新显色剂对溴苯酚偶氮若丹宁光度法测定Au（Ⅲ）的研究

提出了以显色剂对溴苯酚偶氮若丹宁[5-(5-溴-2-羟基苯偶氮)若丹宁]作为光度法测定Au(Ⅲ)试剂的新方法。在1.2mol·L~(-1)盐酸介质及阴离子表面活性剂十二烷基苯磺酸钠(SDBS)存在下,Au(Ⅲ)与试剂形成桔红色配合物,545nm处有最大吸收,摩尔吸光系数ε为7.75×10~4,Au(Ⅲ)浓度在0～44μg/25ml范围内服从比耳定律。方法灵敏度高,选择性好,配合物的稳定时间长,操作简便,已成功地应用于含金废水中Au(Ⅲ)的测定。     

高阻隔材料——偏氯乙烯悬浮共聚树脂

本文介绍偏氯乙烯悬浮共聚树脂的优异阻隔性能、合成配方与工艺。     

Band structure studies on crystalline C60, Ca3C60, and Ca5C60

The three-dimensional EHMO crystal orbital calculations for crystalline C₆₀, Ca₃C₆₀, and Ca₅C₆₀ are reported. The ground states of both undoped solid C₆₀ and partially doped Ca₃C₆₀ are found to be insulating with an indirect energy gap of 1.2 and 0.5 eV, respectively. In contrast, Ca₅C₆₀ forms a metallic conducting phase with a set of three half-filled bands crossing the Fermi level, which is found to be located close to a peak of the density of state. The character of crystal orbitals near the Fermi level for both Ca₃C₆₀ and Ca₅C₆₀ is completely carbonlike. In both cases, the Ca atoms are almost fully ionized and C₆₀ molecules form a stable negative charge state with six to 10 additional electrons. © 1995 John Wiley & Sons, Inc.     

同步辐射白光全反射XRF在痕量元素检测的初步应用研究

叙述了同步辐射白光全反射Ｘ射线荧光分析的实验装置，给出了几种标准物质ＴＸＲＦ实验的检出限，并对实验结果进行了讨论。     

6(5H)-phenanthridinones. II. Preparation of substituted 6(5h)-phenanthridinones from 9-oxofluorenes

A number of 6(5H)-phenanthridinones have been conveniently prepared from 9-oxofluorenes through the Schmidt reaction. It has been found that all amino and nitro 9-oxofluorenes thus far tried gave substituted 6(5H)-phenanthridinones with the amino or nitro group situated in the benzene ring attached to the nitrogen of the lactam group. UV and IR spectral data are presented for these compounds.     

Study on the supramolecular system of TAPP with cyclodextrins by polarography

The interaction of cyclodextrins with meso- Tetrakis (4-N-trimethylaminobenzyl) porphyrin (TAPP) in 0.1 mol l(-1) phosphate buffer (pH 7.0, 20 degrees C) has been studied by polarography. The TAPP can form the 1:1 inclusion complex with Sulfobutylether-beta-cyclodextrin (SBE-beta-CD) and1:2 inclusion complexes with other four cyclodextrins. A new expression, which is used to calculate the inclusion constant for1:2 inclusion complex by polarography, has been educed and testified firstly in this paper. Furthermore, the inclusion abilities of different kinds of cyclodextrins are compared. The result shows the inclusion ability of anionic cyclodextrin SBE-beta-CD with cationic porphyrin TAPP is very strong. It suggests that the charge attraction between CDs and TAPP plays an important role in the inclusion procedure except for the hydrophobic effect. The inclusion formation of anionic cyclodextrins with drugs can increase released rate of drugs at high pH; therefore, the suparmolecular data for the controlled release of the drugs that owned the similar properties as hematoporphyrin have been offered by polarography in this paper.     

Studies on the determination of diacetyl guanfubase A concentration in rabbit plasma and pharmacokinetics

A gas chromatographic method for monitoring diacetyl guanfubase A in plasma is described. The procedure involved a single solvent extraction of drug from rabbit plasma into ethyl acetate with guanfubase A as an internal standard. The extract was analyzed subsequently on a gas chromatograph equipped with a hydrogen flame ionization detector. The recovery was 86.43% +/- 6.90% (+/- SD); the RSD of within-day and between-day was 2.81%-5.26% and 5.22%-8.24%, respectively; the regression line was linear over the concentration range of 25-200 micrograms/mL, the limit of detection was 10 micrograms/mL. No endogeneous interference was found in chromatograms of the biological samples. This method was applied to the pharmacokinetic study of diacetyl guanfubase A in rabbits.     

面向化妆品产业升级的江南大学应用化学专业建设思考与实践

Based on the development prospect of cosmetics industry, the advantage of light industry characteristic and the foundation of applied chemistry in Jiangnan University, a systematic upgrading of applied chemistry was carried out through "emerging engineering education (3E)" project "upgrade and practice of chemistry-related majors of local and/or trade university responding to the social developments" supported by the Ministry of Education. On the basis of investigation and analysis, the orientation and training goal of applied chemistry were updated first, and then the curriculum system was determined and the curriculum construction is strengthened, so as to achieve more distinctive characteristics, more solid foundation and more comprehensive quality. In view of the new requirements of the 3E for talent training, some practices have been formed in the aspects of multi-disciplinary integration, multi-angle coordination and close integration to industry. Contributing the development of cosmetics industry and seizing the commanding point of science and technology from the perspective of talent training, will play a unique role in human social progress.     

Controllable and flexible cellular network for virus cell-to-cell spread

Cellular networks were constructed based on PEG modification and soft lithography, in which cell numbers and spatial distributions can be controlled. A micro-injector was combined with cellular networks to fix virus induced plaque and virus spread direction, by which virus cell-to-cell spread can be distinguished from cell-free spread.     

SYNTHESIS OF BLOCK COPOLYMER FROM 5,6 -BENZO-2-METHYLENE-1,3-DIOXEPANE AND METHYL ACRYLATE VIA ATOM TRANSFER RADICAL POLYMERIZATION

Poly(methyl acrylate)-b-poly(5,6-benzo-2-methylene-1, 3-dioxepane) (PMA-b-PBMDO) was synthesized by two-step atom transfer radical polymerization (ATRP). Firstly, ATRP of methyl acrylate (MA) was realized using ethyl α-bromobutyrate (EBrB) as initiator in the presence of CuBr/2,2'-bipyridine. After isolation, poly(methyl acrylate) withterminal bromine (PMA-Br) was synthesized. Secondly, the resulting PMA-Br was used as a macromolecular initiator in theATRP of BMDO. The Structure of block copolymer was characterized by ~1H-NMR spectroscopy. Molecular weight andmolecular weight distribution were determined on a gel permeation chromatograph (GPC).