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imine相关的网络例句

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与 imine 相关的网络例句 [注:此内容来源于网络,仅供参考]

The three steps, imine-formation, reduction and intramolecular amidation, were completed in one-pot at room temperature.

Schiff碱的制备、还原、酯的胺解三步在"一锅"内完成。

Because of the participation of C(3)-OH, treating imine 40 using classic Nef reaction condition did not give the expected product with ketone group at C-17 rather than a novel compound 43 isolated as blue amorphous powder.

采用经典的Nef反应条件未能得到预期的17-酮,而是生成了C(3)-OH参与反应的产物43。

The integrated analytical results show that the novel ligand coexists in ketoform and enolform structures under the measuring conditions, the ketoform structure may change into the enolform structure during the coordination and bonds with the central ion by two O atoms of the enolized hydroxyl group of pyrazolone ring and H2O and the N atom of the imine group and the N atom containing H of benzimidazole ring by losing the proton. And the coordination number of these complexes is four.

综合各种分析结果显示:配体在测试条件下以酮式和烯醇式结构共存,配位时酮式可能转化为烯醇式结构,按去质子的方式以吡唑啉酮环羟基和H2O上的两个O原子以及亚胺基上的N原子和苯并咪唑环上的含氢N原子与中心离子成键,配合物的配位数为4。

In this review, basically classified by the chemical construction of dendritic skeleton, mainly focusing on the polyamidoamine, polypropylene imine, polycarbosilane, polyether and polyester systems, the recent advances in the rationally designed syntheses and their self-organized superstructure of side-chain LC dendrimers have been summarized and commented.

本文按树枝状大分子骨架的化学结构分类,对侧链型树枝状大分子液晶的设计合成、液晶相行为及其自组织超结构的最新研究进展进行总结和评述,重点介绍了聚酰胺-胺、聚丙烯亚胺、聚碳硅烷、聚醚以及聚酯树枝状大分子液晶体系。

However, poly analogs cannot be obtained through the polymerization of the obvious parent molecule, vinyl amine, because vinyl amine is unstable with respect to its imine tautomer, ethylimine.

然而,聚类似物不能获得通过聚合明显的母公司分子,乙烯胺,因为乙烯胺是不稳定与尊重其亚胺互变异构体, ethylimine 。

The three steps, imine-formation, reduction and intramolecular amidation, were completed in one-pot at room temperature.

Schiff碱的制备、还原、酯的胺解三步在&一锅&内完成。

In order to develop an useful synthestic process, we have synthesized amides with various substitutents. The isoquinoline skeleton was constructed through Bischler-Napieralski reaction, followed by asymmetric reduction of the imine intermediates with a Ru complex to form the only chiral center. Finally, we connected the two phenyl groups by Heck reaction and effectively obtained optically active aporphine alkaloids.

为了发展一套实用的合成方法,我们首先制备於苯环上具有不同种取代基的苯乙醯胺,接著透过Bischler-Napieralski反应进行分子内合环,并利用钌金属对亚胺中间体进行不对称的还原反应,建立出产物中唯一的光学活性中心,最后再利用Heck反应连结两个苯环,就可以顺利得到具有光学选择性的阿朴吩类天然物。

Schiff base is the Types of organic compounds which contain C-N double bond of the imine or azomethine group characteristics.the early research focus on Amine Schiff base reduction.

席夫碱主要是指含有碳氮双键的亚胺或甲亚胺特性基团的一类有机化合物,早期的研究一般为缩胺类席夫碱。

The second part is about that five-membered rings compounds were synthesised using aromatic aldehyde,α-bromoketone and imine ester in the present of zinc power.

2以芳香醛,α-溴代苯乙酮与氨基酸酯亚胺类化合物在金属锌粉的作用下,生成一系列的四氢吡咯化合物。

Dealcoholization temperature markedly influences the surface area and porosity of the resultant MAO-supports. When the support was pretreated at lower or higher temperature, the corresponding MAO-support shows very low surface area;2.XRD and IR analyses indicate that MAO has reacted with the residual ethanol in the supports, which is an important manner to get MAO fixed on the carrier. Morever, XPS analyse indicates that MAO can also be coordinated with MgCl_2, which is another way to get MAO fixed on the support;3.ICP and EDX analyses indicate that dealcoholization temperature not only determined the element content on the solid catalyst, but also influences the element distribution on the carrier;4.The activities of the supported phenoxy-imine catalysts and the properties of resultant polymers are strongly dependent on the dealcoholization temperature. The support (MSP-5) obtained by treating MgCl_2·2.56C_2H_5OH at 160℃for 4 h, then modified by MAO is very effective for immobilizing complex 3, the resultant solid catalyst (MSPC-5) shows very high activity in ethylene polymerization, and its kinetics of polymerization is stable during the reaction process. Finally, PEs with spherical morphology and high bulk density (over 0.35g/ml) were obtained, without reactor fouling;5.In this work, polymerization conditions such as alkylaluminums, Al/Zr ratio, temperature and H_2 had a pronounced effect on the activity of MSPC-5 and properties of PE;(3). New MgCl_2-Supported Single-Site Catalysts for Ethylene PolymerizationIn this work, a kind of new MgCl_2 support was obtained by anhydrous MgCl_2 co-milled with solid MAO, and it is a creative contribution. Then some single-site catalysts were supported on the new MgCl_2 support, and the resulted solid catalysts were tested in ethylene polymerization, the results indicated that:1.XRD and IR analyses indicate that MAO does be coordinated with MgCl_2, which is in good agreement with the results obtained by XPS;2.co-mlling time had no obvious effect on the texture of support after 12 hours;3.In this work, MgCl_2 was co-milled with solid MAO for different hours, and then complex 3 was supported on these co-milled supports. It was found that co-milling time markedly influences the activity of solid catalysts, but it had negligible effect on the kinetic profile and the properties of resultant PE.

XPS研究结果表明,MAO不仅仅只和乙醇作用,MAO还与MgCl_2本身有一定的作用,这是一个极为重要的发现;3、通过ICP和EDX表征,发现载体的脱醇温度直接影响着元素在固体催化剂中的含量及分布;4、脱醇温度极大地影响着负载苯氧基亚胺类催化剂的活性和聚合物的性能,特别是原始载体经160℃活化4小时制备得到的固体催化剂MSPC-5的活性明显高于其他脱醇温度条件下制得的固体催化,并且催化剂寿命长,表现出稳定的动力学行为,最终获得了高堆密度(大于0.35g/ml)的球形聚乙烯颗粒;5、本文选择MSPC-5为研究对象,考察了聚合反应参数对催化剂的活性及其聚合物的影响,研究发现:不同的烷基铝对催化剂具有非常重要的影响,特别足TIBA对MSPC-5的助催化活性最高,烷基铝的加入量有一个较佳值,聚合温度为80度时活性最高,H_2的加入使催化剂的活性明显降低且聚合物的分子量也减小;、新型氯化镁载体负载单活性中心催化剂催化乙烯聚合本文创造性采用固体MAO与无水氯化镁直接进行共研磨,制备出了一种的新型的氯化镁载体,并将该载体用于多种单活性中心催化剂的负载化研究,研究表明:1、通过BET、XRD的表征,再次证实了MAO与MgCl_2之间具有直接作用,与XPS的研究结果相一致;2、当研磨时间高于12小时时,延长研磨时间对载体的结构没有显著的影响;3、将配合物3负载于共研磨时间不同的一系列载体上,乙烯聚合结果表明,尽管共研磨时间对负载催化剂的活性具有明显的影响,但是它对聚合物的性能以及催化剂的影响不明显。

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