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Recent progress in the applications of non-enzymatic system about Lewis acid and base tokinetic resolution reactions of racemes is reviewed.

本文讨论了路易斯酸及路易斯碱催化体系在外消旋体动力学拆分反应中应用的最新进展。

The cat-alytic systems of Lewis acid and base are useful ways in the non-enzymatic catalysis. They were widely used to different kinds of kinetic resolution reactions. At present, mighty advances have been made in the field.

在非酶催化反应中，路易斯酸碱催化是比较常用的方法，它们被广泛地用于多种外消旋体的动力学拆分反应中，目前在该领域取得了很大的进展。

The catalytic systems of Lewis acid and base are useful ways in the non-enzymatic catalysis. They were widely used to different kinds of kinetic resolution reactions.

在非酶催化反应中，路易斯酸碱催化是比较常用的方法，它们被广泛地用于多种外消旋体的动力学拆分反应中，目前在该领域取得了很大的进展。

In this reaction, DMSO may act as a Lewis base to activate the nucleophile, which facilitates the ring-opening reactions.

与此同时，我们还发现在DMSO中，无催化剂的中型条件下，硫，胺以及各类硅亲核试剂可以对氮杂环丙烷化合物开环。

Density functional theory calculations at the B3LYP/6-31G level of theory were employed to study the mechanism and the potential energy surface of Diels-Alder reactions between Lewis base stabilized borabenzene and dienophiles.

采用密度泛函理论方法在B3LYP/6-31G水平上研究了Lewis碱稳定的硼代苯与一些亲二烯体的两种可能的Diels-Alder反应的微观机理和势能剖面，并研究了反应的溶剂效应和取代基效应。

During this period significant analytical contributions to chemistry include the development of systematic elemental analysis by Justus von Liebig and systematized organic analysis based on the specific reactions of functional groups.

这一时期分析化学对化学的贡献为：尤斯图斯-冯-李比希的系统元素分析、以官能团特殊反应为依据的系统化有机分析。

According to our present broadcasting situation,the thesis proposes using new technology to update and reform the present HFC. It also suggests broadcasting using self-advantage and arranging EPON in order to win the supermarket.

论文从我国广电的现状出发，结合实际，积极倡导采用新技术更新、改造我国现有的HFC网络；倡导广电现阶段利用自身优势，部署EPON网络来赢取市场。

A new general kinetic equation was derived in which the effect of the removal of condensation water was taken into account completely, and was applied to the polyesterification kinetic study of AA/HPHP and AA/NPG. It was found that the reaction order of self-catalyzed polyesterification was not constant. For these polyesterifications, the reaction order was 2.5 at a low temperature, while 3.0 at a high temperature.

考虑缩合水的排除对反应体系的影响，用体积浓度单位推导出一个新的聚酯反应总包动力学方程，并应用到AA/HPHP和AA/NPG两个聚酯化反应的动力学研究中，研究发现，自催化聚酯反应的反应级数并不是固定值，对于AA/HPHP和AA/NPG两个聚酯化反应而言，低温时反应级数为2.5，高温时反应级数为3.0。