配体

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。

In addition to the two axial ligations provided by His18 and Met80, the hydrogen bond and hydrophobic interactions between the heme and the protein polypeptide, the heme also covalently linked to the protein matrix through two thioether bonds which are formed between vinyl groups of the heme and cysteine residues of a classic Cys-Xaa-Xaa-Cys-His heme-binding motif of the polypeptide chain.

Cyt c是血红素蛋白中电子传递蛋白的典型代表，其辅基heme与蛋白肽链的结合除了来自heme轴向配体组氨酸(His18)和甲硫氨酸(Met80)的配位作用、氢键和疏水相互作用等非共价键作用方式外，血红辅基heme的两个乙烯基还与蛋白肽链上的结构片段域Cys-Xaa-Xaa-Cys-His中的两个半胱氨酸形成硫醚键以共价键方式相结合。

There is no longer an azido bridge between the two copper atoms, which are 5.123 (4)︿ appart. The macrocycle is in a chair-type conformation.

每个配位多面体由大环穴醚配体提供三个氮原子，叠氮离子提供一个氮原子，两个Cu离子之间不存在叠氮桥，间距为5.12︿。

In the third chapter, eight new complexes of 4, 6-dimethylpyrimidine 2-thioacetic acid with rare earth metals has been synthesized and characterized by means of elemental analysis, molar conductivity, IR,〓 NMR and TG-DTA. The general formula of the complexes is Ln〓(n=4 or 5). In the complexes, the deprotonated ligand coordinated to the rare earth metal ions in chelate bidentate mode. 4 or 5 molecular of crystal water existed in the complexes.

第三章合成了八种4，6-二甲基嘧啶-2-硫代乙酸的稀土配合物，通过元素分析、摩尔电导、红外光谱、核磁共振氢谱和热重-差热对配合物进行了表征，研究结果表明，配合物的组成为Ln〓n=4或5），在配合物中配体羧基脱去质子后采用螯合双齿的方式与稀土离子形成配位键，同时，配合物中含有4或5个结晶水。

In order to investigate therelationship between macrocyclic ligands and rare earth ions, wehave synthesized two new Schiff-base crown ether, two newdiaza-crown ether ligands and their rare earth complexes in thisdissertation. These complexes have been characterized byelemental analyses, IR spectra,〓 NMR spectra, thermalanalyses and molar conductivity measurement, we investigatedtheir ability to form coordination compounds and theircompositions and properties.

为了进一步研究和探讨冠醚配体对稀土元素的配位作用，论文首次报道了两个新希夫碱冠醚、两个新双氮杂冠醚及它们的稀土配合物的合成，并通过元素分析、热分析、核磁共振氢谱、红外光谱及摩尔电导测定，研究了配合物的组成及性质。

Objective: Purpose to investigate the different in vitro function of targetable non-viral vector containing poly-L-lysine or protamine.

DNA-多聚阳离子-配体形成的复合体可以通过受体介导的内吞作用将目的基因靶向性导入含相应配体的细胞中［1］。

In thisthesis our endeavor has been focused on the design of fluoresent sensors for sensinggroup 11 metal ions and phosphines －a very impotant type of organic molecule inthe industral and academic aspects.

三价磷的有机化合物由于其独特的配位能力已经吸引越来越多的人对它们进行深入研究，我们将三价磷受体单元同蒽荧光团有机地结合起来设计合成出下列新型含蒽荧光团双膦配体。

In addition, the relationship between the structure and the third-order nonlinear properties of this complex is discussed.

探讨了配合物的结构和其三阶非线性光学性质的关系，认为配位化合物的丌共轭离域体系的增大和金属中心离子与配体之间的电子转移是配合物具有更大非线性折射率的主要原因。

Two coordination polymers [Pb6(H2O)24]·3H2O(1)(H3cit=citric acid)and Pb(H2O)2(2)(tar=tartaric acid)were synthesized under hydrothermal conditions and characterized via IR,TG-DTA,C,H,N elemental analysis,XRD and single crystal X-ray diffraction analysis.

在水热条件下，合成了2个含柔性配体柠檬酸和酒石酸的二价铅配位聚合物[Pb6(H2O)24]。3H2O(1)(H3cit=citricacid)及Pb(H2O)2(2)(tar=tartaricacid)。用红外光谱、差热-热重、元素分析、粉末X射线衍射及单晶X射线衍射等手段对化合物进行了表征。化合物1属三斜晶系，P1空间群，a=0.97053(19)nm，b=0.9764(2)nm，c=1.0955(2)nm，α=109.016(3)°，β=98.380(3)°，γ=92.136(3)°，V=0.9671(3)nm3，Z=2，R1=0.0420，wR2=0.1049，GOF=1.064。

The regularities of the substitution effects of the electron-pushing group and the electron- withdrawing group on the electronic structures and the related properties of the complexes, e.g. the energies and the compositions of some frontier molecular orbitals, the spectroscopy properties, the atomic net charge populations on main ligands, the coordination-bond lengths and the coordination-bond angles of the complexes, etc. have been investigated.

探讨供电子基团和拉电子基团在主配体上的取代对配合物的电子结构及相关性质，如配合物前沿分子轨道的能量、组成、光谱性质、原子的净电荷布居及配位键长键角等的影响规律。

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。