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1.
A novel Mn coordination polymers, Mn2(ADB)2(DMSO)4·DMSO (H2ADB=4,4′-azodibenzoic acid), has been prepared by solvothermal reaction and characterized by element analysis, IR spectra and single-crystal X-ray diffraction. The crystallographic data shows that the title complex crystallizes in monoclinic space group C2/c. Each Mn(Ⅱ) is six-coordinated to four O atoms from three ADB2- ligands, two oxygen atoms from two DMSO molecule and forms distorted octahedral coordination geometry. The Mn(Ⅱ) dimers by the carboxyl groups of the ADB2- ligands were interlinked together by the different carboxylate coordination modes of ADB2- ligands, to yield scaffolds with 2D network with 4.82 topological structures. CCDC: 745678. 相似文献
2.
噻吩甲酰基吡唑啉酮缩氨基酸稀土配合物的合成、表征及生物活性 总被引:7,自引:0,他引:7
A new amino-acid Schiff base, 1-phenyl-3-methyl-4-(2-thenoyl) pyrazolone-5-β-alanine (HL) and its ten rare earth complexes have been synthesized. On the basis of elemental analysis and molar conductance, the general formula of the complexes, [REL2NO3]·nH2O (RE=La, Nd, Eu, Tb, Y, n=2; RE= Pr, Sm, n=1; RE= Dy, Er, Yb, n=3), is given. They were characterized by IR, UV-visible, 1H NMR, 13C NMR and fluorescence. The results show that the rare earth ions exhibit coordination of eight in the complexes.The antibacterial experiments indicate that they have high antibacterial activities against S. Aureus, B. Subtillis, E. Coli, E. Carotovora and C. Flaccumfaciens. 相似文献
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A new dinuclear complex [Tb2(BA)6(2,2′-bipy)2] (BA=4-(trifluoromethyl)benzoic acid, 2,2′-bipy=2,2′-bipyridine) has been synthesized. The complex was characterized by X-ray single-crystal structure analysis. The complex is a dimer with an inversion center. In the complex, two Tb3+ ions are linked by four carboxylate groups of BA ligands in bridging-bidentate coordination mode. Each Tb3+ ion is eight-coordinated with two nitrogen atoms from one 2,2′-bipy molecule, four oxygen atoms from four bridging-bidentate BA ligands and two oxygen atoms from one chelating-bidentate BA ligand. Intermolecular hydrogen bonds are formed in the crystal. The complex exhibits strong green fluorescence under ultraviolet light and the fluorescence spectrum consists of four lines peaking at 489, 545, 584 and 620 nm, which are corresponding to the 5D4→7Fj (j=6~3) transitions of Tb3+ ion, respectively. CCDC: 727763. 相似文献
4.
A new mononuclear gadolinium complex [Gd(NO3)·L](NO3)2 of Schiff base cryptand was obtained by condensation of tris (2-aminoethyl)amine with 2,6-diformyl phenol in template procedure. The complex was characterized by elemental analysis, IR, and x-ray single crystal diffraction analysis. Gadolinium is nine-coordinate in trigonal tricapped prism with five oxygen atoms from three phenols and a bidentate nitrate group, and four nitrogen atoms from three imino C=N bonds and a tertiary amine in the cryptand. The complex crystallized in triclinic system space group P1, a=1.0839(2) nm, b=1.2600(4) nm, c=1.7595(4) nm, α=82.09(2)°, β=89.22(2)°, γ=84.06(2)°, V=2.367(2) nm3, Z=2. 相似文献
5.
Six palladium(Ⅱ) complexes with isonitrosoethylacetoacetate imine Schiff base ligands, Pd(R-IEAI)2, were prepared and characterized by IR, Raman and electronic spectra. Complex tran Pd(p-CH3C6H4-IEAI)2 (2) cry- stallizes in the monoclinic system, space group P21/c,with a=1.2002(2),b=0.9972(2),c=1.1121(2)nm,β=90.43(3)°,Z=2,F(000)=616,μ=7.44cm-1. The final R and wR are 0.0244 and 0.0625 for 2620 ob-served reflections with I≥2σ(I), respectively. The geometry around the Pd(Ⅱ) ions in those complexes has a distorted PdN4 square plane, the Schiff base ligands R-IEAI- being coordinated through their oximino-nitrogen atoms and imino-nitrogen atoms. 相似文献
6.
