蒙药心舒安中锗的差分脉冲极谱研究

在pH=1.30的H2SO4和3,4-二羟基苯甲醛(DHB)底液中,采用差分脉冲极谱法,测得无机锗的脉冲极谱波.其峰电位为Ep=-0.53V.Ge(Ⅳ)浓度在1.03×10-3-1.04×10-4mol·L-1范围内与峰电流呈线性关系,样品中总锗和无机锗的回收率分别是95.72%和96.43%.     

The highly chemoselective transfer hydrogenation of the carbon–carbon double bond of conjugated nitroalkenes by a rhodium complex

Chemoselective transfer hydrogenation of conjugated nitroalkenes catalyzed by [RhCl₂Cp¹]₂–diamine complex (Cp¹=η⁵-C₅Me₅) using HCOOH/Et₃N (5:2) (TEAF) as a hydrogen source was realized. A variety of nitrostyrenes, β-methyl nitrostyrenes, and 3-methyl-4-nitro-5-alkenyl-isoxazoles were reduced smoothly in good to excellent yields in short reaction time. Other functional groups are inert under the reaction conditions.     

Loschmidt echo of a central spin coupled to an XY spin chain: Role of three-site interaction

Effects of two types of three-site interaction, i.e., XZX+YZY and XZY−YZX, on Loschmidt Echo (LE) of a central spin coupled to an XY spin chain are studied. The dynamical evolution behaviors of the LE are investigated analytically and numerically. The XZX+YZY type of three-site interaction (α₁) can shift the critical points of the magnetic field λ. At the critical points |λ−α₁|=1, the decay of the LE is enhanced. The role of the XZY−YZX type of three-site interaction (α₂) depends on its strength. In some specific intervals, α₂ can remarkably delay the decay of the LE.     

Novel Covalently Linked Self-Assembled Films from a Functional Hyperbranched Conjugated Poly(Phenylene Vinylene)

The hotSPOt in the fields of molecular films focuses on highly ordered, ultrathin filmswith molecularly controllable surface properties. It is attractive tO stUdy supramolecularfunctional POlymeric materials with suitable physical properties and abilities to formorganized superstrUctures at the interfacesl'2'3A. Dendritic macromolecules are a kind ofmaterials which is capable of self-organizing into superstrUctUres'. So a new dendrimerlike POly(Phenylene vinylene)- --hyperbranched conj "…     

Extraction-spectrophotometric analysis of palladium in the reprocessing waste of spent nuclear fuels using benzo-15-crown-5 and iodide

Based on the previous studies, a procedure has been established for the analysis of palladium in reprocessing waste solution of spent nuclear fuel. The sample was contacted with the extractant solution which consisted of benzo-15-crown-5, chloroform, and potasium iodide at room temperature for 1 minute. The extract was dehydrated by anhydrous Na₂SO₄ and measured spectrophotometrically versus water at 360 nm. The extractant solution used can be regenerated by KI (or NaI and Lil) for reuse. The percent extraction of palladium and apparent molar abaorptivity are 96–100% and 4·10⁴, respectively. The composition of extracted complex is [KB15C5)₂]₂·(Pd₂I₆).     

透射式GaAs光电阴极的X射线衍射研究

本文介绍了高精度多晶多反射X射线衍射仪的一种新的应用.首次将其应用于研究高灵敏度第三代微光象增强器中由掺Zn的p型GaAs/GaAlAs、玻璃组成的光电阴极的材料特性；发展了用倒格子空间衍射图方法评价光电阴级组件晶体质量的方法.通过分析得知,衍射强度在倒格子空间沿。方向展宽主要起因于晶体中的嵌镶效应的增强.文中采用衍射动力学理论的计算方法并忽略初始条件,模拟后得到的曲线与衍射强度沿ω/θ方向的投影强度曲线符合的比较好.粘接良好的阴极样品表明,GaAs/GaAlAs晶格常数的变化基本上可以消除,但粘接引起的嵌镶效应的增强却不能完全消除.     

NH4Cl作助熔剂合成CaS：Ce的光谱特性及其浓度效应

以ＮＨ４Ｃｌ作助溶剂，碳还原硫酸钙的方法合成了ＣａＳ：Ｃｅ。在紫外光激发下，ＣａＳ：Ｃｅ中存在着Ｃｅ＾３＋的＾２Ｄ－＾２Ｆ５／２（５００ｎｍ）和＾２Ｄ－＾２Ｆ７／２（５５０ｎｍ）跃迁发射，但在蓝色光激发下，只有波峰为５３２ｎｍ半宽度为９２ｎｍ的宽带发射。当Ｃｅ＾３＋的浓度为０．０７５ｍｏｌ％时，＾２Ｄ－＾２Ｆ５／２跃迁发射强度与＾２Ｄ－＾２Ｆ７／２跃迁发射强度相等，而５３２ｎｍ发射猝灭。     

Studies on the structures and syntheses of arteannuin and related compounds: XV. Determination of A/B ring configuration of arteannuic acid

5-Oxo-compound 7 and its epimer 8 prepared from epoxidation of methyl arteannuinate followed by rearrangement with BF₃ · Et₂O exhibited a negative and a positive Cotton effect near 294 nm in CD, respectively, a cis A/B ring fusion for 7 and a trans A/B ring fusion for 8 were assigned. It is consistent with the prediction from the octant rule. Therefore the cis A/B ring fusion for arteannuic acid is established. In a similar way, compounds 13a, b and 14 were obtained from the dihydroarteannuinate. Compounds 13a, b showed the same signs as that of 7 and compound 14 as that of 8. Thus the cis A/B ring configuration of arteannuic acid is further proved.     

C and Si ion implantation and the origins of yellow luminescence in GaN

We have studied the influence of C and Si ion implantation with different implantation doses on yellow luminescence (YL) from GaN. Three kinds of GaN samples were used. In their as-grown states, #1 samples had strong YL, #2 samples had no YL, while #3 samples had weak YL. Our experimental results show that: (i) after annealing at 950 °C, the YL intensity for Si ion implanted #1 sample decreased with increasing implantation dose, while that for C ion implanted #1 sample exhibited a reverse rule; (ii) for #2 samples, C ion implantation produced much stronger YL than Si ion implantation did after annealing at 950 °C; (iii) the YL intensity sequence for Si ion implanted and 950 °C annealed #1, #2, and #3 samples was consistent with that for the unimplanted #1, #2, and #3 samples. However, the YL intensity sequence for the C ion implanted and 950 °C annealed #1, #2, and #3 samples reversed with that for the unimplanted ones. In order to explain all these phenomena, we suggested a physical model which claims that the deep C center is another important origin of YL in GaN, and during C ion implantation, the C ion prefers to combine with a V_Ga to form a C_Ga. PACS 78.55.-m, 85.40.Ry, 68.55.Ln     

Macrocycle-Derived Functional Xanthenes and Progress Towards Concurrent Detection of Glucose and Fructose

The detection of saccharides in biological media is of great current importance for the monitoring of disease states. We have previously reported that solutions of boronic acid-functionalized macrocycles form acyclic oligomeric materials in situ. The oligomers contain fluorescent xanthene moieties. Current efforts are aimed at modulating the spectroscopic responses of these materials for the analysis of specific sugars. We describe conditions whereby the xanthene boronic acids exhibit high colorimetric fructose selectivity. In contrast, at physiological levels selective glucose monitoring can be achieved via fluorescence. Additionally, we describe a method which exhibits promise for detecting both glucose and fructose at dual wavelengths in the UV-Vis region. Mechanistic rationale for each of these findings is presented.