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环戊烯

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The effect of cyclopentene concentration palladium salts, FePc, acid and reaction mechanism were discussed.

在乙腈的酸性水溶液中,考察了 Pd Ac2 /Fe Pc催化氧化环戊烯合成环戊酮的催化活性,讨论了影响该反应活性的因素及其反应机理。

A novel one-step green process for synthesis of glutaric acid by selective oxidation of cyclopentene was investigated.

研究了以环戊烯为原料、草酸为有机络合剂、H2O2为氧化剂,在催化剂钨酸(H2WO4)的作用下一步合成戊二酸的绿色新过程,考察了氧化剂的含量、反应物配比、催化剂用量、反应温度、反应时间等对反应的影响。

The present invention belongs to the field of chemical technology, and is a kind of supported tungstic acid catalyst for multiphase catalytic oxidation and synthesis of glutar aldehyde from cyclopentene.

本发明属于化工技术领域,是一种新型的环戊烯多相催化氧化合成戊二醛的负载型钨酸催化剂。

To enable the fabrication of thermally stable ultralow dielectric constant film, specific precursor materials are used, such as, cyclic siloxanes and organic molecules containing ring structures, for instance, tetramethylcycloterasiloxane and cyclopentene oxide.

为了能够制造热稳定超低介电常数材料,使用特定的前驱物材料,例如环硅氧烷和例如四甲基环四硅氧烷和环戊烯氧化物这样包含环状结构的有机分子。

Using W-HMS molecular sieve synthesized from the tungsten source of (NH4) 2WO4 as catalyst and hydrogen peroxide as oxidant, the effects of reaction time, temperature, dosage of catalyst, solvent type and volume, and oxidant concentration on the catalytic oxidation of cyclopentene to glutaraldehyde were investigated.

对以(NH4)2WO4为钨源合成的W-HMS分子筛为催化剂,过氧化氢为氧化剂,环戊烯合成戊二醛的多相催化反应进行了研究,考察反应时间、反应温度、催化剂用量、溶剂种类和用量以及氧化剂浓度等因素对戊二醛收率的影响。

To enable the fabrication of a thermally stable ultralow dielectric constant film, specific precursor materials are used, such as, silane derivatives, for instance, diethoxymethylsilane and organic molecules, for instance, bicycloheptadiene and cyclopentene oxide.

为了制造热稳定的超低介电常数膜,使用特殊的前体材料,如硅烷衍生物例如二乙氧基甲基硅烷和有机分子例如双环庚二烯和环戊烯氧化物。

Under the optimum conditions of a cyclopentene amount of 1.0 mol, a molar ratio of cyclopentene to water of 0.25, a reaction temperature of 120 ℃, a reaction time of 4.0 h, a main catalyst dosage of 4.0 g and a cocatalyst dosage of 0.8 g, the yield of cyclopentanol reached 68.6%.

确定适宜的反应条件为:环戊烯1.0 mol,n﹕n=1﹕4,反应温度120 ℃,反应时间4.0 h,硅胶负载铌酸主催化剂用量4.0 g,三(3,6-二氧杂庚基)胺助催化剂0.8 g。在此反应条件下,环戊醇收率68.6%。

Cyclopentanol was synthesized from cyclopentene and water through hydration reaction using HNb3O8·H2O/SiO2 as main catalyst and tris(dioxa-3,6-heptyl)amine (TDA-1) as cocatalyst.

在以硅胶负载铌酸为主催化剂、三(3,6-二氧杂庚基)胺为助催化剂的作用下,以环戊烯和水为原料,通过水合加成反应合成了环戊醇。

That 1,4-addition reactions of Grignard agent made from 1-bromo-3-triphenylmethoxyl-1-octene and organozinc agent made from 1-iodo-3-trimethysiloxy-1-octene with 2-(6-methoxylcarbonylhexyl)-4-(2- tetrahydro-pyranyloxy)-2-cyclopentenone both gave prostaglandin 〓 methyl ester statethat prostaglandin E compounds can be prepared by 1,4-addition reaction oforganozinc agent.

最后,研究了溴化-3-三苯甲氧基-1-辛烯基镁和碘化-3-三甲硅氧基-1-辛烯基锌与2-(6-甲氧羰己基)-4-(2-四氢吡喃氧基)-2-环戊烯酮通过1,4-加成反应合成〓甲酯的方法,结果表明,用有机锌试剂通过1,4-加成反应来合成PGE类化合物是可行的。

The results show that both norbornenic and cyclopentenic double bonds are involved in the polymerization. The propagation on the NB double bond generates structural unit I by direct addition and unit II by carbocation rearrangement, respectively. Similarly, the propagation on the CP double bond produces structural unit III by direct addition and unit IV by transannular rearrangement, respectively.

结果表明, DCPD分子的降冰片烯双键和环戊烯双键均参与了聚合反应并根据不同链增长机理产生四种链结构单元:通过NB双键的链增长反应可生成直接加成结构单元I和重排结构单元II,通过CP双键的链增长反应生成直接加成结构单元III和跨环重排单元IV。

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每逢看到沃林顿那刚毅的脸,那乌黑、忧郁的眼睛,她便会相信,他一定作过不幸的爱情的受害者。

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