Four ternary solid complexes were synthesized with sodium diethyldithiocarbamate (NaEt2dtc)(b), 1,10-phenanthroline (o-phen) (c) and hydrated lanthanide chlorides in absolute ethanol by an improved reported method. The complexes were identified as the general formula of RE(Et2dtc)3(phen) (RE=La, Pr, Nd, Sm) by chemical and elemental analyses. IR spectra of the complexes showed that the RE3+ was coordinated with sulfur atoms of NaEt2dtc and nitrogen atoms of o-phen. The constant-volume combustion energies of complexes, ΔcU, were determined by a precise rotating-bomb calorimeter at 298.15 K. The standard enthalpies of combustion, ΔcHm?, and standard enthalpies of formation, ΔfHm?, were calculated for these complexes, respectively. 相似文献
7.
A hydrated tetra-carboxylato-bridged dinuclear copper(Ⅱ) complex [Cu2(mEP)2(H2O)2]2 (1) (mEp is mono -ethyl phthalate or 1,2-benzenedicarboxylate monoethyl ester) has been prepared and characterized by X-ray diffraction single crystal structure analysis and magnetic measurements. This dinuclear complex adopts dimeric paddle-wheel cage structure and the coordination model around each copper(Ⅱ) atom is square-pyramidal with four oxygen atoms of the carboxylate groups from four different mono-ethyl phthalate ligands and one oxygen atom of water as apical position. The magnetic data for 1 exhibited strong intramolecular antiferromagnetic interaction between the two paramagnetic metal ions with 2J=-315.18 cm-1. Comparing with other related complexes in structure and magnetic propertity, the main factor which determines the strong antiferromagnetic interaction in the dimeric copper(Ⅱ) carboxylates is the electronic structure of the bridging O-C-O moiety. CCDC: 624561. 相似文献
8.
Cu(Ⅱ)-牛磺酸缩水杨醛席夫碱配合物的合成及晶体结构 总被引:21,自引:1,他引:21
The title complex was synthesized by reaction of taurine salicylic schiff base(TSSB), O-phenanthroline(phen) and cupric acetate in water-ethanol solution. The crystal structure was determined by X-ray diffraction method and the chemical formula weight of the complex is 498.00. And the crystal structure belongs to orthorhombic system with space group Pbcn and cell parameters: a=31.072(4)?, b=12.8909(18)?, c=10.3478(14)?; V=4144.7(10)?3,Z=8,Dc=1.596Mg·m-3,μ=1.197mm-1 and F(000)=2048. The compound is an one-dimensional chain complex of infinite length connecting with hydrogen bonds. The Cu(Ⅱ) was coordinated by two oxygen atoms and three nitrogen while the O atoms of Ac- groups did not coordinate. At the same time the Cu(Ⅱ)formed a distorted tragonal cone. Besides the capacities of coordination to Cu(Ⅱ) of atoms were discussed. 相似文献
9.
5-Chloro-2-methoxybenzoates of heavy lanthanides and yttrium were obtained as di- or tetrahydrates with a metal to ligand
ratio of 1:3 and general formula: Ln(C8H6ClO3)3⋅nH2O, where n=2 for Ln=Tb, Dy, Y and n=4 for Ln=Ho, Er, Tm, Yb, Lu. The complexes were characterized by elemental analysis, IR and FIR spectra,
thermogravimetric studies, X-ray diffraction and magnetic measurements. The carboxylate group appears to be a symmetrical,
bidentate, chelating ligand. All complexes are polycrystalline compounds. Their thermal stabilities were determined in air
and in nitrogen atmospheres. When heated they dehydrate to form anhydrous salts which next in air are decomposed to the oxides
of the respective metals while in nitrogen to the mixtures of carbon and oxides or carbon and oxychlorides of respective metals.
The complexes are more stable in air than in nitrogen.
