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1.
Two new mixed-ligands lanthanide coordination polymers, [Ln(Ac)(ip)(H2O)2]·0.5H2O (Ln=La (1); Ln=Eu (2); Ac=acetate; ip=isophthalate) have been synthesized under hydrothermal condition. Single-crystal X-ray analyses show that complexes 1 and 2 are three-dimensional structure in which lanthanide ions are bridged by monocarboxylate ligand, acetate or dicarboxylate ligand, isophthalate. And the central lanthanide ions, La3+ and Eu3+, are both nine-coordinate with oxygen atoms. The thermogravimetric analysis was carried out to examine the thermal stability of the title complexes. And the photoluminescence property of complex 2 was also investigated. 相似文献
2.
Chong-Bo Liu Hui-Liang Wen Sheng-Shui Tan Xiu-Guang Yi 《Journal of Molecular Structure》2008,879(1-3):25-29
Two new lanthanide coordination polymers with mixed-carboxylates, [Ln(OX)(HAPA)(H2O)]n[Ln = Eu (1), Ho (2); H2APA = 5-aminoisophthalic acid; OX = oxalate] were obtained by hydrothermal reactions, and characterized by single crystal X-ray diffraction, elemental analysis and IR spectra. Complexes 1 and 2 are both 3-D supramolecular structure, in which lanthanide ions are bridged by oxalate and 5-aminoisophthalate ligands forming 2-D metal–organic framework, and 2-D networks are further architectured to form 3-D supramolecular structures by hydrogen bonds. The two carboxylate groups of H2APA ligand are all deprotonated and exhibit chelating and bridging bidentate coordination modes, respectively, and the amino group in HAPA presents – in the titled complexes. The thermogravimetric analysis was carried out to examine the thermal stability of the titled complexes. And the photoluminescence property of 1 was investigated. 相似文献
3.
Jing Xu Qing Liu Taka-aki Okamura Man-Sheng Chen Wei-Yin Sun Norikazu Ueyama 《Solid State Sciences》2009,11(11):1903-1907
Reactions of ligand 5-(1H-imidazol-4-yl)methylaminoisophthalic acid (H3L) with varied lanthanide metal salts led to the formation of five scalelike 2D layered complexes {[Ln(H2L)(HL)(H2O)2]·H2O}n [Ln(III) = Pr(III) (1), Nd(III) (2), Sm(III) (3), Gd(III) (4), Tb(III) (5)]. The single crystal X-ray diffraction analyses revealed that five complexes crystallized in the same monoclinic space group C2/c are isomorphous and isostructural, and the 2D networks are further connected by hydrogen bonds and π–π interactions resulting in formation of 3D structures. Investigations on the visible luminescent property of the complexes demonstrate that compounds 3 and 5 show characteristic emissions of Sm(III) and Tb(III) in the solid state at room temperature, respectively. 相似文献
4.
Ying-Fen Ran Martin Steinmann Marc Sigrist Shi-Xia Liu Jürg Hauser Silvio Decurtins 《Comptes Rendus Chimie》2012,15(10):838-844
The explorative lanthanide coordination chemistry of 4′,5′-bis-(propylthio)tetrathiafulvenyl[i]dipyrido[3,2-a:2′,3′-c]phenazine (TTF-dppz) is described. Thereby, four new Ln(III) complexes, [Ln(NO3)3(TTF-dppz)2] with Ln(III) = Nd (1), Eu (2), Gd (3), Tb (4), have been prepared and characterized. An X-ray crystallographic study of [Gd(NO3)3(TTF-dppz)2] (3) shows that the Gd(III) ion is coordinated to six oxygen atoms from three bidentate nitrate ligands and four nitrogen atoms from two bidentate TTF-dppz molecules forming a distorted bicapped square antiprism coordination geometry. The UV-vis spectra of the four Ln(III) complexes show very strong absorption bands in the UV region consistent with ligand centred electronic π-π* transitions and an intense broad absorption band in the visible region corresponding to a spin-allowed electronic π-π* 1ILCT transition from the TTF-dppz ligand. Upon coordination, the 1ILCT band of the free TTF-dppz ligand is bathochromically shifted. The electrochemical studies reveal that all complexes undergo two reversible oxidation and one (quasi)reversible reduction processes, ascribed to the successive oxidations of the TTF moiety and the reduction of the dppz unit, respectively. Moreover, the magnetic properties of complexes 3 and 4 are discussed. 相似文献
5.
