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Part 2. Annulation reaction of 3, 4-dichlorocoumarin (1) and 3, 4-dichloromaleimide (8) by a new general annulation strategy developed in this group with 2-phenylbenzofuran (15), 3-phenylbenzofuran (16), 2, 5-diphenyloxazole (17), 2, 5-diphenylthiazole (18), 2-methyl-4-phenylthiazole (19) and 2, 3-dimethoxy-1, 3-butadiene (40) were investigated.

二。在本课题组前一阶段提出的从二氯代环烯酮与1,1-二芳基乙烯的光化反应以及光化反应中得到的环丁烷产物的连续电环化反应对3,4-二氯马来酰亚胺以及3,4-二氯香豆素进行增环反应的工作基础上,研究了3,4-二氯香豆素(1)和3,4-二氯马来酰亚胺(8)与5个α-苯基取代的环烯烃2-苯基苯并呋喃(15),3-苯基苯并呋喃(16),2,5-二苯基噁唑(17),2,5-二苯基噻唑(18),2-甲基-4-苯基噻唑(19),以及一个丁二烯——2,3-二甲氧基丁二烯(40)进行的芳香族增环反应。

The results have indicated that the introduction of electron-donating methoxy or electron-withdrawing cyano-group at the 7-position of 3-phenylcoumarins caused a bathochromic shift for both absorption and fluorescence spectra. The phenyl group at the 4-position derivative has a hypsochromic shift for both absorption and fluorescence spectra.

结果发现,在3-苯基香豆素的7-位引入给电子基团甲氧基或吸电子基团氰基均使它们的吸收光谱和荧光光谱产生红移,4-苯基香豆素的衍生物的吸收光谱和荧光光谱均产生蓝移。3-苯基香豆素衍生物与4-苯基香豆素的衍生物的基态和激发态的电子转移方向相反。

Methylphenyldichlorosilane is synthesized by Grignard reaction between methyltrichlorosiliane with bromobenzene.

研究发现高苯基含量的甲基苯基硅橡胶(苯基含量30mol%)具有优异的耐辐照性能,这归因于体系内存在大量的具有共轭结构的苯基基团。

The one is-2-isopropylidene-3-[1-(3,4-dimethoxyphenyl)ethyl-idene] succinic anhydride, the other is-2-isopropylidene-3-[1-(3,4-methylenedioxyphenyl)- ethylidene] succinic anhydride.

合成了三种苯基俘精酸酐,其中具有给电子基的3-(3,4-二甲氧基苯基)亚乙基(2-亚丙基)丁二酸酐与3-(3,4-亚甲二氧基苯基)亚乙基(2-亚丙基)丁二酸酐是新化合物。

A series of novel polys: poly, poly and their copolymer poly were synthesized at high temperature by nucleophilic polycondensation of bisphenol 4 (3 phenyl 4 hydroxyphenyl) 2,3 phthalazin 1 one with activated difluorodiphenylketone, dichlorodiphenylsulfone and both together.

将苯基取代类双酚化合物 4-(3 -苯基-4-羟基苯基)-2 ,3 -二氮杂萘-1 -酮与活性双卤单体如 4,4 -二氟二苯酮、4,4 -二氯二苯砜进行高温缩聚反应,合成了高分子量的新型苯基取代杂萘联苯型聚芳醚材料;用1 H NMR、FT-IR表征了类双酚单体及聚合物的结构。

Four hemicyanine derivatives,-N-(4-sulfobutyl)-4-[2-(4-N,N-dimethylamino-phenyl) etheny1] pyridinium (P1),-N-(4-sulfobutyl)-4-[2-(4-N,N-dimethylaminophenyl)-1,3-buteny1] pyridinium (P2),-N-(4-sulfobutyl)-4-2-(4-N,N-dimethylaminophenyl) ethenyll quinolinium (Q1) and-N-(4-sulfobutyl)-4-

