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The catalyst includes: supported Ziegler-Natta catalyst of titanium halide compound and organic electron donor compound supported with MgCl2 alcoholate carrier; aluminoxane prepared with trialkyl aluminum and water; and one kind of organic electron donor, such as organosilicon compound R2Si(OCH3)2, where R is phenyl, isopropyl, isobutyl or cyclopentyl.

该催化剂包括,a一种负载型的Ziegler-Natta催化剂,即将卤钛化合物和有机给电子体化合物负载在氯化镁醇合物载体上得到的固体催化剂,b一种通过三烷基铝与水反应而制备得到的铝氧烷和c一种有机电子给体,如有机硅化合物R 2 Si(OCH 3 ) 2 ,其中R为苯基、异丙基、异丁基或环戊基。

The works in the project just done can be summarized as five respects.(1) A device was designed to fabricate the asymmetrical resonant cavities by a pendant drop. A series ARCs with variable parameters provides a valuable experimental method for investigating the characteristics of ARCs.(2) The relationship between the number of active modes and the shape parameters in an ARC was investigated. The experimental lasing threshold was compared with theoretical result, the good agreement between two shown that it was the decrease of the number of active modes in an ARC that decreased lasing threshold.(3) Dye lasing gain was used to enhance the signals of stimulated Raman scattering of the weak gain Raman modes in a circular cavity made by a pendant drop, the instantaneous SRS spectra of weak gain Raman modes in ethanol was obtained by this new method.(4) The SRS signals of minority compound in a binary chemical complex was obtained by using dye lasing gain method. The detection concentration of minority compound was reduced to an order compared with normal SRS method.(5) A cylindrical circular cavity was formed by a liquid jet, which was used to reduce the pump intensity required for laser induced plasma spectroscopy. The limit of detection of trace element in aqueous sample was greatly decreased by this new method.

我们设计并成功制作了使悬垂液滴连续变形的装置,用此装置可以方便地改变非圆对称谐振腔的几何参数,为ARCs的研究提供了一种有效的实验方法;研究了ARCs中活性模式数和变形参数间的变化规律,激光阈值的数值计算结果和激光辐射的实验结果作了比较,二者吻合的曲线说明ARCs中活性模式数量的减少是受激辐射放大阈值降低的原因;在由单元化合物构成的微型圆对称谐振腔中,首次尝试用"激光增益"增强弱增益拉曼模式的受激拉曼散射信号,获得了乙醇分子中弱增益拉曼模式的瞬态SRS光谱;在由二元混合物构成的微型圆对称谐振腔中,用染料的激光增益增强了少量化合物的SRS信号,把少量化合物的SRS信号探测浓度降低了近一个数量级,在SRS应用于瞬态过程的组份分析方面做了卓有成效的探索;用石英毛细管形成的稳定液拄构成拄形谐振腔,降低了激光诱导等离子体光谱需要的激励能量,有效地降低了水相样品的痕量元素分析极限,为LIPS应用于微量元素的化学分析开拓了一条新的技术路线。

Target compounds have been synthesized by condensation of the aromatic nucleus and amino heterocylcle with acyl isocyanates or acylisothiocyanates in absolutely anhydrous and aprotic solvent.

为了寻找高活性的农药品种,利用生物等排原理和亚结构连接法,对脲类化合物的母体结构进行了修饰,将芳氧羧酸类及吡唑环引入酰基脲母体结构中,利用酰基异氰酸酯与杂芳环胺类化合物在无水非质子溶剂中发生亲核加成反应,合成了四个系列21种新的酰基脲类目标化合物。

The constituents were extracted by some solvents. 18 constituents were isolated from Chloroform fraction by different chromatography. 15 constituents were identified by IR ,MS and NMR as follows: 3-sitosterol, P-sitosterylpalm itate,succinate acids, 1, 4-benzenediol, 1, 2-benzenediol, p-hydroxybenzaldehyde, syringaresinol, oleanolic acid, usolic acid, ethyl caffeate , Rosmarinic acid ethylster and etc. In such constituents ,nine compounds were isolated for first time from Origanum vulgare L..

牛至药材经水煮醇沉法所得浸膏,利用溶剂法和色谱法从中分离得到18个单体成分,通过IR、MS、NMR等波谱技术鉴定了其中的15个化合物,分别为β-谷甾醇(1)、β-胡萝卜苷(2)、琥珀酸(3)、对-二苯酚(4)、邻-二苯酚(5)、对羟基苯甲醛(6)、1.2-二羟基-4-异丙基-5-甲基苯(7)、新木脂素(8)、丁香脂素(9)、齐墩果酸(10)、乌苏酸(11)、4-二十六烯(12)、正二十六醇(13)、咖啡酸乙酯(14)、迷迭香酸乙酯(15)等,其中化合物3、4、5、6、7、8、9、14、15等9种化合物均为首次从该属植物中分离得到。

In this thesis, investigations focused on heteropoly acids-catalyzed C-C and C-N bond formation reactions and the synthesis of xanthenediones and acridinediones under thermal conditions are described.1.12-Phosphotungstic acid has been used as an efficient,eco-friendly,and air- and moisture-stable catalyst to promote the direct dehydrative substitution of the hydroxy group of benzylic and allylic alcohols with variousβ-dicarbonyl compounds.

