Effects of Surface Relaxation on Enantiospecific Adsorption on Naturally Chiral Pt Surfaces

Many high Miller index metals surfaces are naturally chiral, offering opportunities for performing enantiospecific chemistry. Previous theoretical treatments of adsorption on these surfaces have used surfaces truncated from bulk crystals. This paper examines the effect of surface relaxation on enantiospecific adsorption on chiral Pt surfaces by using relaxed surface structures determined using density functional theory.     

纤维素衍生化手性固定相的制备和对噻吗洛尔拆分

用超声方法合成了三(3,5-二硝基苯甲酰基)纤维素(CTNB)、三(4-溴苯甲酰基)纤维素(CTBB)、三(苯甲酰基)纤维素(CTB)、三(4-甲基苯甲酰基)纤维素(CTMB)、三(4-硝基苯甲酰基)纤维素(CTPB).将此类衍生化纤维素作为薄层色谱的手性固定相,结合展开剂的优化,对噻吗洛尔对映体进行拆分研究,并对衍生化取代基对拆分效果的影响以及对映体在手性固定相上的拆分机理进行了详细的探讨.     

YAG掺铷——钇铝石榴石激光晶体胶粘剂

YAG掺铷——钇铝石榴石激光晶体胶粘剂以丁腈改性环氧树脂,酚醛变性胺为固化剂,用于掺铷——钇铝石榴石激光晶体与钢套粘接,安装在陕西省人民医院YAG激光医用治疗机,临床应用3年,效果很好。后中国电子科技集团第二十七研究所从1990年开始用YAG激光胶粘剂粘接各类激光产品至今,经高低温试验、振动试验、冲击试验等各项性能测试及15年来工程应用证明,在各类激光产品中从未出现开裂、脱胶现象,性能稳定可靠,其粘接强度、耐冲击、耐振动、耐高低温变化、耐水、耐化学介质、耐光、耐老化性能均好,能满足生产要求,用途广泛,符合激光及各种工程应用。文中详述了酚醛变性胺固化剂的选择及该胶粘剂的性能。     

MCM-41 Heterogenized Chiral Amines as Base Catalysts for Enantioselective Michael Reaction

Cinchonidine and cinchonine have been grafted onto pure silica MCM-41. It has been shown that both supported alkaloids are active catalysts for the Michael addition of ethyl 2-oxocyclopentanecarboxylate and methyl vinyl ketone, anchored cinchonidine being more active and enantioselective than anchored cinchonine. The study of the influence of the polarity of the solvent and reaction temperature on the optical induction shows that there is not a direct correlation between solvent polarity and enantioselectivity, and the maximum optical yield was obtained between 278 and 273 K.     

可双固化树枝形聚酰胺-胺树脂的合成及其涂膜性能研究

探讨了以乙二胺与丙烯酸甲酯交替反应，制备了1．5，2．5代树枝形聚酰胺一胺树脂（PAMAM），对其用甲基丙烯酸缩水甘油酯（GMA）和γ-氨丙基三乙氧基硅烷进行了改性，使其能够紫外光固化和潮气固化。热分析考查了玻璃化温度和热稳定性，并进行了硬度、光泽、光固化速度、潮气固化速度、附着力、柔韧性等测试。     

Influences of zinc oxide and an organic additive on the electrochemical behavior of pure aluminum in an alkaline solution

The corrosion behavior of pure aluminum in inhibited and uninhibited 4 MKOH was investigated by means of hydrogen collection, polarization curve measurement and electrochemical impedance spectroscopy (EIS). The results showed that the corrosion of pure aluminum was greatly inhibited by the addition of ZnO and dimethyl amine epoxy propane (designated as DE). EIS and EDAX analyses revealed that ZnO produces its effect by depositing on the aluminum surface, which increases the overpotential of hydrogen evolution. It was also found that the addition of DE could greatly improve the deposition of zinc layers.     

N，O，O′─三（对甲苯磺酰基）双（2─羟乙基）胺的合成

二乙醇胺和对甲苯磺酰氯在三乙胺存在下，反应生成Ｎ，０，Ｏ′－三（对甲苯磺酰基）双（２－羟乙基）胺，产率９３％。从反应混合物中分离得副产物Ｎ，Ｏ－二（对甲苯磺酰基）双（２－羟乙基）胺。     

Immobilization of new Mn(salen) complex over MCM-41 and its activity in asymmetric epoxidation of styrene

New tetradentate chelates of bis-Schiff bases were synthesized and then these chiral salen ligands were immobilized over mesoporous MCM-41 by using the ion-exchange method. The efficiency of the chiral catalyst was examined in the asymmetric epoxidation of styrene. Chiral Mn(salen) complexes immobilized onto mesoporous MCM-41 were stable during the reaction without any leaching and exhibited relatively high enantioselectivity for epoxidation as compared with homogeneous complexes. This revised version was published online in August 2006 with corrections to the Cover Date.     

二(2-氨基乙基)-(3-氨基丙基)胺的合成新方法

以二(氰基甲基)胺及丙烯腈为原料，通过亲核加成、氢化反应合成了不等臂有机多胺化合物二(2-氨基乙基)-(3-氨基丙基)胺，标题化合物及其中间产物经多种谱学手段表征确证。在优化条件下，产物的总收率为67％，含量99.5％(HPLC)。     

Enantiomer-based specificity in pheromone communication by two sympatricGnathoirichus species (Coleoptera: Scolytidae)

The aggregation pheromone ofGnathotrichus retusus was isolated and identified as (S)-(+)-sulcatol (6-methyl-5-hepten-2-ol). In laboratory and field experiments,G. retusus responded to (S)-(+)-sulcatol, but not to (±)-sulcatol, which was attractive to the sympatric species,G. sulcatus. G. sulcatus did not respond to optically pure (S)-(+)-sulcatol, but began to respond when 1% (R)-(–)-sulcatol was present in an enantiomeric mixture.Research supported by the National Science Foundation, U.S.A. (Grant BMS-74-13643), and the Natural Sciences and Engineering Research Council of Canada (Co-op grant A0243 and Operating Grant A3881 and A3785).