苯乙烯

Chiral ligands mentioned above and their complexes with acetate copper were used as enantio-selective catalysts in asymmetric cyclopropanation reactions of diazoacetate and 1,1-diphenyl ethylene. Investigations indicate that all of them reveal certain optical-selective capability, but chiral C2-symmetric 2,6-bispyridine ligands show better catalytic capability than chiral asymmetric schifF-base ligands.

选择了2个手性2，6-吡啶双噁唑啉配体和6个手性不对称席夫碱配体与醋酸铜形成的配合物作为催化剂，对重氮乙酸乙酯与1，1-二苯乙烯不对称环加成进行催化反应，发现这8个催化剂对1，1-二苯乙烯的不对称环丙烷化反应都表现出了一定的光学活性诱导能力，手性2，6-吡啶双噁唑啉-铜类具有比手性Schiff碱-铜类更好的催化性能。

Oligomeric poly (sodium styrenesulfnate-co-styrene), denotated P, was synthesized by means of radical polymerization, layered.

采用自由基溶液聚合的方法将苯乙烯与对苯乙烯磺酸钠共聚，合成了低聚物P。

In the asymmetric epoxidation of cis-β-methylstyrene, the selectivity and enantiometric excess for the epoxides reached 96% and 78%, respectively. The recyclability of the catalyst was also studied.

结果表明，该配合物对顺－β-甲基苯乙烯的不对称环氧化反应具有很好的催化性能，产物选择性达96%，ee值达78%，以顺－β-甲基苯乙烯为底物，m-CPBA为氧化剂，考察了该配合物催化剂的循环使用性能。

A series of new isoxazolines were prepared by 1,3-dipolar cycloaddition between different mono-substituted styrenes and new 1,3-dipolar compounds which were synthesized by the reaction of N-methylhydroxylamine sulfate with aromatic carbonyl compounds.

以N-甲羟胺硫酸盐和芳香族羰基化合物为主要原料合成了一系列不同的1，3-偶极化合物，并合成了四种不同的单取代苯乙烯。以该系列1，3-偶极化合物和单取代苯乙烯为主要中间体，采用1，3-偶极环加成反应合成了一系列异恶唑啉类新化合物。

The effect of the amount of solvent was not distinct. In the molybdenum blue- di-n-octyltin oxide system, besides the effect of the amount of catalyst, oxidant, phase transfer, solvent and the reaction time, the effect of reaction temperature on the synthetic reaction of styrene oxide was researched.

在钼蓝-氧化三丁锡体催化系中，除研究了溶剂用量、催化剂用量、氧化剂用量、相转移剂用量以及反应时间对氧化苯乙烯收率的影响外，还研究了反应温度对催化氧化苯乙烯反应的影响。

In the mixed solvent of dimethyl phthalate / TBP or phenyl ether / TBP, the selectivity for styrene oxide is good but the conversion of styrene is low due to the coordination to the catalyst of the solvent.

邻苯二甲酸二甲酯或二苯醚等与磷酸三丁酯的混合溶剂中环氧化的选择性较高，但由于溶剂对催化剂的配位作用抑制了催化剂的活性，苯乙烯转化率很低；当部分的邻苯二甲酸二甲酯或二苯醚被甲苯取代后，苯乙烯的转化率提高，生成环氧苯乙烷的选择性不变。

In this thesis, this system is used for epoxidation of propylene and styrenewith good results. The solvent effect is investigated for epoxidation of styrene. In the mixedsolvent of dimethyl phthalate / TBP or phenyl ether / TBP, the selectivity for styreneoxide is good but the conversion of styrene is low due to the coordination to thecatalyst of the solvent. When part of dimethyl phthalate or phenyl ether is replacedby toluene, the conversion increases and the selectivity keeps constant.

