Template atom transfer radical polymerization of a diaminopyrimidine‐derivatized monomer in the presence of a uracil‐containing polymer

Uracil‐derivatized monomer 6‐undecyl‐1‐(4‐vinylbenzyl)uracil and diaminopyrimidine‐derivatized monomer 2,6‐dioctanoylamido‐4‐methacryloyloxypyrimidine (DMP) were synthesized and polymerized by atom transfer radical polymerization (ATRP). A well‐defined, highly soluble, uracil‐containing polymer, poly[6‐undecyl‐1‐(4‐vinylbenzyl)uracil] (PUVU), was prepared in dioxane at 90 °C with CuBr/1,1,4,7,10,10‐hexamethyltriethylenetetramine as the catalyst and methyl α‐bromophenylacetate as the initiator. PUVU was further used as a template for the ATRP of DMP. The enhanced apparent rate constant of the DMP polymerization in the presence of PUVU indicated that the ATRP of DMP occurred along the PUVU template. The template polymerization produced a stable and insoluble macromolecular complex, PUVU/poly(2,6‐dioctanoylamido‐4‐methacryloyloxypyrimidine). An X‐ray diffraction study confirmed that the complex had strandlike domains. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6607–6615, 2006     

Chiral separation of synthetic vicinal diol compounds by capillary zone electrophoresis with borate buffer and beta-cyclodextrin as buffer additive.

The investigation on capillary electrophoretic enantioseparation of six synthetic compounds containing vicinal diol groups has been undertaken to acquire the optimum conditions using native beta-cyclodextrin (beta-CD) as chiral selector and borate as a background electrolyte. The separation was carried out in an uncoated capillary (58.5 cm x 75 microm i.d., effective length 48.5 cm) and the effects of several important factors were investigated in detail. The results showed that beta-CD as a chiral selector exhibited good enantioselectivity and that the enantioseparation was greatly influenced by the structure of the diols, the borate concentration and the buffer pH. The optimum performance was obtained for the chiral vicinal diols under the conditions of 200 mM borate buffer of pH 9.8 containing 1.7% beta-CD at an applied voltage of 15 kV and a capillary temperature of 20 degrees C. Under the conditions, four diols were baseline separated with fast analysis time and the good theoretical plate numbers (above 10 x 10(4)) and favorable migration-time reproducibilities (RSDs below 3.0%) were obtained. The separation results were satisfactory.     

浅析加强英语听说能力的培养--从CET改革谈起

交际是学习语言的最终目的.大学英语四、六级考试改革突出了英语听说能力,其目的是促进学生重视英语交际能力.要提高学生英语交际能力,在英语教学中教师应正确处理好几对关系:听与说的关系;交际文化与语言文化的关系;教师与学生的关系;准确与流利的关系等,把握教学原则,从而加强学生的听说能力培养.     

锻炼对老年人肺通气功能影响的研究

本文采用电子肺活量计对218名老人进行了肺通气功能的测试。测试结果表明:体育锻炼对老年人肺通气功能有良好影响。本文为老年人肺通气功能的研究、评价及老年人体育运动的研究提供了实验性依据。     

Some existence results on periodic and generalized periodic solutions for singular hamiltonian systems

In this paper, we use the variational method to study the existence of periodic and generalized periodic solutions of planar second order Hamiltonian systems when a singular potential is present. The results obtained are applied to the study of generalized periodic solutions of the Restricted Three-Body Problem and the Planarn-Body Problem.     

气相法制备N－乙基苯胺催化剂的研究进展

对苯胺、乙醇气相Ｎ－乙基化反应催化剂的制备及其活性进行了评述，特别是对近十年来的发展作出了较详细而深入的论述，指出研制这类反应催化剂的重要性和今后的发展方向。     

Asymmetric synthesis XXVII: Asymmetric catalytic trimethylsilylcyanation of aldehydes by novel Ti-chiral Schiff base complexes

Enantioselective catalytic trimethylsilylcyanations of aldehydes with 48% to 92% e.e. have been studied using the novel Ti-chiral Schiff base complexes. We have found that the catalyst led to high enantoselectivity when the molar ratio of the Schiff base 1 to Ti(O-i-Pr)₄ was 2:1.     

粘结平面对称分叉裂纹的奇异积分方程数值解

本文对一个含分叉裂纹的弹性半平面与另一不同材料的半平面粘结的问题用复势方法化为一组三个复Caucby型奇异积分方程。采用修正的Gauss-Legendre和修正的Lobatto-Legendre数值求积法则化成一代数方程组,裂纹尖端的应力强度因子值可从代数方程组的解求得。本文计算得到了弹性半平面、刚体与弹性半平面相粘结、两种不同材料的弹性半平面相粘结的三种问题的几种几何形状的对称分叉裂纹的应力强度因子。本文的结果扩充了“应力强度因子手册”的内容。     

Molar conductivity calculation of Li-ion battery electrolyte based on mode coupling theory

A method is proposed to calculate molar conductivity based on mode coupling theory in which the ion transference number is introduced into the theory. The molar conductivities of LiPF6, LiClO4, LiBF4, LiAsF6 in PC (propylene carbonate) are calculated based on this method. The results fit well to the literature data. This presents a potential way to calculate the conductivities of Li-ion battery electrolytes.