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In this thesis the planar bilayer lipid membranes inlaid with oxide cholesterol , phosphatidylcholine or cephalin have been prepared .The effects of membranes formulas on membranes stability and zinc ions transfer ability have also been studied.

中文摘要采用氧化胆固醇与磷脂混合作为成膜液制备双分子层脂质膜的方法,研究了制备平板双分子层脂质膜的配方和成膜条件,并对制得的双分子层脂质膜的稳定性、离子通透性、离子选择通过性能、双层膜中氧化胆固醇对通透性的影响等进行了研究。

After analyzing glutinous rice waxy gene sequence reported by previous studies, two pairs of dominant and codominant STS molecular markers based PCR were designed for distinguishing glutinous rice, according to the distinctions between glutinous rice wx gene and nonglutinous rice Wx gene. Moreover, the whole sequences of the two Wx genes of nonglutinous rice reported by others were also aligned, and another two pairs of dominant STS molecular markers were designed to discriminate Wxa from Wxb based on the special site between the two genotypes. Then, corresponding rice genotypes were identified by the established new markers.

通过对前人公布的糯性水稻蜡质基因全序列测定结果的分析,根据糯性水稻与非糯性水稻蜡质基因序列位点的差异,设计了两个基于PCR扩增反应的可特异识别糯性水稻的显性和共显性STS分子标记;同时在前人公布的非糯性水稻蜡质基因的不同类型的全序列比对分析的基础上,选取了两种基因型特定的差异位点,设计了两个基于PCR扩增反应用于特异识别这两种Wx基因的显性STS分子标记,并用新建立的标记对相应的水稻基因型进行了检测。

The synthesis of the pentacyclic skeleton of Et-743 and the construction of the five chiral centers thereof.1. The core pentacyclic skeleton of phthalascidin was constructed with L-dopa as the starting material via thirteen steps. First, two basic synthons, the C-1 functionalized tetrahydroisoquinoline compounds 8 and N-protected Z-dopa derivative 9, were prepared from L-dopa. They were coupled via amide bond to form the dipeptide compounds 10, which were the first key intermediates. Then the primary hydroxyl groups were transformed into the corresponding amino aldehydes 11 via Swern oxidation. Followed by the intramolecular Pictet-Spengler cyclization, the pentacyclic compounds 12 were synthesized.

五环骨架的构建及五个正确手性中心的确立:1.1我们以L-多巴为起始原料,经过多步官能团保护和转化合成了基本结构单元8然后和苯丙氨酸衍生物9,通过缩合反应生成酰胺中间体10,经Swern氧化得到醛化合物11,然后再次利用分子内改良的Pictet-Spengler反应一步构建c,d两环,得到五环骨架化合物12,最后,实现了21-位羰基向氰基的转化,得到了C-1位官能化的化合物14,化合物14不但具有和Et-743一致的五环骨架,而且分子中五个手性中心立体构型也与其完全相同:其中,3,位和13,位的手性中心由原料L-多巴带入,而1,位,11,位和21,位手性中心则通过不对称诱导而确立。

Thus, a topological rubber glove is ofsuch a structure that is topological achiral and has topological point group 〓 in 〓space.

我们的结果表明:具有拓扑点群〓的分子是拓扑手性的;具有拓扑点群〓的分子是拓扑非手性的;如果一个分子在三维空间具有拓扑点群〓,那么这个分子具有拓扑橡胶手套的性质。

The minimal energy conformations of host-guest complexes were obtained with Tripos force field. Molecular dynamics simulations were carried out to investigate chiral molecular recognition and the distribution of hydrogen bonds. The energies of recognition system were calculated with MM+ force field as well.

