排序方式: 共有144条查询结果,搜索用时 15 毫秒
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102.
通过使用浓硫酸对2,2′-二羟基-1,1′-二萘的磺化与成环反应得到一种新配体,7-氧杂-二苯芴-3,11-二磺酸。通过水热方法得到了它的两个化合物,[CdL(bipy)2(H2O)][Cd(bipy)2(H2O)2]·L·H2O (1)和[CdL(phen)2(H2O)]·5H2O (2),并通过X-射线单晶衍射分析进行结构表征。化合物1以P1空间群结晶,晶胞参数为a=1.205 5(6),b=1.576 4(8),c=1.954 5(10) nm,α=75.755(9),β=88.093(10),γ=89.035(10)°。化合物2以P21/ c空间群结晶,晶胞参数为a=2.104 0(7),b=1.358 0(4),c=1.428 9(5) nm,β=94.543(6)°。在化合物1中,有两个独立的镉(Ⅱ)离子不对称单元,在其中镉(1)离子和两个联吡啶上的四个氮原子,磺酸配体上的一个氧原子及一个水分子配位;镉(2)离子和两个联吡啶上的四个氮原子和两个水分子配位。两种固体化合物在室温下均显示强的蓝色荧光。 相似文献
103.
A new complex formed from strontium nitrate and 1,8-naphthyridine-N-oxide with a 1:2 stoichiometry has been synthesized and characterized by elemental analyses, infrared spectra, Raman spectra, fluorescence spectra, DTA-TG, solubility and molar conductance measurements. A single crystal X-ray structural analysis indicates that a kind of double bidentate and bridging nitrate group which has never been reported in literature is present in the new complex. The coordination number of the strontium ion is 10. 相似文献
104.
已有的对不同类型双冠醚与碱金属配合物的研究工作表明,双冠醚可与半径比醚穴孔径大的碱金属阳离子发生协同配位作用,形成夹心式结构,熵效应比单冠醚有利,并在配位选择性及配位能力方面均比相应的单冠醚有所增强.然而,关于双冠醚对稀土金属配位行为的研究工作尚不多见.我们已研究了1,8-二羰基亚辛基双(苯并-15-冠-5)与稀土元素的固态配合物,结果表明轻重稀土元素与该双冠醚配体形成双核式和夹心式两种不同的结构,初步说明双冠醚能否对稀土元素发生协同配位作用.除了与金属离子的离子势、冠醚环本身 相似文献
105.
Amide-type tripodal ligands have been used as ac-tive materials in ion-selective electrodes, ion recogni-tion and ion-transfer carrier, etc.,1-3 but their lanthanide complexes have not yet attracted much attention in spite of their high tendency to coordinate towards Ln(III) ions. The first three dimensional network of Eu(III) complex, which contains 1,1,1-tris{[(2-benzylaminoformyl)- phenoxy]methyl}propane (the hexadentate ligand) and Eu(NO3)3 as building block, assembled by coordination … 相似文献
106.
3-乙氧基水杨醛缩N,N-双(3-胺基丙烷)-甲基氨Zn(Ⅱ)配合物的合成、晶体结构及荧光性质 总被引:1,自引:0,他引:1
The reaction of 3-ethoxysalicylaldehyde-N,N-bis (3-aminopropyl)methylamine with Zn (Ⅱ) acetate in CH3CH2OH followed by recrystallization in CH3CH2OH gave rise to colourless block crystals of 3-ethoxysalicylaldehyde-N,N-bis(3-aminopropyl)methylamine Zn(Ⅱ). The compound has been characterized by elemental analysis,IR spectrum, molar conductivity and X-ray diffraction structure determination single crystal. It crystallizes in monoclinic, space group P21/c with a=1.028 91(13) nm, b=1.400 35(12) nm, c=1.733 69(19) nm, V=2.476 6(5) nm3, Z=4, Mr=504.91, Dc= 1.354 g. cm-3, T=298(2) K, F(000)= 1 064,μ(Mo Kα)=0.102 7 cm-1, R =0.068 4 and wR =0.185 3for 2 940 observed reflections with I>2σ(Ⅰ). The fluorescence properties of ligand and the complex also have been investigated. The results show that the fluorescence intensity of the Zn(Ⅱ) complex is very stronger than the ligand. In the crystal, the molecules form 1D chain structure by π-π stacking. CCDC: 675010. 相似文献
107.
A novel podand ligand using crown ether as skeleton and N-benzylsalicylamide as functional arms, 4,5-bi{2′-methylbenzeneaminoformyl)phenoxyl]methyl}-benzo-12-crown-4 (L), and its rare earth nitrate complexes have been synthesized. These complexes were characterized by elemental analysis, conductivity measurements and IR spectroscopy. Spectrographic analyses suggest that the complexes show a similar coordination mode. At the same time, the luminescent properties of the Eu(Ⅲ) and Tb(Ⅲ) complexes were also studied. 相似文献
108.
以稀土硝酸盐和酰胺型半刚性三足桥联配体1,3,5-三[(2’-苄胺甲酰基苯氧基)-甲基】苯(L)为构筑单元组装出一系列具有新颖的(10,3)-a型三维网状配位聚合结构的稀土配合物【REL(NO3)3]n.x射线单晶衍射结果表明,晶体属于正交晶系,P212121手性空间群.配合物中每个配体均以三齿桥联的方式连接在3个稀土离子之间,而每个稀土离子又同时与3个配体的3个羰基氧原子配位,形成一个新颖的无限延伸的(10,3)-a型网状结构.迄今为止,在稀土配合物中这种(10,3)-a型网状配位聚合结构非常少见.室温下,在紫外光激发下Sm(Ⅲ),Eu(Ⅲ),Tb(Ⅲ),Dy(Ⅲ)配合物均表现出中心离子的特征荧光发射. 相似文献
109.
六十年代后,缩二脲(以下简称配体B)与过渡金属等配合物的制备及物性测试已相继报道[1]。但与稀土形成配合物的报道很少,A.Seminara[2]等合成过镨、钕等氯化物与缩二脲的配合物。钪、钇的硝酸盐与缩二脲固体配合物的合成及其性质的研究尚未见报道。我们在无水乙醇介质中合成出ScB4(NO3)3和YB4(NO3)3固体配合物,并研究了它们的差热、红外光谱、摩尔电导及X-射线粉末衍射等性质。 相似文献
110.