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trinuclear相关的网络例句

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与 trinuclear 相关的网络例句 [注:此内容来源于网络,仅供参考]

The method of self-consistent field of the intermediate neglect of differential overlaphas been used in the calculations of the binuclear cluster, trinuclear unit of hexanuclear clusterand octanuclear clusters. The results are described as follows: The high-lying MO's of thetrinunclear and binuclear cluster are mostly composed of d-orbitals of the metal cores, and areconsidered as M-M bonding orbitals.

应用INDO/S方法对二核簇合物、六核簇合物中的三核片断和八核簇合物进行了计算,结果表明,二核簇合物与三核簇合物的前线占有轨道主要是由金属簇芯的d轨道组成,是M-M成键轨道。

Mn-complexes in which Mn atom ligand with the N atom within ligand can stimulate the recovery of electron transfer and oxygen evolution. The trinuclear Mn-complex is extremely sensitive to the addition of CaCl2. It is suggested that there is an interaction between Ca2 and carboxyl within the trinuclear Mn-complex during photoactivation and this interaction benefits the ligation of Mn atom to the apo-WOC and form an active WOC. Binuclear MnMn complex shows slightly higher efficiency than binuclear MnMn complex in restoration of O2 evolution activity. It is suggested from our results that recovery of electron transport and O2 evolution with synthetic Mn-complexes is affected by different factors. Cl- can stimulate the reconstitution of WOC at the concentration of over 100mM;the maximal recovery of O2 evolution activity requires the presence of CaCl2 and 33 kDa protein polypeptide together. Bicarbonate can stimulate the reconstitution of WOC.

锰配合物中锰原子与配体中的氮原子配位连接时,能显著恢复电子传递活性和放氧活性;三核锰化合物在重组时对CaCl2的存在非常敏感,我们认为Ca2 与三核锰化合物中的羧基之间存在一定的相互作用,而这种作用有助于锰原子的光配位进而使三核锰化合物易于组装成有活性的水氧化复合物:双核锰化合物MnMn比双核锰化合物MnMn在恢复放氧活性方面更有效;影响锰化合物电子传递能力恢复的因素与影响锰化合物放氧活性恢复的因素不同;在锰蔟重组过程中,氯离子的浓度必须在100mM以上,才能有效进行光重组;最大光重组效率的获得必须有钙离子和33kDa多肽同时存在;碳酸氢根离子促进锰化合物与去锰光系统II的光组装。

The electrode based on trinuclear copper compound has been applied to the determination of thiocyanate in wastewater with satisfactory results.

目前已有以钴卟啉或维生素B12衍生物为载体的硫氰酸根电极[1-2]的报道,本实验室也研究了以席夫碱金属配合

In the structures of these complexes, zinc can act as the vertex of the networks in various styles: single atom; dicarboxylate, tricarboxylate or tetracarboxylate bridged binuclear SBU ; and octacarboxylate bridged trinuclear SBU.

在这些配合物的结构中,锌离子可以按多种形式作为网络结构的顶点:单原子,双羧基、三羧基或四羧基桥连的双核锌次级结构单元,八羧基桥连的三核锌次级结构单元,再与配体组装成不同的配位聚合物网络。

This experiment demonstrated that the trinuclear compound is an excellent precursor for NiFe〓O〓 nanoparticle.Ⅲ.

实验显示这种三核化合物〓是一种很好的制备NiFe〓O〓纳米颗粒的前提物。Ⅲ。

We have studiedthe coordination water-substituted reactions and the phase-transferchemistry of dozens of trinuclear or tetranuclear sandwich-typePOMs and found that organic molecules or polymers can becoordinated to these polyanions after dehydration, thus more thanone hundred coordinated products are obtained, indicating that thesepolyanions are excellent ligands in organic solvents.

我们首次对夹心三、四核等几十种化合物中配位水进行了配位水取代反应及相转移化学研究,脱水后可配位有机分子或有机高分子,得到上百种配位产物,因此在有机溶剂中它们是优秀的配体。

In order to get the information of interaction between metal complex and DNA and select metal complexes which can cleave DNA effectively, twenty seven transition metal complexes containing O/N coordinate atoms have been synthesized in this thesis. We report the synthesis, crystal structure and properties of the complexes. One of the complexes is the first μ〓-oxalato tetranuclear Cu complex, in which there is ferromagnetic interaction between the copper atoms bridged by oxalate ions. Two trinuclear copper complexes containing partial cubane Cu〓O〓 cores have been synthesized and discussed the magnetic properties.

为了解金属配合物与DNA的相互作用及筛选能有效切割DNA的金属配合物,为无机药物合成及应用提供基础信息,本文利用十个含N、O原子的多齿配体设计合成了二十七个未见文献报道的过渡金属配合物,并解析了它们的晶体结构:其中包括首例μ〓-草酸根的四核铜配合物;合成了两个具有μ〓-OH〓三核缺角立方烷结构的Cu配合物;以HCBP衍生物为配体合成了七个过渡金属配合物;以SCN〓、N〓,C〓O〓等为桥联配体,以dmpyen为端基配体合成了十一个配合物。

By modifying the synthetic methods in literature,four multinuclear copper complexes,that is,dinuclear[Cu_2(H_2tea)_2(C_6H_5COO)_2]·2H_2O, trinuclear[Cu_3(H_2tea)_2(4-OC_6H_4COO)_2(H_2O)]·4H_2O(designated as Cu_2),tetranuclear O?

通过改进合成方法,从硝酸铜原料和三乙醇胺(标记为H_3tea)配体出发,合成了四种多核铜配合物,即双核铜配合物[Cu_2(H_2tea)_2(C_6H_5COO)_2]·2H_2O,三核铜配合物[Cu_3(H_2tea)_2(4-OC_6H_4COO)_2(H_2O)]·4H_2O(标记为Cu2),四核铜配合物O?

Compound 20 has a two-dimensional hybrid structure on the basis of A-type Anderson polyoxometalates and trinuclear silver coordination complex subunits and sodium dimmers.

化合物20是将A型Anderson多酸与三核的银配合物簇及钠的二聚体形成的2D杂化结构。

By utilizing three benezenemulticarboxylate derivatives (H2chdc, H2aip, NaH2sip), we obtain 12 coordination polymers. Especially, compelexes 1 and 2 are based on one-dimensional ···OHInOHIn···chains as building units, while complex 3 is based on double four-ring [In8(μ2-O)4(μ2-H2O)8]16+, complex 4 is based on trinuclear In3(μ3-O)(CO2)6, complexes 11 and 12 are both based on nested bistranded helices.

选择了三类取代苯羧酸配体: 2,5-二羟基-1,4-对苯二甲酸(2,5-H2chdc); 5-氨基间苯二甲酸(5-H2aip); 5-磺酸基间苯二甲酸钠盐(5-NaH2sip)和InCl3反应合成了十二个配位化合物:其中1、2以···OHInOHIn···链为构筑单元, 3以双四元环[In8(μ2-O)4(μ2-H2O)8]16+为构筑单元,4以棱柱状三核铟In3(μ3-O)(CO2)6为构筑单元,而11、12以嵌套的双股螺旋链为构筑单元。

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