首次将分子力学方法引入卟啉的手性分子识别领域的研究;用Tripos力场研究了主客体配合物最低能量构象,比较了同一主体与互为对映异构体的两个氨基酸甲酯形成的配合物的能量差异;用分子动力学模拟方法研究了手性分子识别行为及体系的氢键分布;用MM+力场研究了识别体系的能量。

There are three copies of R fragment in the S mt-genome, and each copy contains two closely adjacent open reading frames: orf355 and orf77. Among these three copies two BamHI fragments were cloned, and the sequence analysis showed that cox1 and cox2 gene lies upstream of the R region in each fragment, respectively. However, they locate in different strands and head to head with R. In this study, we found that:(1) The expression of cox1 and cox2 is not affected by the transcription of R region;(2) The two copies of R region transcribe in large amount in the microspores, and produce transcripts of 1.6kb and 2.8kb, respectively, in the sterile microspores; However, the abundance of these two transcripts is reduced in the fertility restored microspores, realized through the mRNA decay, and this reduction occurs at the uninucleate microspore stage;(3) In the sterile microspores, the 5 terminus of the 1.6kb transcript contains a palindrome region that can fold into a stem-loop.

本研究发现:(1) cox1和cox2的转录没有受到R区转录的影响;(2)两个拷贝的R区在在不育花粉中高丰度表达,其转录本大小分别为1.6kb和2.8kb;而在育性恢复的花粉中,这两个转录本的丰度被大大降低,进一步分析表明这一结果是通过mRNA分子的降解途径来实现的,此降解过程发生在单核花粉期;(3)在不育花粉中,1.6kb转录本的5′末端具有一段可形成茎环结构的迴文对称序列,而在可育花粉中,其5′末端短缺了9个碱基;(4)在不育花粉和育性恢复的花粉中,R区转录本的加尾位点都集中位于一个3′茎环结构之后;(5)不管是在不育花粉还是育性恢复的花粉中,orf77区域内均在第52位和100位核苷酸处发生了不同频率的C向U的编辑,从而形成UGA终止密码;(6)不管是orf55-orf77的成熟转录本还是转录前体分子,都已被加上了Poly尾巴,表明已进入降解途径;在以上实验结果的基础上,本研究对S型CMS花粉育性的恢复机理进行了如下推测:在不育花粉和育性恢复的花粉中,orf77区域内均发生了终止编辑,即由RNA编辑产生了提前终止密码子。

By comparing the amino acids sequences of SCRs of different regulators of complement activation and homologous structure units of DAF in different species, the conservative and nonconservative amino acids in DAF were determined. The possible activity sites were analysed and mutation amino acids sites to construct the mutant library were defined.3. Constructing and evaluating of yeast display mutant library on DAF scaffold.

SCRs多重序列比较及DAF突变位点的选择通过对补体调控蛋白家族成员、不同种属DAF分子的同源结构单位SCR的氨基酸序列进行多重序列比较,确定了DAF分子中的保守性氨基酸和非保守性氨基酸,并根据已有的实验结果,对DAF分子可能活性位点进行了分析,确定了构建酵母细胞表面呈现库的突变氨基酸位点。

In the area of selective catalysis, they will soon publish the first examples of stereochemically thoroughly investigated Enantioselective Organo-Autocatalysis, a process that demonstrates conceptually new catalysis design strategy and also provides structurally well-defined small-molecule models that may help explain the origin and maintenance of homochirality fundamental to the functions of biological systems.

在相邻的选择性催化领域,他们即将发表设计发现的首例有机小分子催化的高立体选择性自复制过程(Enantioselective Organo-Autocatalysis),此类反应不仅避免了繁琐的催化剂和产物分离问题,更有意义的是充分利用了产物自身的催化功能,并为分子手性单一性这一生命体根本特征的起源和自发维持提供了第一个简洁的小分子模型系统。

The sizes of the self-assembly micelles of the amphiphilic block copolymers and the effects werestudied by dynamic light scattering and UV-visible spectrophotometer. The micelle sizes werelargely influenced bythe hydrophobic chain content in the copolymer, the properties of the solvent and the copolymer concentration in the organic phase. The morphology of the micelles was investigated by transmission electron microscopy. Theresults showed that the micelles appeared spheres with inner core and outer shell. The critical association concentrations were determined by pyrene monomer fluorescence probe technology. The degradability of copolymer was studied by the loss of the intrinsic viscosity in the degradation process. The results indicated that the degradation rate of PECL was slower thanthat of PELLA and PEDLLA. The stability of the copolymer micelle dispersion was examined by measuring the critical flocculation concentration, which gradually decreased with increasing the content of thehydrophobic chain in the copolymer. The rheological results showed thatthe viscosity ofthe micelle dispersion with higher content of PEG segments was firstly decreased and then increased with the increasingthe temperature. Otherwise, the variation of viscosity was irregular. The viscosity of the micelle dispersion increased with the increase of the electrolyte (Na 2SO 4) concentrations. Polymer micelles paclitaxel was prepared by self-emulsification/solvent evaporation method and solid dispersion technique with amphiphilic block polymers as the carrier material.

