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CA-CTSs including N,O-carboxymethyl chitosan,N,O-1-carboxyethyl chitosan (N,O-1-CEC),N,O-2-carboxyethyl chltosan(N,O-2-CEC),N-carboxymethyl chitosan and N-1-carboxyethyl chitosan(N-1-CEC) are quaternized using active quaternary salts prepared in laboratory.5 series including 25 kinds amphoteric chitosans characterized with polymeric ampholyte,in which 24 kinds are synthesized firstly,are obtained, 2-Hydroxypropyl dimethylbenzyl ammonium N,O-(1-carboxyethyl) chitosan chloride (GDMBA-N,O-1-CEC) is hydrolyzed into serial low molecular weight GDMBA-N, O-1-CEC with acid as catalyst and microwave as assistant instrumentality innovately.

以合成的活性季铵盐改性了N,O-羧甲基壳聚糖、N,O-1-羧乙基壳聚糖(N,O-1-CEC)、N,O-2-羧乙基壳聚糖(N,O-2-CEC)、N-羧甲基壳聚糖和N-1-羧乙基壳聚糖(N-1-CEC)等羧烷基壳聚糖,得到5个系列25种具有两性高分子电解质特征的新季铵化羧烷基壳聚糖,其中24种为首次合成;创新提出以微波辅助酸催化的方法催化2-羟丙基二甲基苄基-N,O-(1-羧乙基)壳聚糖氯化铵(GDMBA-N,O-1-CEC)水解,得到了低分子量的GDMBA-N,O-1-CEC。

Two kinds of water-soluble biomimetic chitosan derivatives with a phosphoramide linkage between glucosamine and choline were prepared through Atherton-Todd reaction under the mild conditions, including zwitterionic phosphorylcholine bound chitosan and acetyl-phosphorylcholine bound chitosan with positive charge. The interaction between chitosan derivatives and calf thymus DNA were inversigated by UV alsorption spectra and circular dichroism spectra.

采用Antherton-Todd反应制备了两种水溶性的磷酰化壳聚糖仿生衍生物:两性的N-磷酸胆碱磷酰化壳聚糖和带正电荷的N-乙基磷酸胆碱磷酰化壳聚糖,并用紫外吸收光谱和圆二色光谱研究了两种胆碱磷酰化壳聚糖衍生物与小牛胸腺DNA的相互作用。

Antioxidant 2,2′-methylene-bis(4-ethyl-6-tert-butylphenol) is synthesized by condensation of formalin and 4-ethyl-2-tert-butylphenol which is prepared by alkylation of p-ethylphenol with isobutylene in the presence of phosphoric acid or ion-exchange resin as catalysts.

研究了以对乙基苯酚、叔丁醇为原料,在酸性条件下,进行烷基化反应,合成2 叔丁基 4 乙基苯酚,再进一步缩合成抗氧剂425的工艺条件。

The pure isomers 3-(1-hydroxyethyl)-8-vinyldeuteroporphyrin Ⅸ and 3-vinyl-8-(1-hydroxyethyl)deuteroporphyrin Ⅸ were obtained from protoporphyrin Ⅸ dimethyl ester.Starting from these two acetylating compounds,eight new porphyrin derivatives were synthesized through an alkyloxy fission reaction.

以原卟啉Ⅸ二甲酯为起始原料,合成并分离得到3-(1-羟乙基)-8-乙烯基次卟啉Ⅸ(Ⅱ1)和3-乙烯基-8-(1-羟乙基)次卟啉Ⅸ(Ⅱ2)二个异构体,两者分别经酰化后与醇进行烷氧裂解反应合成了8个全新的卟啉衍生物。

By comparing the dehydration methods of three catalytic esterification reactions and the catalysts used under negative pressure, the better method of synthesizing 2 ethylhexyl chloroacetate is using stannous oxide as catalyst under negative pressure.

通过对三种催化酯化反应的脱水方法及负压下使用不同催化剂的比较和选择,提出了以氧化亚锡为催化剂负压脱水合成氯乙酸2乙基己酯的方法。

Three novel hemicyanine derivatives,-N-(4-sulfopropyl)-4-[2-(4- N, N-diethylaminophenyl)-ethenyl]pyridinium,-N-(4-suMbbutyl)- 4-[2-(4-N, N-diethylaminophenyl)ethenyl]pyridinium (EPS4), and-N-(4- su)fobutyl-4-[2-(4-N, N-diethylaminophenyl)ethenyl]quinolinium (EQS4) with different length of alkyl chains between the adsorbing group (RSO3-) and the chromophore group, were synthesized and their photophysical and photoelectrochemical properties were studied.

设计合成了具有不同空间位阻的吡啶盐类和喹啉盐类半菁染料-N-(4—磺酸根丙基)-4-[2-4(4-N,N-二乙基氨基苯基)乙烯基]吡啶鎓盐,-N-4-磺酸根丁基)-4-[2-(4-N,N-二乙氨基苯基)乙烯基]吡啶鎓盐(EPS4)和-N-(4-磺酸根丁基)-4-2-(4-N,N-二乙基氨基苯基)喹啉鎓盐(EQS4),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中。

Total mercury and methyl mercury concentrations were analyzed by cold vapor atomic fluorescence spectrometry and aqueous phase ethylation,GC separation,and CVAFS detection.

2006年1~12月,每月采集乌江流域梯级水库入出库河流水样,用两次金汞齐-冷原子荧光光谱法和蒸馏-乙基化结合GCCVAFS法测定了水中总汞和甲基汞的浓度。

The related feature of tribromide quaternary ammonium salt as selective bromide reagent was investigated by the reaction of acetophanone, propanone, phenol with self-made benzyl triethyl tribromide quaternary ammonium salt.

首次通过自制的苄基三乙基三溴季铵盐与苯乙酮、丙酮、苯酚等的反应,研究了三溴季铵盐作为选择性溴化剂的相关性能。

The synthesis of alkylcyclohexylbenzoic acid: take the synthesis of ethylcyclohexylbenzoic acid as a typical example. With the AlCl3 as the catalyst, cis+trans acetylcyclohexylbenzene is synthesized from the reaction of acetyl chloride, cyclohexene and benzene.

烷基环己基苯甲酸的合成研究:主要研究了乙基环己基苯甲酸的合成,以乙酰氯、环己烯、苯为原料,三氯化铝为催化剂,合成乙酰基环己基苯,用水合肼、氢氧化钾、一缩二乙二醇经过高温加热还原羰基(Wolff-黄鸣龙还原),将所得到的乙基环己基苯用乙酰氯进行傅克酰基化得到乙基环己基苯乙酮,所得中间体经过处理之后直接得到反式产物,将反式异构体的乙酰基氧化得到反式烷基环己基苯甲酸。

The optimal operation condition of Friedel-Crafts acylation for product Ⅰ was determined by orthogonal experiment: 0.02mol N-ethyl- carbazol, n Benzoyl chloride/n N-ethyl- carbazol=1.2, n AlCl3/n N-ethyl- carbazol=1.2 , at 25 oC for 3.5h. The yield was 94.6%.

通过正交设计实验,探讨了产物Ⅰ的Friedel-Crafts 酰化的最佳反应条件:N-乙基咔唑为0.02mol时,反应物苯甲酰氯与N-乙基咔唑摩尔配比为1.2。,催化剂AlCl3与N-乙基咔唑摩尔配比为1.2, 25℃下反应3.5h,产率可达94.6%。

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