合成了具有不同共轭链长度的吡啶盐类及喹啉盐类半菁染料-N-(4-磺酸丁基)-4-[2-4-N,N-二甲基氨基苯基)乙烯基]吡啶鎓盐(P1、-N-(4-磺酸丁基)-4-[2-4-N,N-二甲基氨基苯基)丁二烯基]吡啶鎓盐(P2、-N-(4-磺酸丁基)-4-[2-(4-N,N-二甲基氨基苯基)乙烯基]哇琳鎓盐(Q1)以及-N-(4-磺酸丁基)-4-[2-4-N,N-二甲基氨基苯基丁二烯基]喹啉鎓盐(Q2)。研究了它们的光物理性质,并将它们用作TiO2纳米晶电极的光敏化剂引入光电化学电池。

Ten novel derivatives of 1-phenyl-5-[5-(substituted anilinocarbonylmethylthio)-4-phenyl-1,2,4- triazol-3-ylmethylthio]-tetrazole were synthesized rapidly in high yields by the reaction of N--2-chloryacetanilide (3) with 1-phenyl-5-(5-mercapto-4-phenyl-1,2,4-triazol-3-ylmethylthio)-tetrazo- le (2) under microwave irradiation and phase transfer catalysis conditions.

采用微波和相转移催化法通过1-苯基-5-(4-苯基-1,2,4-三唑-5-巯基-3-甲硫基)四唑(2)与2-氯乙酰芳胺(3)反应高效、快速地合成了10种尚未见文献报道的1-苯基-5-[5--4-苯基-1,2,4-三唑-3-甲硫基]四唑。其结构经IR,1HNMR,13CNMR和元素分析表征。生物活性实验结果表明,该类化合物在较低浓度下部分化合物对小麦芽有很好的促进作用

First, the geometry optimization for 1-phenyldibenzophosphole and triphenylphosphine were carried out using quantum chemical AM1 method.

用量子化学AM1方法优化了1-苯基二苯并膦和三苯基膦的几何构型,比较了两种化合物的电子结构和空间结构,发现PDBP作为羰基合成铑膦催化剂的配体要优于三苯基膦;系统研究了PDBP的合成方法,其最佳合成条件为:在无水无氧的条件下,采用二乙胺锂与溴化四苯基膦摩尔比为3,反应温度为22 ℃,反应5 h,反应后酸化, pH值为1~2,产物收率可达到85%~88%。

A synthesis method of 2-(2'-hydroxyl-4'-benzoyloxy-phenyl)-2H-benzotriazole and derivatives thereof is provided, and is characterized in that 2-(2', 4'-dihydroxyphenyl)-5-X-2H-benzotriazole and benzoyl chloride are taken as raw materials for reaction in solvent for 1-8 hours under the temperature of 50-140 DEC C with the mole ratio of 1 to 0.95-1.1, wherein, the amount of the solvent is 2 to 20 times that of the 2-(2', 4'-dihydroxyphenyl)-5-X-2H-benzotriazole and X represents H, F, Cl, Br.

一种2-(2′-羟基-4′-苯甲酸基苯基)-2H-苯并三唑及其衍生物的合成方法,其特征是,以2-(2′,4′-二羟基苯基)-5-X-2H-苯并三唑和苯甲酰氯为原料,在溶剂中进行反应,反应温度50℃~140℃,反应时间1~8小时,反应原料摩尔比2-(2′,4′-二羟基苯基)-5-X-2H-苯并三唑∶苯甲酰氯为1∶0.95~1.1,溶剂用量为2-(2′,4′-二羟基苯基)-5-X-2H-苯并三唑重量的2~20倍,其中X代表H、F、Cl、Br,具有反应条件温和、反应收率高和产物纯度高的特点。

Two chiral stationary phases, phenyl isocyanate teicoplanin CSP and 3,5-dimethylphenyl isocyanate teicoplanin CSP were prepared from the macrocyclic glycopeptide teicoplanin CSP using derivative agents, phenyl isocyanate or 3,5-dimethylphenyl isocyanate, respectively.

用大环抗生素替考拉宁手性固定相分别与3,5-二甲基苯基异氰酸酯和苯基异氰酸酯反应得到了两种新型的高效液相色谱手性固定相----3,5-二甲基苯基异氰酸酯替考拉宁手性固定相和苯基异氰酸酯替考拉宁手性固定相。

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