偶二氮化合物

基本解释 (translations)

tetrazone

与偶二氮化合物相关的网络例句 [注：此内容来源于网络，仅供参考]

Based on the mechanism of coupling reaction,the reaction of melt metallocene-based Poly(Ethylene-α-Octene) initiated by dicumyl peroxide was studied at elevated temperature in oscillatory shear flow field.

以苯胺、环氧丙烷为原料制备了N，N 二(2 羟丙基)苯胺，然后NHPPA与对硝基苯胺通过重氮偶合反应制备了一种具有推拉电子结构的偶氮化合物4 硝基 4′ N，N 二(2 羟丙基)氨基偶氮苯。

The application properties of azo pigements as charge-generating material, in organic photoconductors is discussed. Some types such as xanthone, bisbenzofluorenone, benzoxazole are specially reviewed. Their application properties are compared with other charge-generating materials.

论述了偶氮类电荷产生材料在有机光导体中的应用，重点讨论了氧杂蒽酮类、苯并哑唑类、二苯并芴酮类等偶氮化合物作为电荷产生材料的光电性能，并且将它们与以前使用的电荷产生材料相比较。

In chapter four, the preperation of ytterbium diiodide was examined. The reductive cleavage of Se-Se bond and S-S bond induced by ytterbium diiodide was investigated. The reaction of diselenides and disulfides with allylic bromide promoted by ytterbium diiodide was also examined. The intermolecular Barbier-type reaction induced by ytterbium diiodide was studied. In the last section of this chapter, the intermolecular reductive coupling of nitriles with azides induced by samarium diiodide was investigated.

第四章，研究了二碘化镱的制备方法，以及二碘化镱作为一种优良的单电子转移试剂在有机合成中的应用：二硒醚的Se--Se键和二硫醚S-S键的还原断裂，及其在合成烯丙基硒醚，硒代酯和烯丙基硫醚，硫代酯中的应用，实验结果表明二碘化镱也能促进分子间的Barbier反应，而文献认为二碘化镱不能促进分子间的Barbier反应；最后研究了二碘化钐促进的叠氮化合物与腈的交叉还原偶联反应，一步高收率地制备脒的方法。

Even carbon number alkenes, phthalic esters and nitrogen heteroatom-containing components were detected in the elution fractions, while such components were not detected without silica gel column separation, indicating that preseparation is very important for increasing the sensitivity of GC/MS analysis.

各洗脱馏分用GC/MS分析，其可测成分与直接检测相比，多检测出偶碳烯烃、邻苯二甲酸酯类和含氮化合物等，表明合适的预分离对提高GC/MS分析的灵敏度非常重要。

The reaction can be carried out in a non-aqueous solution and 4-aminopyridine can be diazotized with this method.

这个方法表现出如下优点：1），整个重氮化与偶联反应均在非水溶剂中进行；2），改变原料不同投料比，可以分别得到含有一，二，四偶联产物为主的反应产物；3），可以合成在酸性水溶液中不易重氮化的4-氨基吡啶的偶氮化合物。

In the first part of this thesis, a formal [4+2] cycloaddition of ketenes with N-benzoyldiazenes catalyzed by chiral NHCs was studied, which gave 1,3,4-oxadiazin-6-ones in very high yields and enantioselectivites.

论文的第一部分内容是在手性氮杂环卡宾的催化下，烯酮与N-苯甲酰偶氮化合物的环加成反应，合成各种手性的噁二嗪酮，它们还可以经过简单的两步一锅法制备手性氨基酯。

The structures were identified by IR, UV,〓 NMR and element analyses. 2. Free radical 4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxyl as catalyst, the phase transfer catalyzed method of oxidation eighteen semicarbazides to N-Aryl-2-Phenyl diazenecarboxamide with a solution of potassium ferricyanide in 2N aqueous sodium hydroxide and dichloromethane is described for the first time.

利用2，2，6，6-四甲基-4-羟基-1-哌啶氮氧自由基为相转移催化剂，在饱和铁氰化钾的2N氢氧化钠溶液与二氯甲烷的两相反应液中，催化氧化十八个取代氨基脲得到十八个相应的新型偶氮化合物N，2-二芳基二氮亚烯甲酰胺，均获得了较高的产率。