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It crystallizes in the monoclinic space group C2/c, with a=1.6953(3)nm, b=1.9241(4)nm, c=1.7760(4)nm,β=94.75(3)°. Each Gd ion is coordinated by two oxygen atoms from two different radicals NITPh(OCH3)3 and six oxygen atoms from three hfac molecules to form eight-coordinated dodecahedron geometry.

Gd离子采取八配位的模式,两个氮氧自由基作为单齿端基配体分别以氮氧基团的氧原子与Gd离子配位,三个六氟乙酰丙酮阴离子分别以两个氧原子与Gd离子配位,构成十二面体。

By means of UV-vis spectrophotometer, the complex abilities of calix [4] arene ligands with metal ions were researched, and the effect of solvent systems was discussed.

使用紫外-可见分光光度法研究了杯[4]芳烃配体与金属离子的络合性质,并考虑了溶剂对配体与金属离子配位的影响,评价了杯[4]芳烃的不同取代基对过渡金属离子及稀土离子的配位作用。

The present invention provides a multinuclear half metallocene compound in which two or more of transition metals of groups 3 to 10 on periodic table are connected through bridge ligand simultaneously containing Pi-ligand cycloalkandienyl group and Alpha-ligand functional group and its preparation, and a process for preparing styrene polymer using the compound as a catalyst.

本发明提供了一种其中的两个或更多元素周期表第3-10族过渡金属通过同时包含π-配体环烷基二烯基团和α-配体功能基团的桥配体连接的多核半金属茂络合化合物及其制备方法,及使用本化合物为催化剂的苯乙烯聚合体的制备工艺。

Reaction of 9-bromofluorenewith diethyl malonate and sodium carbonate gives diethyl 2-(9-Fluorenyl)malonate.Aminolysis of diethyl 2-(9-Fluorenyl)malonate in ethylenediamine and propylene diamine give〓 and 〓, respectively.〓 and 〓 were synthesized by the reaction of 9-bromofluorene with oxalyl bisethylenediamine. Copper and nickel complexes of 〓 and 〓 were obtained by the reaction of 〓 and 〓 with copper and nickel salt, respectively, in aqueoussolution and extrusion of two hydrogen ions from the amide groups.

使9-溴芴与丙二酸二乙酯在无水碳酸钠存在下反应合成出2-(9-芴基)丙二酸二乙酯。2-(9-芴基)丙二酸二乙酯在乙二胺中胺解得到配体〓,2-(9-芴基)丙二酸二乙酯在1,2-丙二胺中胺解得到配体〓,使9-溴芴与草酰二乙二胺作用得到配体〓和〓与相应的金属盐作用分别得到它们的铜、镍配合物。

PPARα ligands suppressed OPN promoter actiity, and an actiator protein-1 consensus site conferred this repression. Oerexpression of c-Fos and c-Jun reersed the inhibitory effect of PPARα ligands on OPN transcription, and, in chromatin immunoprecipitation assays, PPARα ligands inhibited c-Fos and phospho–c-Jun binding to the OPN promoter.

PPARα配体可抑制OPN启动子活性,一个激活蛋白-1的一致序列位点与这种抑制有关。c-Fos和c-Jun的过表达可逆转 PPARα配体对OPN转录的抑制作用,并且在免疫沉淀实验中,PPARα配体可抑制c-Fos及磷酸化c-Jun与OPN启动子的结合。

Complex (2) through the dissociated pyromellitic acid hydrogen bonding between the ligand and the phen ligand stacking interaction between the formation of a 3D supramolecular structure, but the complex (3) is only through the phen ligand between the stacking structure of the formation of 3D supramolecular structure.

配合物(2)通过游离的均苯四甲酸配体之间的氢键作用和phen配体之间的,π-π堆积作用形成了3D超分子结构,而配合物(3)则只是通过phen配体之间的π-π堆积作用形成3D超分子结构。

Herein, using grafting strategy we have developed a new kind of sulfamide-amine alcohol ligands by grafting a activator to the traditional aminoalcohols, which led to more rigid tridentate coordination model and benefit to the control of chiral surrounding.

本文提出一种嫁接策略设计新的手性配体,即在传统的氨醇配体上嫁接上一个活化剂就可以得到一类新型的手性磺酰胺-氨醇配体

To design a good lanthanide luminescent sensor, a unique combination of features must be realized: high selectivity and recognition to lanthanide ions; presence of multiple absorbing groups suitable for energy-transfer ; high thermodynamic stability and kinetic internees.

一个优良的发光器件必须具备以下几个条件:配体对金属离子有较高的选择识别性能;配体含有共轭发色团有利于能量从配体向中心离子转移;配合物具有相对较高的动力学和热力学稳定性。

A novel ligand, N, N'-bis (2-hydroxy-1-naphthylidene)-3-oxa-1, 5-diaminopentane , and its Zn , Ni , Co , Cu complex were synthesized. The compositions and structures of the ligand and its complexes were characterized by elemental analyses, MS , IR spectra, DTA-TG and molar conductivity.

合成了含萘酚环Schiff碱开链冠醚配体H〓L〓(N,N'-双-二甘醇二胺)及其过渡金属(Zn、Ni、Co、Cu)配合物,通过元素分析、质谱、红外光谱、摩尔电导对配体及配合物的组成、结构进行了详细的表征,对配体和配合物的溶液和固体荧光性质进行了研究。

Furthermore, the effects of ligands, metal and reaction time on the reaction were also researched, and the process of new ligand-metal catalysis for Diels-Alder reaction was also analyzed according to Evans" square planar mode and Corey"s tetrahedral manner.

我们对影响配体对映选择性能的各种因素,如配体结构、金属离子、反应时间等进行了研究,而且根据Evans的平面四方形模式与Corey的四面体过渡态理论为新配体—金属配合物催化的该反应提出了可能的反应机理,并对产物的优势构型作了理论分析。

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