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group into
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  将群
     In second part we discuss following problems:1.Transfer homomorphism of group into Fuzzy homomorphis.
     第二部分首先将群同态Fuzzy 化,给出了Fuzzy 同态为单Fuzzy 同态的两个充要条件,并以(G,(?)
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     Different types of group information need to have different aggregating methods. To fully unearth and use the information resource of interval-number group information, a new method of aggregating group information under interval-number judgment matrixes from every member in the decision group into the definitive number decision information with certain reliability was put forward, and the model of computing and revising the reliable degree of the aggregated values of group information was established. Besides, the effectiveness of the method was tested by an example.
     不同类型的群信息有不同的集结方法,针对区间数判断矩阵的群信息,为了能充分挖掘和利用这类群信息的信息资源,提出了将群中各成员的区间数决策信息集结为具有一定可靠度的确定信息的方法原理,给出了这类群信息集结值可靠度的计算模型和修正流程,并通过一个算例验证了该方法的有效性.
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  群分解为
     ON WIELANDT PROBIEMS OF DECOMPOSING A GROUP INTO F-SUBGROUPS
     群分解为F-子群的Wielandt问题
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     AN ALGORITHM OF DECOMPOSING FINITE ABELIAN GROUP INTO DIRECT PRODUCTS OF P
     一个有限Abel群分解为P群直积的算法
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  “group into”译为未确定词的双语例句
     Results (1) Transfection of pEGFP-C1/U6-2 group into MCF-7 down-regulated c-myc expression level greatly at 48 h after transfection (80%);
     (2)siRNA表达载体转染MCF748h后,pEGFP-C1/U62组显著抑制胞内c-myc表达(80%);
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     And we also divided the patient group into two groups which named cardiac dilatation group and non-cardiac dilatation group according UCG 3.We applied the Pillip Sonos 5500 type Echocardiogram to measured the left ventricular fractional shortening(LVFS), ejection fraction (EF), left atrium inner diameter , left ventricular end diastolic inner diameter (LVEDD)and left ventricular end systolic inner diameter(LVESD) in patient group, descripted the shape and function change of their heart.
     3.应用Pillip 5500型超声心动仪检测全部病人心功能指标,记录左室收缩末期内径(left ventricular end systolic diameter,LVESD)、左室舒张末期内径(left ventncular end diastolic diameter,LVEDD)、左房内径(leftatrium diameter,LAD)、LVFS和EF等指标。
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     The serine residues in V-domains of 4A4 IgG antibody were activated by phenylmethylsulfonyl fluoride (PMSF), and treated by hydrogen selenide (H2Se), resulting in conversion of serine into selenocysteine(SeCys), leading catalytic group into 4A4 IgG antibody.
     4A4IgG可变区中的丝氨酸(Ser)经苯甲基磺酰氟(PMSF)活化,再用硒化氢(H2Se)处理,则Ser转变成硒代半胱氨酸(SeCys),使4A4IgG引入该催化基因。
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     To stratify diabetic group into 2 groups according to fasting blood glucose, FPG≤7.0mmol/l(the good control group),FPG>7.0mmo/l (the bad control group) ;
     并将糖尿病组按不同空腹血糖水平分为二组:FPG≤7.0mmol/l(控制良好组)及FPG>7.0mmo/l(控制不佳组);
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     Divided NI group into subgroup,there were abnormalities in amount of mature T lymphocyte and its subgroup distribution as well as the ratio of T4 and T8 including T4/T8 normality subgroup,inversion subgroup and increase subgroup.
     进一步分组统计显示,包括T4/T8正常亚组、T4/T8倒置亚组和T4/T8升高亚组的各医院感染组,均存在不同程度的T淋巴细胞分布异常和T4/T8比值异常。
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  相似匹配句对
     group
     Ⅰ组只饲喂基础日粮;
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     B.C and group D.
     B组:10例肾衰竭非透析组;
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  group into
We use the decomposition of a group into double cosets and a graph theoretic indexing scheme to derive algorithms that generalize the Cooley-Tukey FFT to arbitrary finite group.
      
TheOPS were studied by 1H- and 13C-NMR spectroscopy, GLC/mass spectrometry, and chemical modifications (mild alkalineO-deacetylation and conversion of the N-acetimidoyl group into the N-acetyl group).
      
The incorporation of an additional ionogenic group into a surfactant molecule somewhat decreases ΔGm.
      
New results concerning the Browder-Livesey groups and natural maps ofL-groups arising in index 2 inclusions of the cyclic group into the dihedral group are obtained.
      
The tetramers are united through the propionate group into ribbons, which are joined by the Ba(2) atoms into the layers.
      
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Von Knorre first suggested the use of benzidine and o-tolidine for the determination of tungsten. With the latter reagent, he succeeded also in separat- ing tungstate from phosphate. Later on, o-dianisidine and vanillylidene benzidine have been proposed as precipitants for tungstate. The optimum pH ranges for the quantitative precipitation of tungstate by means of these precipitants and tetraminodiphenyl, which have not yet been found in the literature, are: benzidine pH: 2.0-5.5 o-tolidine 2.9-4.7 o-dianisidine...