《Journal of Coordination Chemistry》2012,65(18):1973-1982
Six new lanthanide Schiff-base complexes were synthesized by reactions of hydrated lanthanide nitrates with H2L (H2L?=?N,N′-bis(salicylidene)-1,2-cyclohexanediamine) and characterized by elemental analysis, DTA–TG, IR, UV and luminescence spectra. The microanalyses and spectroscopic analyses indicate a 1D polymeric structure with the formula of [Ln(H2L)(NO3)3(MeOH)2] n [Ln?=?La (1), Ce (2), Pr (3), Sm (4), Gd (5) & Dy (6)]. The fluorescence spectrum of complex 4 exhibited Sm3+ centered, Schiff-base sensitized orange fluorescence, indicating that energy levels of the triplet state of H2L match closely to the lowest excited state (4G5/2) of Sm3+ ion. 相似文献
6.
《Journal of Coordination Chemistry》2012,65(18):2075-2081
The hydrothermal reactions of Nd(ClO4)3·6H2O, Gd(ClO4)3·6H2O, Dy(ClO4)3·6H2O, Er(ClO4)3·6H2O with 1,3-dicyanobenzene, give rise to four one-dimensional rare earth-based coordination polymers: [M(3-CNC6H4COO)3(H2O)2] n (where M?=?Nd (1), Gd (2), Dy (3), Er (4), 3-CNC6H4COO?=?3-cyanobenzoato), respectively. Their solid-state structures have been characterized by X-ray single-crystal diffraction studies. The results show that 1,3-dicyanobenzene hydrolyzed to give 3-cyanobenzoato under hydrothermal condition, and the four complexes are isomorphous. Crystal data for 1: triclinic, space group P-1, a?=?9.4063(19), b?=?11.485(2), c?=?12.616(3)?Å, α?=?66.38(3), β?=?74.01(3), γ?=?86.96(3)°, V?=?1197.9(4)?Å3, Z?=?1, D c?=?1.704?Mg?m?3; for 2: triclinic, space group P-1, a?=?9.3712(19), b?=?11.446(2), c?=?12.627(3)?Å, α?=?65.86(3), β?=?73.89(3), γ?=?86.84(3)°, V?=?1184.8(4)?Å3, Z?=?1, D c?=?1.759?Mg?m?3; for 3: triclinic, space group P-1, a?=?9.3425(19), b?=?11.432(2), c?=?12.703(3)?Å, α?=?65.28(3), β?=?73.80(3), γ?=?86.86(3)°, V?=?1180.6(4)?Å3, Z?=?1, D c?=?1.780?Mg?m?3; for 4: triclinic, space group P-1, a?=?9.3425(19), b?=?11.432(2), c?=?12.703(3)?Å, α?=?65.28(3), β?=?73.80(3), γ?=?86.86(3)°, V?=?1180.6(4)?Å3, Z?=?1, D c?=?1.7794?Mg?m?3. The fluorescence emission spectra of compounds 1 to 4 are also reported. 相似文献
7.
《Journal of Coordination Chemistry》2012,65(13):2157-2166
Three new lanthanide coordination polymers, [Ln(Ad)3/2(Phen)] n ·2nH2O (Ln = Eu, 1; Pr, 2; Ad = adipate; Phen = 1,10-phenanthroline) and [Yb(Ad)3/2(Phen)] n ·nH2O 3, were prepared by hydrothermal reactions. The structures of 1, 2 and 3 are reported. In compound 1, Eu(III) ions are bridged by adipate ligands in two modes into 2-D polymeric layers. Adjacent layers are assembled by hydrogen bonding and π–π stacking between 1,10-phenanthrolines into a 3-D supramolecular structure. Compound 2 is isostructural with 1. In compound 3, the Yb(III) ions are connected by adipate ligands in three modes into a 3-D network. 相似文献
8.
《Journal of Coordination Chemistry》2012,65(17):2796-2803
Direct reaction of pyridine-3,5-dicarboxylic acid (H2PDA) and oxalic acid (H2ox) with Ln(ClO4)3 · nH2O under hydrothermal conditions gave three 3-D coordination networks, [Ln(PDA)(ox)0.5(H2O)2] · H2O [Ln = La(1), Nd(2), and Eu(3)]. The complexes were characterized by elemental analysis (EA), X-ray single-crystal diffraction, infrared spectroscopy (IR), and thermogravimetric analysis (TGA). Single crystal X-ray diffractions shows that the compounds are isomorphous and have 3-D framework structures, in which pyridine-3,5-dicarboxylates (PDA2?) link lanthanides to give 2-D layers, which are further fabricated into a 3-D network via bis-bidentate oxalate bridging. Luminescence of 3 is investigated. 相似文献
9.
