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Methylpyridine-coordinated ruthenium benzylidene complex 62 shows thehighest catalytic activity. TOF=960 h~(-1) is achieved during RCM reaction of 50, TOF=4 h~(-1)is obtained during the CM reaction of acrylonitrile with 1-decene.

其中,2-甲基吡啶配位的钌卡宾配合物62的催化活性最高,在催化烯烃50闭环交互置换反应时TOF可达960 h~(-1);催化丙烯腈与1-癸烯交叉交互置换反应时TOF达到4 h~(-1)。

Based on studies of RCM reaction of 50 and CM reaction ofacrylonitrile with 1-octene or 1-decene catalyzed by pyridine derivative-coordinatedruthenium benzylidene complexes, it can be concluded that ruthenium benzylidene complexwith the more labile dissociating ligand exhibits the higher initial activity and better catalyticperformance.

吡啶衍生物配位的钌卡宾配合物催化含氰基烯烃50闭环交互置换反应和丙烯腈与1-辛烯、1-癸烯交叉交互置换反应表明,催化剂中吡啶衍生物配体越易解离,其初活性越高,催化活性越好。

Aroma components of Hexylalcohol,Benzeneethanol,Butylalcohol,Pentylalcohol, ethyl acetate, Lactic acid ethylester, Butanedioic acid,diethylester, isopentylacohol acetate, acetic acid hexylester, acetic acid phenethylester, hexanoic acid ethylester, ethyl caprylate, decanoic acid ethylester, octanoic acid, linalool andα-terpineol were identified in former kiwi wine reports.

本试验首次在猕猴桃酒中发现了油酸乙酯,棕榈酸乙酯,9-癸烯酸,肉豆蔻酸乙酯,月桂酸乙酯,香茅醇,法呢醇,异薄荷酮香气物质,目前国内外资料中报道的猕猴桃酒香气物质—己醇,苯乙醇,丁醇,戊醇,乙酸乙酯,乳酸乙酯,琥珀酸二乙酯,乙酸异戊酯,乙酸己酯,乙酸苯乙酯,己酸乙酯,辛酸乙酯,癸酸乙酯,辛酸,芳樟醇,α-松油醇等均在本试验研究中也检测出,并得到证实。

The polymerization of decene to prepare synthetic lube base oil over AlCl3/TiCl4 catalyst was studied.

以AlCl3/TiCl4为催化剂对癸烯聚合制润滑油基础油进行了研究。

Test results showed that AlCl3/TiCl4 catalyst was the preferred catalyst system for polymerization of decene to prepare PAO.

结果表明,癸烯聚合制备PAO,AlCl3/TiCl4是较适宜的催化剂。

More than 75%of dodecene,decene,allylplenylether,phenylpropene(1.9×10-3mol) were completely hydrosilylated with 23.2 mg complex containing 4.9×10-6 mol platinum within 0.75 hour.

使用23.2 mg络合物(含4.9×10-6 mol Pt)为催化剂、分别使用1.9×10-3 mol 1-十二烯、癸烯、烯丙基苯基醚、苯丙烯进行硅氢加成反应,在0.75 h内产率超过75%。

SM6 and SM7 of uncrystal were analyzed through GC-MS, the results showedthat SM6 main contained unsaturated fatty aldehyde with fragrance, i.e.-2,4-decadienal(58%), tetradecanoic acid (55.78%), 2-decenal(50%), Phthalic acid isobutylundecyl ester(47%), 2, 4-Decadienal(41%), 2-Undecenal (31%), 2-Methyl-Z,Z-3, 13-octadecadi-enol(18.84%), and SM7 contained saturation alkanes, i.e. 1, 2-Benzenedicarboxylic acid, butyl cyclohexyl ester(23.90%), Triacontane(22.63%),Nonacosane(21.04%), Heptadecane(18.84%), Octacosane(13.58%). Toxicological experiments were done to insure the pigment safety.

并对紫红丝膜菌色素非晶体部分的黄色油状物SM6和紫色粉末物SM7作了GC-MS分析,结果显示SM6中主要为具有香气成分的不饱和脂肪醛,其中含量较高的依次为:-2,4-癸二烯醛(58%)、十四烷酸(55.78%)、2-癸烯醛(50%)、邻苯二甲酸异丁基十一烷酯(47%)、2,4-癸二烯(41%)、2-十一碳烯醛(31%)、2-甲基-Z,Z-3,13-十八碳二烯酸(18.45%)等;SM7中主要为饱和直链烷烃,其中含量较高的依次为:1,2-苯二羧酸丁基环己酯(23.90%)、三十烷(22.63%)、二十九烷(21.04%)、十七烷(18.84%)、二十八烷(13.58%)。

Was applied to the AD reaction of eight olefins in PEG/NMO system according to the protocol of ligand 8. The yields and ees of the diols were 70~90% and 77~96%(except for trans-5-decene and ally naphthyl ether) respectively.

在与8相同的催化反应条件下,手性配体9催化八种烯烃的AD反应得到的化学产率和ee值分别为70~90%和77-96%(反式-5-癸烯和萘基烯丙基醚除外)。

The yields were 67~89% and 61~90% respectively, and the ees were 66~99. 9% and 68~99. 9% respectively (except for trans-5-decene and ally naphthyl ether). With trans-stilbene as the substrate, chiral ligands and OsO〓 could be recovered and reused five times in the AD reaction with high catalytic activity and stereoselectivity.

4在PF〓/NMO体系中,将配体8和10分别用于八种烯烃的AD反应,配体、OsO〓和底物的摩尔比为0.02/0.015/1时,化学产率分别为67~91%和61~90%,ee值分别为66~99.9%和68~99.9%(反式-5-癸烯和萘基烯丙基醚除外)。

The results of AD reactions are as follows:(1) When the AD reaction of eight olefins was performed at 0.5mo1% OsO〓 and 2mol% ligand 8 in PEG/NMO system, the diols were obtained in 78~90% yields and 78~96% ees (except for trans-5-decene and ally naphthyl ether).

催化结果如下:(1)在PEG/NMO体系中,将配体8用于八种烯烃的AD反应,配体、OsO〓和底物的摩尔比为0.02/0.005/1时,化学产率为78~90%,除反式-5-癸烯和萘基烯丙基醚较低外,其它六种烯烃的相应二醇产物的ee值为78~96%。

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