Von Knorre first suggested the use of benzidine and o-tolidine for the determination of tungsten. With the latter reagent, he succeeded also in separat- ing tungstate from phosphate. Later on, o-dianisidine and vanillylidene benzidine have been proposed as precipitants for tungstate. The optimum pH ranges for the quantitative precipitation of tungstate by means of these precipitants and tetraminodiphenyl, which have not yet been found in the literature, are: benzidine pH: 2.0-5.5 o-tolidine 2.9-4.7 o-dianisidine 2.0-4.1 vanillylidene benzidine 1.7-3.9 tetraminodiphenyl 1.7-4.8 The effect of introducing various groups into the benzidine molecule upon the tungsten precipitating property is not profound. The relation between quantitative precipitation of tungstate with benzidine and the product of concentrations of both constituents before precipitation Was studied. It is found that quantitative precipitation of tungstate ions Can be realized only when the product of concentrations of reactants before precipitation is equal to or greater than 0.8 × 10~(-5), and the moles of benzidine added must be at least equal to that of tungstate. The gravimetlic determination of tungsten by means of o-tolidine may be applied to samples containing as low as 10 mg of rungsten trioxide in 200 ml solution, if an absolute error of 0. 5 mg can be tolelxted. For larger quantities of tungsten present in sample, the absolute errors amount to only 0.1-0.2 mg. Tetraminodiphenyl may be used as a tungsten precipitant, but no advantage over benzidine Wan found in our present studies.

1.用二胺聯苯及其數種衍生物沉澱鎢酸根時,其適宜的pH範圍如下:[4,4′]二胺聯苯 pH:2.0-5.5[3,3′]二甲基[4,4′]二胺聯苯 2.9-4.7[3,3′]二甲氧基[4,4′]二胺聯苯 2.0-4.1[4]對胺聯苯氮甲烯[2]甲苯酚 1.7-3.9[3,4,3′,4′]四胺聯苯 1.7-4.8 2.用[4,4′]二胺聯苯作沉澱劑時,二胺聯苯和鎢酸根在沉澱前的濃度之乘積與後者沉澱完全與否的關係,曾加研究。 3.用[3,3′]二甲基[4,4′]二胺聯苯作沉澱劑時,能测定低至10毫克的三氧化鎢。

An attempt was made by Hodgson to introduce alkyl or aryl group into aromatic ring through the reaction between aryldiazonium chloride [(Ar N_2 Cl)_2·ZnCl_2] and Grignard reagent (RMgX). Among the reaction products, however, he found Ar·Ar, Ar·H, ArN=NAr, ArN=N·R, Ar·X present in various proportions, but no Ar·R as expected. According to the result of an recent investigation of A. N. Nesmeyanov, the thermal decom- position of aryldiazonium fluoroborate afforded aryl cation, while the diazonium salt of...

An attempt was made by Hodgson to introduce alkyl or aryl group into aromatic ring through the reaction between aryldiazonium chloride [(Ar N_2 Cl)_2·ZnCl_2] and Grignard reagent (RMgX). Among the reaction products, however, he found Ar·Ar, Ar·H, ArN=NAr, ArN=N·R, Ar·X present in various proportions, but no Ar·R as expected. According to the result of an recent investigation of A. N. Nesmeyanov, the thermal decom- position of aryldiazonium fluoroborate afforded aryl cation, while the diazonium salt of other types gave aryl radical under the same conditions. The author caused the aryl diazonium fluoroborates to react with the less reactive organo-metallic compounds, namely, ethyl mercuric chloride and diethyl mercury. In contrast to the author's expectation, no ethylaryls were found, but diaryls (Ar·Ar), aryl- chlorides (Ar·C1) and aromatic hydrocarbons (Ar·H), and diaryls, ethyl mercuric fluoroborates, aromatic hydrocarbons and free mercury were found respectively as reaction products. In each case, tar was formed in considerable amount, especially when the decomposition was carried out with diethyl mercury.

Hodgson等曾企圖利用重氮鹽的氯化鋅的複鹽與Grignard試劑反應,希望能將烴基引入芳香環;伹在反應產物中,並無所預期的芳香烴,而有不同此例的Ar·Ar,Ar·H,ArN=N·Ar,Ar·N=N·R及Ar·X。根據最近等對芳香基氟硼酸重氮鹽的研究,證明芳香基氟硼酸重氮鹽在分解時產生烴離子,而與其它重氮鹽產生烴自由基者不同。作者因此利用芳香基氟硼酸重氮鹽及較Grignard試劑的活潑性小的有機汞化合物來代替芳香基重氮鹽的氯化鋅複鹽及Grignard試劑。在反應產物中,並無乙基芳香烴存在;生成的是不同量的Ar·Ar,Ar·H,Ar·Cl等,結果與Hodgson的實驗基本上相同。

For further studying the relationships between antibacterial action and hydrogen bonding structure in compounds related to chloramphenicol, the authors have synthesized 3-(o-hydroxy-p-nitrophenyl)-2-dichloroacetamido-propanol(Ⅴ), in which hydrogen bonding possibility was eliminated by converting the carbonyl group into methylene group.

本文叙述自邻乙酰氧基-对硝基溴化苄(Ⅶ)或邻甲氧基-对硝基溴化苄开始合成氯霉素的相似化合物——3-(邻羟基-对硝基苯基)-2-二氯乙酰氨基-丙醇(V)及其有关化合物。化合物V对金色葡萄球菌及大肠杆菌均无明显的抑制作用。

 
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