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双烯合成

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The reaction of polyfluoroalkyl iodides with 4-pentenoic acids initiated by sodium dithionite was realized to give polyfluoroalkyl substituted lactones.

我们研究了多氟烷基碘代烷与4-戊烯酸类化合物等在连二亚硫酸钠引发下的反应,得到了氟烷基取代的内酯化合物,我们将该反应称为氟烷基化内酯化反应;并建立了一个利用该反应合成含氟内酯的新方法,首次利用氟烷基化内酯化反应进行高立体选择性双环含氟内酯及手性含氟内酯等的合成,已合成含氟内酯新化合物50余种。

A novel butterfly-shaped fullerene-diporphyrin triad was designed and synthesized,in which 〓 is in the mid of two porphyrin rings and this structure feature enables it to be apotential candidate for the manufacture of Gr〓tzel solar cell and unimolecular logicalcircuit.

设计并合成了一个新的蝴蝶形富勒烯-双卟啉三元分子并确定了结构,两个卟啉环将〓夹在中间,这样的结构有利于探索增加电子/能量给体数目对电荷/能量向富勒烯传递速率的影响,并且这个分子可望被用于太阳能电池制造和单分子逻辑电路的设计上。

These observations suggest that PVA-MEC is an excellent fluorescent macromolecular material with a convenient method of preparation and had a good water-soluble ability.(2) An acrylic monomer bearing xanthene group, acryloyl-fluorescein was synthesized from fluorescein and acryloyl chloride. The photophysical behaviors of Ac-Flu and its copolymer were explored by recording the fluorescence spectra in solution, solid state and film in detail.

2我们采用基于荧光功能单体制备荧光聚合物的方法,选择荧光素为发色团,使它与丙烯酰氯反应,合成出含有双键的荧光素单体Ac-Flu,然后令其与丙烯酰胺共聚,制备得到含有荧光素生色团的水溶性荧光聚合物poly(Ac-Flu-co-AM)。

In this thesis, monomer with unsaturated double bond was firstly synthesized byreacting acryloyl chloride with bifunctional monomer. Such synthesized monomer ormonomer with initial unsaturated double bond was used to prepare linear polymericmaterials by free radical polymerization. A series of new degradable space polymerswith acylamino bond were subsequently synthesized using diisocyanate as thecross-linker.

本文首先通过丙烯酰氯和双官能团单体反应引入不饱和双键,或者直接使用具有不饱和双键的单体,通过自由基聚合得到含有活泼羟基或氨基的线型高分子聚合物,再用二异氰酸酯作为交联剂交联,从而合成了一系列基于酰胺键的新型可降解高分子体型聚合物。

Chapter 4: Synthesis of 1,5-diary 1-1,4-pentadien-3-ones from acetone or benzalacetone with aromatic aldehydes results in 86-97% yield with potassium hydroxide as catalyst under ultrasound irradiation in 5-60min.

为合成氰基环己醇找到一条方便高效的合成方法。第四章:研究了超声辐射下,以氢氧化钾为催化剂,芳香醛与丙酮及亚苄基丙酮之间反应合成1,5-双苄基-1,4-戊二烯-3-酮。

P-Isopropylphenol was synthesized by catalytic transfer dehydrogenation with 5% Pd/C using 4-isopropylcyclohexenone as the material and the hydrogen offer, industrial dipentene as the hydrogen acceptor and the solvent.

采用5%Pd/C作为转移氢催化剂,4-异丙基环己烯酮为氢给予剂,工业双戊烯为氢接受剂和溶剂进行反应,合成了对异丙基苯酚。

Three new ferrocenylmethyl-substituted indenes and cyclopentadienes were synthesized by the addition of hydrogen anion and carbon anion to fulvene and benzo fulvene respectively, moreover, their structures were characterized by NMR and MS.

本文以二茂铁基富烯和二茂铁基苯并富烯为前体,通过负氢和负碳对双键的加成,合成了3个新型的二茂铁基甲基取代的茚及环戊二烯,并对其结构进行了核磁及质谱表征。

In the synthesis of canthaxanthin by selective catalylitic oxidating of βcarotene,CO2 was used as acidifying or alkalizing agent,which controlled reacting system acidity and protected polyene.,producing less by-products and increasing catalylitic oxidation selectivity.In the addition reaction of isoprene with hypochloric acid,1-chloro-2-methyl-3-buten-2-ol and l-chloro-2-methyl-3-buten-4-ol were made by controlling of the acidity with carbon dioxide i...

CO2作为酸碱调节剂和惰性气体,在β-胡萝卜素催化氧化合成角黄素反应中,可以控制反应体系酸性,保护原料中的双键,减少副反应发生,提高催化氧化反应的选择性;异戊二烯氯醇化生成1-氯-2-甲基-3-丁烯-2-醇和1-氯-2-甲基-3-丁唏-4-醇反应中,CO2代替有机酸作酸碱调节剂,控制次氯酸的生成速度,达到调控反应的目的,反应条件温和,不副产固体。

Seven of them have not been reported.Their structures were confirmed by IR,~1HNMR,MS,and element analysis. 4.Meanwhile,the green methylation procedure of imides was developed by using dimethyl carbonate as methylation reagent.A series of imides,for example,phthalimide,3,4-dibromo-maleimide and succincide were used for substrates.The effects of DABCO(1,4-diazabicyclo [2.2.2]octane)and DBU(1,8-diazabicyclo[5.4.0]undec-7-ene)as a catalyst in this kind of reactions were investigated.2-Bromo-3-(1-methylindolyl-3-yl)-1-methyl-1H-pyrrole-2,5-dione was prepared by using dimethyl carbonate,which further expanded the use of dimethyl carbonate,as a green agent in organic synthesis.

在以硫酸二甲酯为甲基化试剂对3,4-二溴马来酰亚胺进行N-甲基化反应合成3,4-二溴-N-甲基马来酰亚胺的同时,以碳酸二甲酯为甲基化试剂,对3,4-二溴马来酰亚胺、邻苯二甲酰亚胺、琥珀酰亚胺等酰亚胺类化合物的N-甲基化反应进行了研究;考察了1,4-二氮杂双环[2.2.2]辛烷,1,8-二氮杂双环[5.4.0]十一碳-7-烯、碳酸钾和四丁基溴化铵等作为催化剂对碳酸二甲酯N-甲基化反应的反应时间和收率等的影响,并应用碳酸二甲酯为甲基化试剂,合成了N-甲基-3-溴-4-(1-甲基-吲哚-3)-马来酰亚胺。

A similar reaction of the sulfur analog gave only the product of tetramethylene bridged bisdititanium halides.

在企图合成硫桥环戊二烯基化合物时,得到的却是四亚甲基桥联双环戊二烯基金属衍生物。

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