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All the compounds are characterized by IR and elemental analysis.we design and prepare a bipyridinium supramolecular compound and six coordination compounds, which are also characterized by IR, elemental analysis and X-ray structure analysis. According to X-ray structure analysis, hydrogen bonds and n-n stocking interactions participate in the architecture of three-dimensional framework [H2L1 (NO3)2 (H2O)2]n; one-dimensional zigzag coordination polymer [Hgl21.5CH3OH]n; binuclear metallamacrocycle (HgI2L2)2 3H2O; helical double-stranded one-dimensional coordination polymer [Co2(L2)2-2CH3OH]n; double-stranded one-dimensional coordination polymer [Co2(L3)2-CH3OH-CH3CN]n; and three-dimensional compound [Cu(C5H4NCOO)2(H2O)2]-H2O with hydrogen bonds, three-dimensional coordination polymer {[Cd(C5H6NCOO)2H2O]-DMF}n, which are indirectly obtained from the precursor ligand L3 through metal ion induced the hydrolysis of diamide and self-assembled with the hydrolyzate.

我们首次合成了一个双吡啶鎓超分子化合物和六个过渡金属配合物,并通过IR谱,元素分析和X-ray晶体衍射分析对它们进行了表征。X-ray晶体结构分析表明:超分子化合物[H_2L1·(NO_3)_2·(H_2O)_2]_n是由多种氢键和芳香环间的π-π堆积作用构建的三维无限结构;[HgI_2(L1)·1.5CH_3OH]_n是一维锯齿状配位聚合物;(HgI_2L2)_2·3H_2O是双核金属大环化合物;[Co_2(L2)_2·2CH_3OH]_n是具有一维双螺旋结构的配位聚合物;[Co_2(L3)_2·CH_3OH·CH_3CN]_n为一维双链结构的配位聚合物;以及由非直线形配体L3在金属离子Cu和Cd的诱导作用下发生水解,并且金属离子与水解产物——异烟酸根离子自组装,形成了三维氢键超分子化合物[Cu(C_5H_4NCOO)_2(H_2O)_2]·H_2O和三维配位聚合物{[Cd(C_5H_6NCOO)_2H_2O]·DMF}_n。

The results show that both pure andⅠ-doped complex aresemiconductor, the pure complex, and are insulator.

测定了三种配位聚合物及碘掺杂的配位聚合物的电导率,发现配位聚合物碘掺杂前后都表现为半导体,配位聚合物、和表现为绝缘体。

The coordination mode of La can be described as a distorted aquare antiprism, which was completed by two oxygen atoms from one oxalate, four oxygen atoms from four different PDC ligands, and two oxygen atoms from two water molecules.

La呈现四方反棱柱体的配位模式,分别和2个来自同一个草酸配体的氧原子、4个来自4个PDC配体的氧原子以及2个来自2个配位水分子的氧原子配位

The B and Q bands, the characteristic bands of the two metalloporphyrins, undergo bathochromic shift in some of the Lewis basic solvents. The spectral changes are thought to be due to the axial coordination of these solvents with vanadium in VOTPP and nickel in NiTPP. After axia...

结果表明,金属卟啉可以和一些Lewis碱性溶剂发生轴向配位作用,其特征紫外可见吸收峰发生红移;轴向配位作用与卟啉中心金属离子的外层d轨道电子数、碱性溶剂的供电子能力及其空间构造有关,VOTPP比NiTPP更容易和Lewis碱性溶剂发生轴向配位作用;碱性强、空间阻碍小的Lewis碱性溶剂易于与金属卟啉发生轴向配位作用。

The novel complex (1) in which both benzylic nitrogens and heteroaromatic ones to the same metal ion with the rigid ligand imposed by the large heteroaromatic moiety first time was synthesized; a 2: 1 (ligand: metal ions) type complex which has steric resistance and strong thermochemical driving force was obtained. The crystal structures of characteristic ligand (LA4) and complexes (4, 7, 10), in which one cell includes two moieties: there exist minute difference in coordinated bonds and angles despite the same metal ions with the same ligand, were obtained. It shows that several stable conformation in one complex cell.

首次合成了含邻菲罗啉的具有较大刚性的四氮配体中四个氮原子全部与同一金属离子配位的配合物的晶体结构;得到了一个在空间上存在位阻作用的配体与金属离子2:1结构的晶体;解析了具有特色的一个配体(LA4)和三个配合物(4、7和10)的晶体结构,其中的配体与金属离子的配位作用显示出细微的差异,表明在同一金属配合物的晶胞中,可以同时存在着多个稳定的构象。

The result is that both tin atoms are five-coordination, have a distorted trigonal bipyramidal geometry with an additional week interaction between another oxygen atom and tin atom.

分子中四个羧酸酯基有桥联双齿和单齿两种不同的配位模式;在内环锡和外环锡的配位单元中,锡均形成具有五配位的畸变三角双锥配位构型,同时另有一氧原子与中心锡原子之间有弱相互作用。

In complexes 8~16 synthesized by hydrothermal method, most of the ligands adopt multidentate coordination modes joining several lanthanide ions into high-dimensional coordination polymers. And changing of 5-substituting group on isophthalic acid has a little effect on the coordinated abilities of the meta-carboxyl groups.

水热法制备的配合物8~16中,配体多采取多齿配位模式桥连多个稀土离子,形成高维配位聚合物,同时由于羧基氧原子和稀土离子的强的键合力,间苯二甲酸的5位取代基的变化对间位羧基的配位能力的影响不大。

In the thesis, a series of novel single and multi-armed oxadiazole bridging ligands and pyridyl-4, 5-imidazole dicarboxylic acid ligands have been synthesized. The coordination chemistry of these novel ligands with transition metal ions was investigated. In addition, two 1, 3, 4-oxadiazole bridging ligands end-capped by chelating Schiff-base coordination sites have been designed and synthesized. The coordination chemistry based on one of the two ligands with metal ions was primarily investigated.

本文报道了一系列新颖的含1, 3, 4-Oxadiazole杂环的单臂及多臂有机配体,研究了它们与过渡金属离子的配位反应化学;合成了吡啶基-4,5-咪唑二羧酸有机配体,研究了它们在水热条件下与过渡金属离子的配位反应化学;另外,还合成了1, 3, 4-Oxadiazloe杂环桥联的双Schiff-base有机配体,初步探讨了其与过渡金属离子的配位反应化学。

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。

L acted as tridentate ligand to chelate with metal atom in enol and ketone form respectively; In complex anion Co atom reside in tetrahedral coordination environment.

钴原子位于八面体配位环境中,配体L分别以烯醇式和酮式充当三齿配体与金属原子配位,配阴离子中Co原子位于四面体配位环境中。

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