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In addition,α-alkenoyl ketene--acetals mainly used as the synthons of 3C and 5C, theα-functionalized reactions of which just limited on some simple reactions, as bromination, nitration, acetylation. However, the understanding of the forming of C-C bond atα-position is far from enough.

另外,对于α-烯酰基二硫缩烯酮的研究则主要集中在其作为3C或5C合成子的研究上,其α-位的官能化研究只是停留在溴化、硝化、脱羧等简单的反应之上,而对α-位C-C键的形成还缺乏足够的认识。

According to the result, we believed that the reason resulted in the low sensitivity was that the marker residue compound MQCA structure has changed after conjugated with protein and the antibody induced by the conjugation could not recognize the free MQCA in the ci-ELISA. Therefore we designed some hapten which could reserve the marker residue structural speciality mostly. After synthesis route selection and optimum, the hapten 7-Hydroxymethyl-3-methyl-quinoxaline-2-carboxylic acid was synthesized, used 4-methyl-2-nitroaniline as the start material via six steps, such as oxidation cyclization, bromize reaction, hydrolysis, Beirut reaction, reduction, hydrolysis. This work established basis for producing the high affinity antibody and developing the sensitive ELISA residue detection method.

本论文认为导致ELISA检测灵敏度较低的原因,是残留标示物和蛋白偶联后的特征结构发生改变,诱导产生的抗体不能够对游离MQCA很好的识别,因此,本论文设计了能够最大化保留MQCA结构特征的系列半抗原结构,并对其合成路线进行了筛选和优化,最终以对甲基邻硝基苯胺为起始原料,经氧化环化、溴代、水解、Beirut缩合、还原、水解六步反应制备含羟甲基结构的MQCA衍生物7-羟基甲基-3-甲基-喹噁啉-2-羧酸,为制备对游离残留标示物高亲和力的抗体,高灵敏度的ELISA残留检测方法的建立奠定基础。

Analyse and compare what adopt a variety of pair of methods, the Michael addition reaction of ester of acerbity second of second of hydroxyl of protection of benzyl of the response of close nucleus addition that uses second nitrile and ester of formic acid second certainly, chloridize, cyanogen, reaction that take off carboxyl generates 3- benzyl oxygen radical the fifth of the ten Heavenly Stem the method of 2 nitrile, detailed discussion the action that wait and the by-product that arise possibly reach the reactant in each pace reaction, activator, dissolvent avoid a method.

通过对多种方法的分析和比较,确定采用乙腈和甲酸乙酯的亲核加成反应、氯化苄保护羟基、氰乙酸乙酯的Michael加成反应、脱羧反应生成3-苄氧基戊二腈的方法,并具体的讨论了每一步反应中反应物、催化剂、溶剂等的功能和可能产生的副产物及避免方法。

The results of magnesium and calcium ions tolerance test indicated that the modified SPS, synthesized from the above two methods,has good chelation with magnesium and calcium ions for the crablike carboxyl and ester group and increase the reaction weight with magnesium and calcium ions for addition of hydrophilic group.Both of the two modified petroleum sulfonates could produce ultra-low interfacial tension at calcium and magnesium ions concentration lower than 600 mg/L,whereas the general petroleum sulfonates could only produce ultra-low value below 300 mg/L.

耐钙镁离子能力测试结果,以大庆炼化公司两种渣油为原料,采用上述两种合成方法制备的改性石油磺酸钠,由于产物中引入蟹爪状羧酯基,对钙镁离子有较强的螯合作用,同时增加了亲水基,增大了表面活性剂分子与钙镁离子的反应量,因而在600mg/L的钙镁离子溶液中获得10-3级的超低界面张力;而普通石油磺酸钠仅能在300mg/L的钙镁离子溶液中获得超低界面张力。

In the thesis, a series of novel single and multi-armed oxadiazole bridging ligands and pyridyl-4, 5-imidazole dicarboxylic acid ligands have been synthesized. The coordination chemistry of these novel ligands with transition metal ions was investigated. In addition, two 1, 3, 4-oxadiazole bridging ligands end-capped by chelating Schiff-base coordination sites have been designed and synthesized. The coordination chemistry based on one of the two ligands with metal ions was primarily investigated.

本文报道了一系列新颖的含1, 3, 4-Oxadiazole杂环的单臂及多臂有机配体,研究了它们与过渡金属离子的配位反应化学;合成了吡啶基-4,5-咪唑二羧酸有机配体,研究了它们在水热条件下与过渡金属离子的配位反应化学;另外,还合成了1, 3, 4-Oxadiazloe杂环桥联的双Schiff-base有机配体,初步探讨了其与过渡金属离子的配位反应化学。

Methods On same oral therapy condition,the patients in control groupwere given commmon thoracocentesis on twice a week,the patients in experimental groupwere treated by thoracic tube intubation with veinal catheter.After drainage within3days,the pleural cavity of the paˉtients in group E were injected with the compound of sodium hyaluranate,sodium carboxymethylcellulose and butyltriˉamcinolone.The patients of two groups were examined by X-ray after6months.According to the database of normal crowd chest X-ray photograph,the area of patient's photograph was drawn.The value of average gray scale in the area was gathered by image analysis system and to be compared with the value of normal side,so the gray ratio was got after correction.

在口服给药条件一致的前提下,对照组患者沿用常规每周2次间断抽液的方法;实验组采用静脉留置针持续引流的方法,3日内将胸液引流尽后注入由透明质酸钠、羧甲基纤维及丁基去炎松组成的可吸收生物活性凝胶。6个月后行胸片检查,图像分析系统根据正常人群胸片同侧拟合区域采集平均灰度值并与健侧相比,经校正后得灰度比。

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第三章汉藏语&的&字结构的类型划分。