 & \xi \\ \end{array} } \right),$$ where ζ is a primitive root of 1 modulop, then the presentation $$\langle a,b,c,t|R,t^2 = ct = tc = t,tba^{p - 1} t = 0,b^{\xi - 1} atb = a^{\xi - 1} tb^\xi a^{1 - \xi - 1} \rangle $$ defines the semigroup of all 2×2 matrices over GF (2,p) in terms of generatorsA, B, C and $$T = \left( {\begin{array}{*{20}c} 1 & 0 \\ 0 & 0 \\ \end{array} } \right).$$ Generating sets and ranks of various matrix semigroups are also found.     

Crystal structures and voltammetric behavior of three copper(II) complexes derived from bulky Schiff bases

Three Schiff base copper(II) complexes have been prepared and characterized by elemental analysis, mass spectra, i.r., electronic spectra, _eff and X-ray crystal structures. Cyclic voltammetry studies on the complexes indicate a dependence of the cathodic potentials upon electronic effects, but independence on the solid state structure.     

Synthesis of Tetra—Schiff Base Macrocyclic Compound Containing Benzo—12—crown—4

Tetra-Schiff base macrocyclic compound containing benzo-12-crown-4 was synthesized via condensation of 2,6-diformyl-4-methyl-phenol with 4′，5′-diaminobenzo-12-C-4 promoted by proton. The compound was characterized by MS,IR ^1HNMR spectroscopy and elemental analysis.     

Investigation of Isomerization of 2—Seleno—1,3,2—diazaphospholidine Derivatives

For the first time the isomerization of 1,3,2-diazaphospholidine-2-sclenide dervatives in refluxing benzene in the presence of trace water was observed. The structures of isomerized products were determined by IR, ^1H NMR,^31P NMR, elemental analysis and X-ray crystallography. The mechanism of isomerization was also proposed.     

用计算模拟方法研究Al_3P_4O_(16)~(3-)计量比的二维层状磷酸铝中的有机胺模板能力

将快速 Monte Carlo方法与分子动力学方法相结合 ,研究了不同种类有机分子在 Al3P4 O3- 1 6 计量比的二维层状磷酸铝形成中的模板能力 .依据主 -客体之间非键相互作用能 (包括范德华能、氢键能和库仑能 ) ,可合理地解释已知实验现象 ,并能有效地预测出适于形成某一特定无机层结构的有机胺模板剂 .通过选择理论预测的有机胺分子作为模板剂 ,成功地合成了二维层状磷酸铝化合物 Al3P4 O1 6 · 1 .5 H3NC6 H1 0 NH3.     

Studium der Reduktion von Resazurin

Zusammenfassung In dieser Arbeit wurden Schlußfolgerungen über den simultanen Verlauf der beiden Reduktionsphasen von Resazurin überprüft.Weiters wurden Bedingungen für die quantitative titanometrische Bestimmung von Resazurin und seiner Derivate ermittelt.

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The conclusions about the simultaneous course of reduction of Resazurin to Resorufin and Resorufin to Dihidroresorufin were verified in this work.The conditions for the quantitative titanometric determination of Resazurin and its derivatives were found.

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Mit 4 Abbildungen     

新型手性双膦配体的合成及其催化性能考察

以苯乙烯为原料,通过Sharpless不对称二羟基化反应合成高对映体纯的苯基乙二醇,经环化、亲核开环和取代反应转化为手性碳膦-氧膦型双膦配体.后者与[Rh(COD)Cl]2及NH4PF6作用生成手性膦-铑阳离子催化剂.在α-脱氢氨基酸衍生物的不对称氢化反应中,化学转化率为100%,对映选择性最高达到77?.