运用动态光散射和紫外分光光度计研究了两亲性嵌段共聚物自组装胶束的粒径及其影响因素,结果表明,自组装胶束的形成机理受制备方式的控制,胶束的粒径随着共聚物相对分子质量或疏水嵌段相对分子质量和有机相中共聚物浓度的增大而增大,随着有机溶剂的水溶性的增强而减小;采用透射电镜观察胶束的形态结构,发现胶束呈具有核壳结构的均匀球形;采用芘荧光探针法测两亲性嵌段共聚物的临界聚集浓度;通过降解过程中共聚物特性粘度的变化研究两亲性共聚物的降解性能,发现与PELLA和PEDLLA的相比,PECL 降解速率较慢;随着共聚物中疏水嵌段含量的增大,纳米分散液的稳定性逐渐下降;PEG含量高的PEDLLA纳米分散液随着温度的升高,纳米分散液的粘度先下降然后增大,反之,没有规律性,且随着电解质Na 2SO 4浓度的增大,体系粘度增大。

Therefore, the EL spectra of (Znq_2)_4 is wider than that of Znq_2. 4._2 was synthesized. The analysis of molecular spatial structure and the characterization of material performance of_2 and Liq showed that two Liq molecules and two Naq molecules were connected by Na-O-Na bond bridges to form_2. Compared with Liq,_2 exhibits stronger rigidity in planar molecular structure, larger steric hindrance and intermolecular distance, and much smaller molecular polarity, thus resulting in much longer fluorescence lifetime, much higher fluorescence quantum efficiency, wider energy bandgap and better film formability. When used as light-emitting layer in OLED,_2 shows lower formation probability of excited dimmer and exciplex formation than Liq, thus emits bluer light with higher current efficiency than Liq. When_2 ultrathin film is used as electron injection layer in OLED, it exhibits higher current density, higher luminance, lower turn-on voltage and higher current efficiency than Liq ultrathin film for the existence of sodium ions in_2 ultrathin film. 5. The summarization the relationship between molecular spatial structure and material performance of Alq_3,(Znq_2) and Liq, lead the conclusion that the molecular spatial structure of Mq_n affects its material performance in such aspects as the rigidity of planar molecular structure, intermolecular interaction, molecule stacking mode and intermolecular distance.

制备了_2,通过对_2和Liq的分子空间结构与性能进行分析与讨论,发现_2是通过两个Na-O-Na键桥将两个Liq和两个Naq连接构成的,其分子平面结构的刚性程度强于Liq,空间位阻大于Liq,分子之间的距离大于Liq,分子极性远远小于Liq;_2的荧光寿命长于Liq,荧光量子效率高于Liq,成膜性优于Liq;_2的禁带宽度比Liq大,光致发光光谱中_2的最大发射峰较Liq发生蓝移;当_2在OLED中作为发光层时,激发二聚体与激基复合物的生成几率远远小于Liq,发的光比Liq更蓝,电流效率大于Liq;_2超薄膜中有Na离子的存在,与Liq超薄膜相比,当其在OLED中作为电子注入层时,具有更大的电流密度,更高的发光强度,更低的阈值电压和更高的电流效率 5、对上述Alq_3、Znq_2和Liq的分子空间结构与材料性能之间的关系进行了归纳总结,认为Mq_n的分子空间结构主要在分子平面结构的刚性程度,相邻分子之间的相互作用,分子堆叠的方式和分子之间的距离这四个方面影响其性能。

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