Uniformly third-order accurate TVNE interpolations

In this paper, we develop an approximation procedure for functionsof bounded variations. Our procedure cannot increase the variationof the function being approximated, and also avoids discontinuityof the interpolation function.     

Matrix model in a class of time dependent supersymmetric backgrounds

We discuss the matrix model in a class of 11D time dependent supersymmetric backgrounds as obtained in [B. Chen, Phys. Lett. B 632 (2006) 393, hep-th/0508191]. We construct the matrix model action through the matrix regularization of the membrane action in the background. We show that the action is exact to all orders of fermionic coordinates. Furthermore we discuss the fuzzy sphere solutions in this background.     

堵塞效应与“全同带”的微观机制

利用处理推转壳模型的改进了的粒子数守恒方法(严格计及堵塞效应),对原子核的转动惯量进行了计算,计算中无任何自由参数,所得转动惯量(包括¹⁷⁰Yb,¹⁷¹Lu¹⁷¹Yb各转动带)及其奇偶差,与实验非常符合,转动惯量的奇偶差灵敏地依赖于被堵塞的能级位置及其对Coriolis力的响应。     

多项式理想准素分解的算法

讨论了多项式理想准素分解的算法,对于理想坐标变换中关键的“一般位置”的计算,给出了一个确定算法,并建立了特别规范Groebner基的概念,利用这一概念及文中提供的相应算法,可以方便地计算理想的维数,进而使用降维的方法来得到高维理想的准素分解。     

Crystallographic report: Crystal structure of tetra(4‐methyl‐5‐imidazole‐carboxyaldehyde)zinc(II) diperchlorate

The central zinc(II) atom in the title complex is tetrahedrally coordinated by four nitrogen atoms derived from 4‐methyl‐5‐imidazolecarboxyaldehyde ligands with Zn? N in the range 2.007(3) to 2.026(4) Å. Copyright © 2003 John Wiley & Sons, Ltd.     

晶格反演的嵌入原子法模型及其应用

讨论一种基于晶格反演的嵌入原子法模型 ,其特点是未知函数的参数化是对原子间对势和单原子电荷密度函数的晶格和 ,而不是对原子间对势和单个原子的电荷密度函数进行的 ,其最大优点在于待定参数可以用物理输入解析地表达出来 ,而不是像大多数埋入原子法模型中那样通过拟合来确定 .给出了它在计算点缺陷 (自间隙杂质和空位原子 )和晶体表面形成能方面的应用 .     

A highly sensitive and rapid assay for protein determination in human urine and penicillin using a Rayleigh light-scattering technique with benzeneazo-8-acetylamino-1-naphthol-3,6-disulfonic acid sodium salt.

A simple and sensitive method was conducted for the determination of trace amounts of proteins with benzeneazo-8-acetylamino-1-naphthol-3,6-disulfonic acid sodium salt (azophloxine, AP) using a Rayleigh light-scattering (RLS) technique. At pH 2.60 and in the presence of an emulsifier OP microemulsion, the RLS of AP can be greatly enhanced by proteins, owing to the interaction between AP and protein. The enhanced intensity is proportional to the concentration of proteins. Four proteins, including bovine serum albumin (BSA), human serum albumin (HSA), lysozyme (Lys) and gamma globulin (gamma-G) have been tested. For example, the linear range of BSA was 0 - 0.06 microg mL(-1) with detection limits of 2.38 ng mL(-1). The method was applied to the analysis of protein in human urine and penicillin samples with satisfactory results. The relative standard deviation was in all instances less than 4.0%, and the recovery was in the range of 97.5 - 104%.     

Coordination Sorption of Urea by Novel Urea Sorbent——Polymer-bound Metal Complexes

Urea can be sorbed by coordination (or complexation)with transitional metalpolyacrylic acid complex and transitional metal-polyacrylamide containing polyethylenepolyamine ligand complexes. The experimental results indicate that the sorbents can sorb about 60mg urea per gram of sorbent at 37℃ and the concentration of urea was 1300.0rag/1 in NaH_2PO_4 and Na_2HPO_4 buffer solution (pH=7.0) and the urea sorption capacity was affected by many factors such as other competive ligands, sorption time, pH and the concentration of urea.     

Mixed-valent diruthenium diphosphonate with kagomé structure

This paper reports the first example of diruthenium phosphonate with kagomé structure, namely, [NH3(CH2)4NH3][Ru2(hedpH(0.5))2].2H2O (hedp = 1-hydroxyethylidenediphosphonate). The compound contains kagomé layers that are linked by very strong hydrogen bonds into a nanoscale kagomé structure. Ferromagnetic interactions are mediated between the paramagnetic diruthenium units.     

Asymmetric synthesis of cis-5-tert-butylproline with metal carbenoid NH insertion

The highly stereoselective intramolecular metal carbenoid insertion reaction of sulfinimine-derived delta-amino alpha-diazoesters is used to prepare cis-5-tert-butylproline. A concerted or nearly concerted metal carbenoid N-H insertion reaction mechanism is proposed.