The embedding method beyond the single-channel case

We investigate the relationship between persistent currents in multi-channel rings containing an embedded scatterer and the conductance through the same scatterer attached to leads. The case of two uncoupled channels corresponds to a Hubbard chain, for which the one-dimensional embedding method is readily generalized. Various tests are carried out to validate this new procedure, and the conductance of short one-dimensional Hubbard chains attached to perfect leads is computed for different system sizes and interaction strengths. In the case of two coupled channels the conductance can be obtained from a statistical analysis of the persistent current or by reducing the multi-channel scattering problem to several single-channel setups.     

新型电荷转移多金属氧酸盐的合成和红外光谱研究

以4种道森结构的杂多酸和3种芳香杂环化合物为原料合成了11种新型电荷转移多金属氧酸盐，研究了它们的红外光谱。结果表明：杂多酸形成电荷转移盐后，杂多阴离子的结构略有畸变但仍保持道森结构；有机给体和杂多阴离子之间存在电荷转移相互作用。     

一类亚解析函数的复合边值问题

本文研究了一类亚解析函数的复合边值问题.利用经典的消去法和对称扩张,得到了边值问题的可解条件和解的表达式.推广了解析函数的相应理论.     

Kinetics of the oxidation of quercetin by 2,2-diphenyl-1-picrylhydrazyl (dpph•)

In methanol/water, dpph(?) bleaching (519 nm) by quercetin, QH(2), exhibits biphasic kinetics. The dpph(?) reacts completely with the quercetin anion within 100 ms. Subsequent slower bleaching involves solvent and QH(2) addition to quinoid products. The fast reaction is first-order in dpph(?) but only ca. 0.38 order in [QH(2)]. This extraordinary nonintegral order is attributed to reversible formation of π-stacked {QH(-)/dpph(?)} complexes in which electron transfer to products, {QH(?)/dpph(-)}, is slow (k(ET) ≈ 10(5) s(-1)).     

汞扩散泵——镉捕集阱高真空系统

我们在二级玻璃汞扩散泵的真空系统上使用了室温的镉膜阱,证明镉膜阱能有效地捕集汞蒸气,使被抽容器达到气压力10^-5—10^-7毫米汞数量级的高真空。我们较系统地试验了镉膜的条件对于极限气压的影响,实验结果表明,新蒸发的镉膜效果最好;将镉膜在10^-2毫米汞的气压下搁置10小时后对于极限气压的影响不大;但若将其在大气下搁置10小时,则极限气压约升高一个数量级;进一步延长在大气中的暴露时间(达300天),对极限气压无更大的影响。初步的寿命试验表明,扩散泵工作140小时之后,极限气压才较显著地上升。降低镉膜阱的温度、增加镉膜阱的数目和被抽容器的高温烘烤都是提高真空度的有效途径;在实验中考虑了这些因素,我们曾获得了气压低达10^-9毫米汞数量级的超高真空。     

Cross measurements of linear momentum transfer and energy dissipation in collisions between 290 MeV20Ne and238U

The²⁰Ne + U reactions are investigated at 290 MeV bombarding energy. The linear momentum transfer and excitation energy are deduced eventwise from the respective measurements of the folding angle between correlated fission fragments and the neutron multiplicity. A simple incomplete fusion picture is shown to essentially account for the data. The sensitivity of the two measurements in order to infer the violence of a collision is discussed in details.     

Interaction of 80 MeV12C with88Sr; Neutron transfer,inelastic scattering and spin alignment of the 2+ State of12C

Level structure of¹⁰²Cd has been studied via both¹⁰²In decay and nuclear reactions. Using⁹²Mo+¹⁴N at 86 MeV, the nucleus¹⁰²In was identified and its decay (T _1/2=24 ±4s) studied with the aid of on-line mass separation techniques. Levels of¹⁰²Cd were also populated with⁹²Mo+¹²C at 50 MeV and¹⁰²Pd+³He at 35 MeV reactions and investigated by means of standard in-beam techniques. A level scheme including states up to 4.5 MeV excitation energy is proposed and then discussed in the frame of available calculations.     

电荷转移配合物(C7H10NO)3[PW12O40]·6H2O的合成、性质及晶体结构

以十二钨磷酸和对甲氨基苯酚硫酸盐为原料合成了组成为(C7H10NO)3[PW12O40].6H2O的新型电荷转移配合物,通过元素分析、红外光谱、溶液紫外-可见光谱、固体漫反射光谱、X光电子能谱、循环伏安、热重-差热分析和X射线单晶衍射对其进行了表征.配合物晶体属单斜晶系,P2(1)/c空间群,晶胞参数:a=1.504 84(16)nm,b=2.966 8(3)nm,c=1.504 84(16)nm,β=117.82°,V=5.941 8(11)nm3,Dc=3.753 g/cm3,Z=4.结构分析表明,化合物分子由1个杂多阴离子,3个C7H10NO 阳离子和6个结晶水分子组成.电子光谱显示,在N,N-二甲基甲酰胺(DMF)溶剂中或固态情况下有机底物和杂多阴离子间存在电荷转移作用.热分析表明配合物的热分解分3步进行,其杂多阴离子分解温度为588.4℃.