The solubilities of yttrium and heavy lanthanide 5-chloro-2-methoxybenzoates in water at 293 K are of the order of 10–3 mol dm–3
The magnetic moments of the complexes were determined over the range 77–298 K. They obey the Curie–Weiss law. The values of
μeff calculated for all compounds are close to those obtained for Ln3+ by Hund and Van Vleck. The results indicate that there is no influence of the ligand field of 4f electrons on lanthanide
ions and the metal ligand bonding is mainly electrostatic in nature.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
10.
新型双核席夫碱配合物的合成及谱学性质 总被引:1,自引:0,他引:1
Eight novel binuclear tetradentate Schiff base complexes (M=Cu(Ⅱ),Ni(Ⅱ),Zn(Ⅱ)) are synthesized. The structure of complexes is two discrete Schiff base unit bridged. The complexes were condensed from series sub-stituent Ketones (5-chloro-2-hydroxybenzophenone, 5-methyl-2-hydroxy-benzophenone, 5-Bromo-2-hydroxybenzop- henone) and dialdehydes (5,5′-methylene-disalicylaldehyde) with the amino group of 1,2-diaminobenzene, and by Metal ion as template. The compounds were characterized by elemental analyses, FT-infrared spectra, Raman, 1H NMR, UV-vis electronic spectra, EPR spectra. The FT-infrared spectra and Raman spectra of complexes were compared and discussed. The UV-vis election spectra, 1H NMR and EPR spectra of complexes have also been attributed and minutely analyzed. 相似文献
11.
Taha ZA Ajlouni AM Al-Hassan KA Hijazi AK Faiq AB 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,81(1):317-323
Eight new lanthanide metal complexes [LnL(NO(3))(2)]NO(3) {Ln(III) = Nd, Dy, Sm, Pr, Gd, Tb, La and Er, L = bis-(salicyladehyde)-1,3-propylenediimine Schiff base ligand} were prepared. These complexes were characterized by elemental analysis, thermogravimetric analysis (TGA), molar conductivity measurements and spectral studies ((1)H NMR, FT-IR, UV-vis, and luminescence). The Schiff base ligand coordinates to Ln(III) ion in a tetra-dentate manner through the phenolic oxygen and azomethine nitrogen atoms. The coordination number of eight is achieved by involving two bi-dentate nitrate groups in the coordination sphere. Sm, Tb and Dy complexes exhibit the characteristic luminescence emissions of the central metal ions attributed to efficient energy transfer from the ligand to the metal center. Most of the complexes exhibit antibacterial activity against a number of pathogenic bacteria. 相似文献
12.
合成了双水杨醛缩1,10-癸二胺Sch iff碱配体(C24H32N2O2,以L表示)与稀土Ln3+的15种新的固体配合物[LnL(NO3)3].nH2O(Ln=La,Ce,Pr,Nd,Sm,Eu,n=0;Ln=Gd,Tb,Dy,Ho,Er,Tm,Yb,Lu,Y,n=1).利用元素分析、摩尔电导、红外光谱、热分析等方法进行表征.中心金属离子Ln3+与Sch iff碱配体中的酚羟基氧以及硝酸根中的氧发生配位,配位数为8. 相似文献
13.
由邻香兰素缩邻氨基苯甲酸(以H2L表示)与稀土硝酸盐作用合成了3种新的固体配合物。对这些配合物进行了元素分析、红外光谱、紫外光谱、差热-热重及摩尔电导分析,确定配合物的组成为[Ln(HL)(NO3)(H2O)]NO3(Ln=Tb,Ho,Lu)。推测了配合物的配位方式和结构 相似文献
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合成并表征了直链醚席夫碱双水杨醛缩二甘醇二胺与Ln^3+和Zn2+的8种异双核配合物「LnZn(SALDA02(NO3)3」(NO3)2.2H2O(Ln=Pr,Sm,Gd,Tb,Er,Yb,Y)。以IR,UV光谱,特别是^1H及^13 CNMR谱等方法研究并讨论了配合物的合成方法,组成,结构及配位方式。 相似文献
17.
