三烯烃

13 K,α-pinene+ p -cymene (429. 05—447. 15 K),β-pinene+ p -cymene (439. 20—448. 66 K) and α-pinene+β-pinene+ p -cymene (432. 17—448. 11 K) were determined at atmospheric pressure (100. 7 kPa) with the modified Ellis still. The thermodynamic consistency of the experimental data was confirmed by means of the Herington method.

采用改进的Ellis平衡釜测定了在常压(100.7 kPa)下三个二元物系α-蒎烯＋β-蒎烯(428.82 K ~ 438.13 K)，α-蒎烯＋对伞花烃(429.05 K ~ 447.15 K)，β-蒎烯＋对伞花烃(439.20 K ~ 448.66 K)和一个三元物系α-蒎烯＋β-蒎烯＋对伞花烃(432.17 K ~ 448.11 K)的汽液相平衡数据，并利用Herington规则，以积分检验法对实验数据进行了热力学一致性检验。

It provides a route tothe compounds which contains three functional groups, two carbon-nitrogentriple bonds and one carbon-carbon double bond. In water, metallic indiumpromotes carbon-sulfur bond coupling reaction of aromatic sulfonyl chloride withsuitable organic halides to afford sulfones. In the last chapter, metallic tin mediated allylation of aldimines with allylbromide was revealed.

第三章，我们研究了在水相介质中金属铟促进的烯丙基溴对1，1-二氰基-2-芳基乙烯的Michael加成反应，生成一个含碳碳双键和二个碳氮叁键的三官能团化合物，另外，金属铟在水介质中还可以促进芳基磺酰氯与卤代烃发生碳硫键的偶联，生成砜。

This paper studied the catalytic transformation performances of hydrocarbon model compounds (such as n-Hexane,cyclohexane,1-Hexene) and sulfur-containing model compounds (such as thiophene,3-methylthiophene and benzothiophene) on ZSM-5 catalysts.

以正己烷、环己烷、1-己烯3种烃类和噻吩、3-甲基噻吩和苯并噻吩三种硫化物为模型化合物，考察了烃及含硫模型化合物在ZSM-5分子筛催化剂上的催化转化性能。

Good thermal stability, High mechanical strength.Used as catalyst or catalyst carrier in the manufacturing of the important industrial products, such as cyanuramide, benzene anhydride, maleic acid anhydride, butadiene rubber, acrylic nitrite, etc.

用途：本产品在三聚氰胺、苯酐、顺丁烯二酸酐、顺丁橡胶、丙烯腈等重要工业品生产中用作催化剂及催化剂载体，也广泛用于石化产品的精制脱除芳烃，也可用于有机气体、液体的选择性吸附分离及离子交换脱除水中多价有害元素等。

The chiralMn complexes, especially Jacobsen\'scatalyst, display high enantioselectivity for asymmetric epoxidation of conjugated cis-di-, tri-and some tetrasubstituted prochiral alkenes in the NaClO biphasic system, but the epoxidationreaction generally requires a long reaction time even in the presence of an axial ligand.

在NaClO两相体系中，手性Mn配合物，尤其是Jacobsen催化剂，对共轭顺式二取代、三取代和部分四取代烯烃的不对称环氧化具有高的对映选择性，然而即使存在轴向配体，环氧化反应也通常需要长的反应时间。

In the course of our study the chemistry of arenes contaning allylic acetates moiety under the catalysis of palladium, we found an efficient synthesis of benzocycles via intramolecular Friedel-Crafts reaction of halogen free 6-acetoxy-4alkenyl arens.

我们在设计钯催化的碳—氢键活化时，发现了含有烯丙基醋酸酯侧链的芳烃的三氟醋酸促进的分子内的Friedel-Crafts反应，从而为有效合成苯并六元环结构提供了一个方便的方法。

The triple bond does not usually react so vigorously at a carbon-carbon double bond .

三键在反应时一般不象烯烃中的碳-碳双键那样剧烈。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。