本篇论文主要描述了杂多酸催化下的C-C和C-N键的生成,以及无溶剂直接加热下合成十氢氧杂蒽二酮和9-芳基十氢吖啶二酮。主要内容如下:1。在磷钨酸催化下,1,3-二羰基化合物与醇能够顺利偶合,脱除一分子的水,生成烷基化的1,3-二羰基化合物。反应在甲苯中进行时,二芳基甲醇能与各类1,3-二羰基化合物反应,成率很高;但对于1-苯乙醇,只能得到很低的产率。

A kind of compound SRBH,which was synthesized from rhodamine B, hydrazine hydrate and salicylaldehyde,and SRBH is non-fluorscent naturally.However,the fluorescent extensity of SRBH was enhanced more than hundredfold when the ion of Crwas added to acid solution, therefore SRBH can be tested for Crin acid solution.

介绍了一种化合物SRBH,由罗丹明B,水合肼和水杨醛合成,该化合物本身为非荧光性的,但是当在酸性环境下加入铬离子后,其荧光强度可以增加上百倍,因此可以用该化合物检测水溶液中的铬离子。

Previously, the strain K14 was screened with strong nematocidal activity, and a new water soluble nematocidal compound 2, 4, 6-triacetylenic octane diacid was isolated from the fermentation broth of K14 in this work. It is the first report that polyalkyne compound had nematocidal activity.

前期工作中筛选到一株对线虫活性强的食线虫菌物K14,我们对其产生的杀线虫活性化合物进行了进一步活性追踪分离,从其发酵液中分离到一个具杀线虫活性的新化合物2,4,6-三炔辛二酸,为水溶性成分,是首次报道多炔类化合物具有杀线虫作用。

Compounds were identified by means of physic-chemical property and spectral data including three new compounds: platyphyllin A (1), neochlorgeniclatone (2),(2E,6Z)-2,6-dimethyl-8-O-β-D-glucosyl-2,6-octadienoic acid (3). The known compounds included cyclic diarylheptanoids, phenylic acid, ect.

从白桦叶的水提取物中,利用各种色谱分离手段(硅胶柱色谱、聚酰胺柱色谱、凝胶柱色谱及制备薄层色谱等),分离得到28个化合物,通过理化性质及各种波谱数据(NMR,MS,IR,etc)鉴定了23个化合物的结构,其中新化合物三个:platyphyllin A(1),新绿原酸内酯(neochlorgeniclatone,2),(2E,6Z)-2,6-二甲基-8-O--2,6-辛二烯酸(2E,6Z-2,6-dimethyl-8-O-β-D-glucosyl-2,6-octadienoic acid,3。

Nevertheless, the yield of pinacol was also strongly affected by the steric environment surrounding the carbonyl group. The pinacol coupling of aromatic aldehydes has been achieved with high yields under such a condition. However, the diastereose-lectivities of pinacols were not satisfying. Unfortunately, the ketones and most aliphatic aldehydes appeared inert under the same reaction conditions.

然而, 呐偶合反应的产率受到羰基周围环境的立体位阻影响较大,在此条件下,锌粉能有效地促进芳香族醛类化合物进行水相呐偶合反应,得到的呐醇产率高,但非对映异构体选择性差,而脂肪族醛类化合物得到的呐醇产率较低,在同样的条件下,酮类化合物不能顺利进行呐偶合反应。

The logarithm difference values of partition coefficients of the compounds in butyl ether/water and in cyclohexane/water system were used for the measurement of the Lewis acidity, while the logarithm difference values of partition coefficients in trichloromethane/water and in tetrachloromethane/water system were used for the measurement of the Lewis basicity, and they were used successfully to differentiate the relative strength of Lewis acidity and basicity for 59 benzene and its derivates.

以化合物在正丁醚/水和环己烷/水溶剂体系中分配系数的对数差作为酸性指数,以其在氯仿/水和四氯化碳/水溶剂体系分配系数的对数差作为碱性指数,提出了一种新的度量有机物Lewis酸碱性的方法,按此方法成功地区分了59种苯系物Lewis酸碱性的相对强弱;并成功地将上述酸碱性指数引入定量结构—性质/活性相关研究之中,探讨了苯系物的正辛醇/水分配系数、水溶解度和土壤有机碳吸附系数等常见理化性质与其Lewis酸碱性间的相关性并建立了相应的定量模型,发现它们之间存在良好的相关性。

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