邻香草醛缩丙氨酸盐及邻菲咯啉与Ln(Ⅲ)三元配合物的合成与表征 总被引:3,自引:1,他引:2
某些水扬醛类氨基酸的金属配合物具有特殊的性质和应用[1 ,2 ] ,近年来 ,过渡金属离子的此类希夫碱配合物有不少报道。本工作在无水乙醇体系中 ,用稀土硝酸盐与邻香草醛缩丙氨酸钾及邻菲咯啉作用合成了未见文献报道的三种混配配合物 ,并对其组成和配位方式进行了研究。1 实验部分1 1 主要仪器与试剂美国Bio RadFIS1 65型红外光谱仪 ,KBr压片 ;美国PE2 4 0 0 (Ⅱ )型元素分析仪 ;岛津UV 30 0 0双光束分光光度计 ;DDS 1 1A型电导率仪 ;德国STA40 9ZP热分析仪。Ln2 O3纯度高于 99 9% ;DL α 丙氨酸为生化试剂… 相似文献
18.
稀土与邻香兰素二胺类双Schiff碱配合物合成及其性质的研究 总被引:6,自引:0,他引:6
在非水体系中首次合成了硝酸稀土(III)的邻香兰素(2-羟基-3-甲氧基苯甲醛)与乙二胺(L^1)、联苯胺(L^2)、邻苯二胺(L^3)和间苯二胺(L^4)的双Schiff碱配合物(1-8)。通过测定红外光谱、摩尔电导、X射线衍射和X射线光电子能谱推断了配合物的结构和键合情况,配合物的中心金属离子与配体中的二个氮原子、二个氧原子和二个硝酸根中的四个氧原子配位,其配位数为8。通过热重及差热分析发现配合物在低于230℃时很稳定,对于同一配体与不同中心金属离子形成的配合物来说,其热稳定性随稀土离子半径的减小而降低。在77K时测试了铕配合物的激发光谱和荧光光谱,观察到Eu^3^+的特征发射峰。 相似文献
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The enantiopure amine macrocycle H(3)L, as well as the parent macrocyclic Schiff base H(3)L1, the 3 + 3 condensation product of (1R,2R)-1,2-diaminocyclohexane and 2,6-diformyl-4-methylphenol, are able to form mononuclear complexes with lanthanide(III) ions. The lanthanide(III) complexes of H(3)L have been studied in solution using NMR spectroscopy and electrospray mass spectrometry. The NMR spectra indicate the presence of complexes of low C(1) and C(2) symmetry. The (1)H and (13)C NMR signals of the Lu(III) complex obtained from H(3)L have been assigned on the basis of COSY, TOCSY, NOESY, ROESY and HMQC spectra. The NMR data reveal unsymmetrical binding of lanthanide(III) ion and the presence of a dynamic process corresponding to rotation of Lu(III) within the macrocycle. The [Ln(H(4)L)(NO(3))(2)](NO(3))(2)(Ln = Sm(III), Eu(III), Dy(III), Yb(III) and Lu(III)) complexes of the cationic ligand H(4)L(+) have been isolated in pure form. The X-ray analysis of the [Eu(H(4)L)(NO(3))(2)](NO(3))(2) complex confirms the coordination mode of the macrocycle determined on the basis of NMR results. In this complex the europium(III) ion is bound to three phenolate oxygen atoms and two amine nitrogen atoms of the monoprotonated macrocycle H(4)L(+), as well as to two axial bidendate nitrate anions. In the presence of a base, mononuclear La(III), Ce(III) and Pr(III) complexes of the deprotonated form of the ligand L(3-) can be obtained. When 2 equivalents of Pr(III) are used in this synthesis Na(3)[Pr(2)L(NO(3))(2)(OH)(2)](2)NO(3).5H(2)O is obtained. The NMR, ES MS and an X-ray crystal model of this complex show coordination of two Pr(III) ions by the macrocycle L. The X-ray crystal structure of the free macrocycle H(3)L1 has also been determined. In contrast to macrocyclic amine H(3)L, the Schiff base H(3)L1 adopts a cone-type conformation resembling calixarenes. 相似文献