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Complex 6 is a tetra-nuclear nickel complex of Schiff base derived from salicylaldehyde and β-amino acid.

本论文中合成和表征了六种-β氨基酸铜西佛碱配合物。

Hydrogeologic unit of sandrock in -708m level is divided three units: one is complex, one is less complex and the other is simple.

本文对-708m水平砂岩水水文地质块段进行了划分，共划分为三个块段：Ⅰ块段复杂、Ⅱ块段较复杂、Ⅲ块段简单。

The results showed that the blending system could form surface gel and internal spumescent char layer to achieve flame retardant properties.The flame retardant properties of flame resistant PA6 contenting TPMP/MA complex system were studied by LOI,UL-94 and cone calorimeter tests.The results showed that the LOI value of PA6/17%MA system was 27.2,and the LOI value of PA6/4%TPMP/13%MA system was 28.6.The UL-94 test was V-0 level.The flame retardant mechanism analysis indicated that the TPMP/MA complex system could form thick intumescent char layer to execute the flame retardant functions both in the condensation phase and the gas phase.

将阻燃剂TPMP、MA复配后添加到PA6中，通过采用LOI、垂直燃烧及锥型量热仪研究了体系的阻燃性能，PA6/17%MA体系的LOI值为27.2，PA6/4%TPMP/13%MA体系的LOI值达到了28.6；上述体系的垂直燃烧性均为V-0级，对阻燃机理的分析表明，TPMP与MA复配应用时，可形成膨胀的较厚炭层，在气相和凝固相共同发挥阻燃作用。

These results demonstrate that the PsbS protein is located within PSll-LHCll supercomplex and lies between PSll reaction center complex and peripheral antenna complex LHCll.

这些结果证明，PsbS位于PSll-LHCll超级复合体中，并且在PSll反应中心复合体和外周天线蛋白复合体LHCll之间。

The binary complex of Al-DNAs then interacts with tetraphenylporphyrin in tetrachloromethane, forming a ternary complex of TPP-Al-DNAs.

该复合物469nm产生强烈增强的BRLS信号，并且I_正比于ctDNA和fsDNA的浓度，可用于灵敏的测定核酸，方法的检出限在皮克级。

NodD binds to and bends target promoters through anchoring two tandem and individual specific DNA sites. NodD functions as a tetramer, which has a V-shaped main body. Tetrameric NodD is to change its own conformation rather than its oligomeric forms in response to small signal molecules. The specific interaction between each NodD DNA-binding domain and each specific DNA site does not alter itself in spite of naringenin induction, and the induced conformational change is transferred from protein to DNA. Only the DNA conformation incited by induced NodD is competent for RNA polymerase to form the transcriptional open complex. It cannot be excluded that NodD may have protein-to-protein contacts with RNA polymerase, and that the NodD conformational change may also directly contribute to the transcriptional open complex formation. However, the NodD conformational change itself cannot serve as the determinant of the transcriptional molecular switch.

通过研究，我们提出了初步的NodD操纵子激活模型：第一，四聚体是NodD蛋白的功能单位，它通过铆钉两个串联的相对独立的DNA靶位点结合被诱导的启动子；第二，小分子配基的结合是改变NodD四聚体的构象而不是引发不同形式的寡聚体，在我们的模型中，NodD四聚体缩小其V形主体的弯折角，进而缩短其DNA结合功能域的间距；第三，小分子信号的诱导并没有改变NodD的DNA结合域和其DNA靶位点的相互作用，NodD的构象改变由蛋白质经其双铆钉位点传递给DNA；第四，只有诱导状态的NodD激发的DNA构象才能有效地使RNA聚合酶形成转录开放复合物；第五，不排除NodD与RNA聚合酶可能有直接的相互接触位点，不排除NodD构象的改变可能直接有利于RNA聚合酶形成转录开放复合物，但是我们认为NodD构象改变本身不是充当转录激活开关的决定因素。

Finally, two tetranuclear Cu~(2+) complexes were constructed from a new salen ligand with alkoxo groups. The two complexes were obtained by the reaction of the same ligand with Cu~(2+) in different solvents, i.e., a stage tetranuclear complex and a pseudo-cubane tetranuclear complex in MeOH and THF, respectively.

最后，本文以Schiff碱类过渡金属配合物发展应用为研究背景，设计并合成了一种新型Schiff碱及其两种构型的Cu金属配合物，发现所设计的具有和三个Schiff碱配体，与Cu_2在不同的反应溶剂中进行配位反应时，可以得到不同结构的配合物。

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。

All the ligands and complexes have been characterized with ~1H-NMR, MS and EA.X-Ray single crystal diffraction reveals that zirconium complex containing the tert-butyl substituted N_2O_2 ligand is an oxo- and hydroxyl-bridged dinuclear structure, which is possibly formed by partial hydrolysis of chlorides at one of the zirconium centers. A tetranuclear zirconium complex has been obtained and chacaterized, which is formed by complete hydrolysis of the chlorides at the zirconium centers.

通过研究配合物的单晶结构，我们发现叔丁基取代的不对称N_2O_2配体与ZrCl_4反应生成的锆配合物为氧桥和羟基桥连接的双核锆配合物，中间过程涉及单核锆配合物中氯原子部分水解，并得到氯原子部分水解的双核锆配合物和全部水(来源：8e6eAB67C论文网www.abclunwen.com)解的四核锆配合物的晶体结构，在晶体培养过程中发现双核锆配合物能够以手性自发拆分结晶析出。

Several novel structures have been determined: Unique ninenuclear complexesincorporating 3d, 4f metals with a sodium ion center, the sodium ion may be serve as atemplate in the formation of these novel complexes; Novel tetranuclear 〓complexes with channels formed by intermolecular weak interactions; First 〓type tetranuclear complex; Peculiar "dimer of dimers" complexes derived frombinuclear complex; Unusual one-dimensional wave chain formed by weakcoordination bonds and hydrogen bonds and two dimensional coordination polymerconstructed through coordination bonds and hydrogen bonds.

1获得了多个文献首报和罕见的特殊结构的配合物：两个同时含有碱金属-过渡-稀土金属的独特的九核配合物；两个具有孔道的稀土-过渡金属异四核配合物；草酰胺类〓四核配合物；两个由双核配合物通过叠氮和单个氯原子连成的四核配合物，尤其是以单个氯桥相连的化合物非常少见；一个由弱配键和氢键连成的具有一维波浪形结构的配合物；一个通过配位键和氢键连成的二维配位聚合物。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。