Anomaly in the charge radii and nuclear structure

The axially deformed relativistic mean field theory is applied to study the isotope shift of charge distributions of odd-Z Pr isotope chain. The nuclear structure associated with the shell and the isotope effect is investigated. The mechanism of link in the isotope shift at the neutron magic number N = 82 is revealed to be dependent on the neutron energy level structure at the Fermi energy, demonstrating that the spin-orbit coupling interaction and p-n attraction are well described by the relativistic mean field theory.

参与肿瘤侵袭和转移的细胞外基质降解酶

肿瘤细胞在侵袭和转移过程中必需穿透一系列天然组织屏障—基底膜和细胞外基质。合成及分泌大量基质降解酶，降解细胞外基质是肿瘤细胞侵袭、转移的重要步骤［１］。目前所知与肿瘤侵袭、转移有关的基质降解酶有两大类：蛋白酶类和糖苷酶类，前者主要降解细胞外基质中的蛋...

颗粒有机质的来源、测定及其影响因素

土壤活性有机质及其组分作为土壤质量的重要指标在土壤化学、物理和生物性质方面起着重要作用。颗粒有机质能够有效地反映有机质的特性,与微生物生长、营养供给及C、N的生物学调节密切相关。作为活性有机质的一个量度指标,颗粒有机质越来越受到人们的重视。本文综述了土壤颗粒有机质的来源及其在土壤有机质转化过程中的作用,对其测定方法作了系统的描述,阐明了土壤理化性质、农业措施(施肥与耕作)及土地利用类型对土壤颗粒有机质在土壤形成及维持其稳定性方面的影响。

岷江上游干旱河谷农林边界影响域的研究

对岷江上游农林边界的影响域进行研究 ,以提高该区管理农田和林地的水平 .共调查 3种类型农林边界 10条样带 ,采用移动窗口法对植物多样性的数据进行分析 ,结果表明 ,当窗口宽度达到 6～ 10时 ,SED曲线的变化趋向稳定 ,并且在曲线上有一或两个峰值出现 .不同类型边界的影响域是不同的 ,但均在距边界 5 0m内 .各类型边界的影响域多在 12～ 30m之间 .6条林地样带只有M 2和M6样带林地的影响域被确定 ,而 4条农田样带的影响域均被确定 .影响域的大小取决于边界两侧斑块类型和地形以及小气候等因子 ,但坡向对其影响不大 ;移动窗口法能有效地刻画边界动态 ,是一种分析边界简单而有力的工具 .这些结果有利于进一步理解干旱河谷区农林间的相互作用 .

1,2,3,4-Alternate double cone conformational extreme in the supramolecular assemblies of p-sulfonatocalix[8]arene

Two supramolecular assemblies of p-sulfonato-calix[8]arene were stacked by some infinite 1D 'molecular capsule' chains in which the calixarenes adopt an unprecedented 1,2,3,4-alternate double cone conformation.

Chain propagation kinetics on melt grafting reaction

Graft copolymerization in the molten state is of fundamental importance as a probe of chemical modification and reactive compatibilization. However, few grafting kinetic studies on reactive extrusion have been carried out because of the inherent difficulties, as expected. In this work, we have studied chain propagation kinetics on melt grafting using pre-irradiated linear low density polyethylene (LLDPE) and three monomers, acrylic acid (AA), methacrylic acid (MAA), and methyl methacrylate (MMA), as the model system. We measured the apparent chain propagation rate coefficients of grafting (k(p,g)) and homopolymerization (k(p,h)) at an initial stage for the melt grafting by FT-IR spectroscopy and electron spin resonance spectroscopy. It was observed that the convective mixing affected the rate coefficients. The magnitude of k(p,h) and k(p,g) were in the same order, but k(p,h) was slightly larger than k(p,g) The k(p,g) of the three grafting systems increased in the order: LLDPE/MMA < LLDPE/MAA < LLDPE/AA. These results are explained in terms of phase separation, solubility, and inherent reactivity of the monomer.

Synthesis and characterization of novel polythiophenes containing poly(ethylene oxide) side chains

Thiophene copolymers and their derivatives with poly(ethylene oxide) side chains were synthesized. The starting monomers were 3-hexylthiophene and 2-(3-thienyl) ethanol with poly(ethylene oxide) grafted to the side chains. New functionalized polythiophenes were prepared by both chemical oxidation with FeCl3 and electropolymerization. The conjugating polymers were characterized. The structures of the polythiophene derivatives agreed with the design.

Copolymerization of carbon dioxide and propylene oxide with neodymium trichloroacetate-based coordination catalyst

The copolymerizations of carbon dioxide (CO2) and propylene oxide (PO) were performed using new ternary rare-earth catalyst, It was found that the rare-earth coordination catalyst consisting of Nd(CCl3COO)(3), ZnEt2 and glycerine was very effective for the copolymerization of PO with CO2. The effects of the relative molar ratio and addition order of the catalyst components, copolymerization reaction time, and operating pressure as well as temperature on the copolymerization were systematically investigated. At an appropriate combination of all variables, the yield could be as high as 6875 g/mol Nd per hour at 90 degreesC in a 8 h reaction period.

Sodium ion transfer across micro water/1,2-DCE interface facilitated by liquid crystal crown ether

The sodium ion transfer across the micro-water/1,2-dichloroethane interface facilitated by a novel ionophore, liquid crystal crown ether was studied systematically. The sodium ion transfer facilitated by LCCE is controlled by diffusion studied by cyclic voltammetry. The diffusion coefficient of LCCE in 1,2-dichloroethane was calculated to be equal to (2.61 +/- 0.12) X 10(-6) cm(2)/s and the stability constant of the complex between Na+ and LCCE was determined as lg beta (o) = 5.7 in 1,2-dichloroethane.

端烯基液晶冠醚推动钠离子在微液/液界面的转移

用循环伏安法研究新型载体端烯基液晶冠醚推动钠离子的转移 ,结果表明 ,钠离子的转移由扩散控制 .探讨了影响钠离子转移的因素 ,如端烯基液晶冠醚和钠离子的浓度等 .求算出端烯基液晶冠醚在 1 ,2 -二氯乙烷中的扩散系数为 ( 2 .6 1± 0 .1 2 )× 1 0 - 6cm2 /s,端烯基液晶冠醚和钠离子在 1 ,2 -二氯乙烷中所形成的配合物稳定常数 lgβo=5 .7

SYNTHESIS AND CRYSTAL-STRUCTURE OF [(ME4C2CP2SMCL.MGCL2.3THF)THF]2

[(Me4C2Cp2SmCl.MgCl2.3THF)THF]2 was prepared by the reaction of Me4C2Cp2MgCl2.4THF (Cp=C5H4, THF = tetrahydrofuran) with SmCl3 in THF. The crystals belong to triclinic space group P-1 with a 12.149(3), b 13.187(4), c 13.810(5) angstrom, alpha 117.23(2), beta 94.07(2), gamma 62.86(2)-degrees, V = 1723.9(1.0) angstrom3. In the molecular structure of the title compound there is a symmetrical centre and a quadrilateral formed by SM, Mg, Cl1, Cl2 atoms. Two centroids of the cyclopentadienyls, bridged by a tetramethylethano group form with three bridging chlorine atoms (Cl1, Cl2, Cl1a) a pseudo-trigonal bipyramid around Sm. Three oxygen atoms of THF and three chlorine atoMS (Cl1, Cl2, Cl3) constitute a distorted octahedron around Mg.