邻苯二甲酸二甲酯或二苯醚等与磷酸三丁酯的混合溶剂中环氧化的选择性较高，但由于溶剂对催化剂的配位作用抑制了催化剂的活性，苯乙烯转化率很低；当部分的邻苯二甲酸二甲酯或二苯醚被甲苯取代后，苯乙烯的转化率提高，生成环氧苯乙烷的选择性不变。

In the dissertation, a new stabilization method, equal-density method was adopted to prepare modified asphalts with storage stability at high temperature. In this method, a compound was prepared by premixing polymer and filler, and the compound was mixed with asphalt to prepare Polymer-Modified Asphalt by changing the ratio of polymer and filler. The asphalts with good storage stability were formed with the addition of filler, by regulating the density difference between polymer and asphalt. With identifying the effect of composition factor and the technique conditions on mechanical properties of polymer/filler compound and the molecular distribution of the polymer, identifying the effect of composition factor and the technique conditions on the properties and structure of polymer/filler modified asphalt, Styrene-Butadiene-Styrene copolymer, Low Density PolyEthylene, Styrene-Ethylene-Butadiene-Styrene block copolymer modified asphalts with good storage stability and performance were prepared. Rheological method, gel content analysis and swelling measurement were adopted to elucidate the interaction between the polymer and filler. Filler reduced the difference between the polymer and asphalt with the premixing technique, which led to the improvement of the storage stability of the modified asphalts. The thermo-oxidative aging process of base asphalt and PMA were studied and the effect of antioxidant additives on the base asphalt and PMA were analyzed.

本论文采用等密度方法，即预先混合聚合物与填料制备复合物，复合物在沥青中会吸收油份而溶胀，改变填料的用量从而调节聚合物与沥青的密度差异的方法，制备出高温贮存稳定的改性沥青，并研究了工艺条件和配方因素对聚合物/填料复合物力学和聚合物分子量分布的影响，系统考察了工艺条件和配方因素对聚合物/填料改性沥青性能与形态结构的影响，研制出性能优良、高温贮存稳定的苯乙烯-丁二烯-苯乙烯三嵌段共聚物、氢化SBS、低密度聚乙烯改性沥青，并通过流变学分析方法及凝胶和溶胀测试探讨了聚合物与填料的相互作用，指出经过预混工艺填料改变了聚合物与沥青的密度差异，以此说明聚合物/填料改性沥青高温贮存稳定的原因；研究了基质沥青和聚合物改性沥青热氧老化过程，并分析了抗氧剂对基质沥青及聚合物改性沥青的影响，探讨了抗氧剂提高沥青耐老化性能的原因。

The chemical kinetic modeling of NO reduction by a typical tar model compound is studied, in order to discover the mechanism of NO reduction by tar. Base on the mechanism of NO reduction by hydrocarbon and non-hydrocarbon intermediates produced in the tar oxidative decomposition, the chemical kinetic modeling of NO reduction by toluene is studied.

分析结果表明，苯、甲苯、苯乙烯和苯酚均有明显的累积离子流峰面积，是生物质焦油的主要组分，涵盖了初级、二级和三级焦油产物，所以选取苯、甲苯、苯乙烯和苯酚作为典型的生物质焦油的模型化合物。

Based on the-references on the thermal imidization of polyand the polymer composition analysis,the thermal imidization mechanism of SMA with aniline was demonstrated to be a two-stage consecutive reaction,in which a second-order reversible ring-opening reaction of SMA to produce poly(styrene-co-N-phenyl-maleamic acid)and a first-order irreversible intrachain ring-closing reaction to form SNPMI were involved.

论文首先参考聚酰胺酸热环化反应，并通过SMA酰亚胺化产物的组成分析，确定了SMA与苯胺的热酰亚胺化反应机理为一个包含由SMA生成苯乙烯—N-苯基马来酰胺酸共聚物的二级可逆开环反应以及由SNPMA生成苯乙烯—N-苯基马来酰亚胺共聚物的一级不可逆分子内闭环反应在内的串联反应过程，其中第二步SNPMA闭环反应为控制步骤。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。