非均匀磁场中（1／2，1）混合自旋海森堡XXZ模型的热纠缠

研究在非均匀磁场作用下的两混合自旋（1／2，1）各向异性海森堡XXZ模型的热纠缠特性．在均匀磁场下，随着各向异性参数的增加，临界磁场和临界温度都增大．在非均匀磁场体系中磁场不均匀度在提高纠缠的临界温度和扩大纠缠存在的范围方面起着很重要的作用．     

图T1,1,m与Q(3,n)中有路因子的充分必要条件及T1,1,m的匹配等价类

如果一个图的匹配多项式可以被一个路的匹配多项式整除,我们就称此路是该图的一个路因子,路因子在刻画图的匹配等价类,研究匹配唯一性方面有很重要的作用.本文得到了图T1,1.m与图Q(3,n)中有路因子的充分必要条件.     

植物中钙解码机制的研究进展

Ca2＋作为重要的第二信使,在植物生长发育中起着非常重要的作用．目前已经鉴定的植物Ca2＋传感器蛋白有：钙调素（CaM）、类钙调素蛋白（CMLs）、钙依赖型蛋白激酶（CDPKs）和类钙调磷酸酶B亚基蛋白（CBLs）及其互作蛋白激酶（CIPKs）,这些传感器蛋白多以基因家族形式存在,并且在植物中能够形成错综复杂的钙离子信号传递网络系统．主要从植物Ca2＋传感器蛋白的生化特性、生理功能和靶蛋白3个方面,综述了植物解码钙信号机制的最新研究进展．     

Grotzsch图的匹配等价图

文章研究了Grotzsch图的一些性质,以及它的匹配等价图.     

含聚碳酸酯,4—羟基苯甲酸,己二醇和1,4—苯二甲酸结构的嵌段共聚物的…

以端酰氯基因的热致液晶共聚酯ＨＴＨ－６和端酚羟基的聚碳酸酯齐聚物为原料，通过溶液缩聚法制备了含ＰＣ和ＨＴＨ－６的嵌段共聚物，并用ＩＲ、ＰＯＭ、ＤＳＣ、ＷＡＸＤ等手段对共聚物结构，热行为和结晶行为进了表征。ＤＳＣ和ＰＯＭ结果证明这些嵌段共聚物都属向列型热致性液晶。在２８０℃以睛的温度范围内无相分离，而在较高温度为两相结构，共聚物的结晶结构与ＨＴＨ－６相同，结晶度随ＨＴＨ－６含量增加而增加，结晶速度也     

无柔性间隔基侧链型液晶高分子复合定形相变材料的制备与性能研究

设计合成了一系列具有不同烷氧基尾链长度的单体4′-烷氧基-4-联苯酚甲基丙烯酸酯Mbi Cm(m=1,2,4,6,8,10,12,14,16,18),通过自由基聚合方法合成了相应的具有不同烷氧基尾链长度的无柔性间隔基侧链型液晶高分子PMbi Cm,将所得的侧链型液晶高分子和相变材料石蜡按一定质量比混合,通过"加热-冷却法"成功制备了定形相变材料.通过凝胶测试发现当尾链长度为m=12,14,16,18时,高分子对固体石蜡具有良好的凝胶定形效果,且随着烷氧基尾链的增长,聚合物和石蜡的相容性增加,最低凝胶浓度降低,得到定形相变材料的凝胶解缔温度也相应下降.通过示差扫描量热法(DSC)、热重分析法(TG)、流变(Rheology)等测试考察了定形相变材料的相变储能性能、热稳定性和流变性能,实验结果表明该定形相变材料具有相变焓值高、热稳定性好、凝胶强度高等优点.通过红外光谱(FTIR)、偏光显微镜(POM)和扫描电镜(SEM)等测试发现PMbi Cm通过非共价键作用力自聚集形成三维凝胶网络结构,对石蜡起固定支撑作用.     

树枝状偶氮液晶高分子(PAMAM-MMAZO)的合成及表征

树枝状偶氮液晶高分子(PAMAM-MMAZO)的合成及表征;树枝状聚酰胺-胺;树枝状偶氮液晶;表面修饰;液晶性     

关于路与圈的匹配多项式的一个注记（英文）

The spectra of matching polynomials which are useful in the computations of resonance energy and grand canonical partition functions of molecular's. It also present other properties for certain classes of graphs and lattices. In [1] Balasubramanian calculates several matching polynomials and matching roots of several molecular graphs. He found that the matching polynomial of C_6, C_(10), C_(14), C_(18) and C_(22) are divided by x~2-2. In this note,we prove that x~2-2 divides MC_(4k+2)(x), k = 1, 2,..., n and obtain some other properties of matching polynomials of paths and cycles.     

Synthesis and liquid crystalline behavior of side chain liquid crystalline polymers containing triphenylene discotic mesogens with different length flexible spacers

A series of side chain liquid crystalline polymers(SCLCPs) containing triphenylene(Tp) units in the side chains, denoted as PMTS(without spacer) and PMTn S(n = 2, 3, 4, 6, which is the number of the methylene units between the main chain and Tp moieties in the side chains), with different lengths of spacers were synthesized through conventional free radical polymerization. The chemical structures of the monomers were confirmed by 1H/13C-NMR, and the phase behaviors were examined by differential scanning calorimetry(DSC), polarized optical microscopy(POM) and wide-angle X-ray diffraction(1D and 2D WAXD). The molecular characterization of the polymers was performed with 1H-NMR, gel permeation chromatography(GPC) and thermogravimetric analysis(TGA). The phase behaviors of the polymers have been investigated by a combination of techniques including DSC, POM, 1D and 2D WAXD. The results showed that the length of spacer has significant effects on the LC phase behavior of polymers. For PMTS and PMT2 S, they displayed the columnar phase developed by the Tp moieties and the main chain as a whole due to the strong coupling effect of the Tp moieties and the main chain. For the PMT3 S, PMT4 S and PMT6 S, they formed the symmetry hexagonal columnar(ΦH) phase owing to the decoupling effect. All of these indicated that the "decoupling effect" or "coupling effect" depended on the length of spacers, leading to the different LC phase formation mechanism.