英语人>网络例句>iodic anhydride 相关的网络例句
iodic anhydride相关的网络例句

查询词典 iodic anhydride

与 iodic anhydride 相关的网络例句 [注:此内容来源于网络,仅供参考]

Ib was synthesized by condensation of phthalic anhydride with 2-methylresorcinol in fused AlCl〓/NaCl (5∶1), followed by selective acetylation, methylation, NBS bromination and condensation with sodium ethoxide.

邻苯二甲酸酐在熔融的三氯化铝-氯化钠(5:1)中和-2,6-二羟基甲苯环合得1,3-二羟基-2-甲基蒽醌〓后经选择性乙酰化、甲基化、NBS溴化、乙醇钠缩合得1-甲氧基-2-乙氧甲基-3-羟基蒽醌。

The low phosphate scale and corrosion inhibitor consists of hydroxyl ethylidene bisphosphoric acid in 0.5-1 mg/l, hydrolyzed polymaleic anhydride in 0.5-2 mg/l and polyasparic acid in 1-2 mg/l, with the total concentration being 3 mg/l.

还含有0.5~2mg/L的水解聚马来酸酐和1~2mg/L的聚天冬氨酸,低磷阻垢缓蚀剂的总质量分数之和为3mg/L。

2A series of alternating polyamide-imideswith fluorenyl cardo structure was synthesized by "one-pot" polycondensation of cardo diamines,trimellitic anhydride and various aromatic diamines including p-phenylene diamine,m-phenylene diamine, 4,4\'-oxydianiline,3,4\'-oxydianiline,2,2-bis[4-(4-aminophenoxy)phenyl]propane, 2,2-bis[4-(3-aminophenoxy)phenyl]propane respectively using triphenyl phosphite as condensing agents.

采用&一锅法&(One—pot Synthesis),由Cardo二胺、偏苯三酸酐和不同二胺包括对苯二胺、间苯二胺、4,4\'—二氨基二苯醚、3,4\'—二氨基二苯醚、2,2—双[4—(4—氨基苯氧基苯基]丙烷和2,2—双[4—(3—氨基苯氧基)苯基]丙烷合成了一系列含有芴基Cardo结构的交替聚酰胺酰亚胺。

2A series of alternating polyamide-imideswith fluorenyl cardo structure was synthesized by "one-pot" polycondensation of cardo diamines,trimellitic anhydride and various aromatic diamines including p-phenylene diamine,m-phenylene diamine, 4,4\'-oxydianiline,3,4\'-oxydianiline,2,2-bis[4-(4-aminophenoxy)phenyl]propane, 2,2-bis[4-(3-aminophenoxy)phenyl]propane respectively using triphenyl phosphite as condensing agents.

采用&一锅法&O(来源:88AB57C论文网www.abclunwen.comne—pot Synthesis,由Cardo二胺、偏苯三酸酐和不同二胺包括对苯二胺、间苯二胺、4,4\'—二氨基二苯醚、3,4\'—二氨基二苯醚、2,2—双[4—(4—氨基苯氧基苯基]丙烷和2,2—双[4—(3—氨基苯氧基)苯基]丙烷合成了一系列含有芴基Cardo结构的交替聚酰胺酰亚胺。

The process comprises the subsequent steps a through e: a reacting phthalic anhydride with fluorobenzene or a derivative thereof in appropriate reaction conditions; b over reducing the product obtained in step a at the ketone moiety; c reducing the product obtained in step b with sodium dihydro-bis (2- 15 methoxyethoxy) aluminate to the corresponding alcohol ; d chlorinat ing the alcohol obtained in step c ; e inserting CO into the product obtained in step d through an appropriate Pd-containing catalytic system.

该方法包括以下步骤a~e:a使邻苯二甲酸酐与氟苯或者其衍生物在适当的反应条件中反应;b完全还原步骤a中获得的产品的酮部分;c用二氢-二(2-甲氧基乙氧基)铝酸钠将步骤b中获得的产品还原成相应的醇;d对步骤c中获得的醇进行氯化;e通过适当的含Pd的催化剂体系,将CO插入到步骤d中获得的产品中。

The presence ofelectron donor(methoxy or methylenedioxy group) and electronacceptor anhydride group) moieties on phenyl fulgide derivativesleads to an intramolecular charge transfer upon exication that results ina solvatochromic effect.

可将苯基俘精酸酐视为由给电子基和得电子基两部分组成,分子内的电荷转移是造成正溶剂效应的主要原因。

The volume ratio of furaldehyde to acetic anhydride is 1∶2; the mole ratio of furaldehyde with anhydrous potassium carbonate is 1.00∶0.54. The best phase transfer catalyst is PEG1000, the mass ratio of PEG1000 with furaldehyde is 4.3%, the reaction time is 11 min, the reaction power of microwave is 260 W. The yield ofα-furanacrylicacid is up to 72.3% under these reaction conditions.

研究结果表明:在微波辐射功率为260 W、微波反应时间为11 min、以聚乙二醇1 000(PEG1000)为相转移催化剂,糠醛与乙酐的体积比为1∶2,糠醛与无水碳酸钾的量比为1.00∶0.55时,α-呋喃丙烯酸的产率为72.3%。

Then the fiber was transferred to a 4 mL vial which was filled with 100 μL of trifluoroacetic anhydride and stood 30 sec for headspace extraction. Afterward the fiber was transferred again to another blank 4 mL vial and stood 10 min for on-fiber derivatization before the analysis with GC/MS. The absorption-time profiles for both furoic acid and creatinine were examined.

有关尿中肌酸酐的量测,首先亦使用65μm PDMS/DVB纤维,在电磁搅拌转速1200rpm下以直接样本接触方式吸附60秒后,将已吸附肌酸酐的纤维挪至装有100μL无水三氟醋酸的4mL样本瓶中顶空吸附30 sec,再将纤维挪至另一个空白的样本瓶并静置10min(以利衍生物trifluoroacetamide的生成),最后再以气相层析质谱仪进行分析。

Diethyl glutarate was synthesized using glutaric anhydride and ethanol, which were separated from dicarboxylic acid, as raw material, heteropoly acid as catalyst.

以从二羧酸中分离出的戊二酸酐和乙醇为原料,用杂多酸为催化剂,合成了戊二酸二乙酯。

The diisoamyl glutarate in catalysis of silicotungsticacid was preparated by esterification of isoamyl alcohol and glutaric anhydride seperated from dicarboxylic acid.

用硅钨杂多酸为催化剂,以从二羧酸中分离出的戊二酸酐和异戊醇为原料合成了戊二酸二异戊酯。

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