《Journal of Coordination Chemistry》2012,65(19):2097-2105
Hydrothermal reactions of Sm2O3, Gd(ClO4)3?·?6H2O and Tb(ClO4)3?·?6H2O with nitrilotriacetic acid, give rise to three lanthanide coordination polymers, {[Sm(NTA)(H2O)2]?·?H2O} n (1), {[Gd(NTA)(H2O)]?·?H2O} n (2) and {[Tb(NTA)(H2O)]?·?H2O} n (3). Their solid-state structures have been characterized by elemental analysis, and IR spectroscopy. X-ray single-crystal diffraction analyses indicated that 2 and 3 are isomorphous three-dimensional coordination polymers with eight-coordinate Gd(III) (or Tb(III)), while 1 forms a two-dimensional coordination polymer containing nine-coordinate Sm(III). The photophysical properties of 3 have been studied with excitation and emission spectra, which exhibit strong green emission. 相似文献
10.
Zhao-Yang Li Jing-Wei Dai Xiao-Xu Li Ying-Liang Liu 《Journal of Molecular Structure》2010,963(1):50-49
Three novel lanthanide complexes, namely, [Ce(Himdc)(H2imdc)(H2O)3]·H2O (1), {[Dy(Himdc)(Ox)0.5(H2O)2]·H2O}n (2), and {[Nd(Himdc)(Ox)0.5(H2O)2]·H2O}n (3) (H3imdc = imidazole-4,5-dicarboxylic acid, Ox = oxalate), have been successfully prepared by the assembly of lanthanide ions and H3imdc ligand under different synthetic conditions. All of the complexes have been characterized by means of elemental analysis, IR, TG analysis, luminescence spectroscopy as well as single-crystal X-ray diffraction analysis. The 3D supramolecular structure of 1 is constructed from 1D zig-zag chains through the hydrogen bonding interactions. Complex 2 possesses the chair-shaped secondary building units (SBUs) with Dy6(Himdc)4(Ox)2 and meso-helical chains (P + M), resulting in a novel 2D structure based on the linkages of oxalate ligand. Complex 3 also presents 2D layer structure with uninodal 6-connected net topology, but crystallizes in the different space group and owns higher coordination number of the central metal atom than complex 2. The luminescence property of 2 is investigated in the solid state at room temperature. 相似文献
11.
《Journal of Coordination Chemistry》2012,65(12):1361-1370
A meso-substituted unsymmetrical porphyrin liquid crystal, 5-(4-myristyloxy)phenyl-10,15,20-triphenyl porphyrin, and a series of its lanthanide complexes, (lanthanide ions: Gd, Tb, Dy, Ho and Er) with acetylacetone were synthesized and characterized by elemental analyses, molar conductances, UV-Vis, IR and 1H?NMR spectra. A structure is proposed in which the porphyrin is as a tetradentate ligand and acetylacetonate is bidentate to the lanthanide. Luminescence spectra show that quantum yields of the Q band fluorescence are in the region 0.027–0.191. DSC data and an optical textural photo using a polarizing microscope indicates that the compounds have liquid crystalline character. 相似文献
12.
Syntheses,structures, thermal stabilities and bacteriostatic activities of four lanthanide complexes
Four lanthanide complexes, [La2(2,4-DClBA)6(5,5′-DM-2,2′-bipy)2(H2O)2]·2C2H5OH (1) and [Ln(2,4-DClBA)3(5,5′-DM-2,2′-bipy)(C2H5OH)]2 (Ln = Pr(2), Sm(3), Gd(4); 2,4-DClBA = 2,4-dichlorobenzoate; 5,5′-DM-2,2′-bipy = 5,5′-dimethyl-2,2′-bipyridine), were synthesized and characterized via elemental analysis, infrared spectra and thermogravimetric analysis (TG). The crystal structures of 1 and 2–4 are different; Each La3+ is nine-coordinate adopting a distorted mono-capped square antiprism, while the Ln3+ ions of 2–4 are all eight-coordinate with a distorted square antiprismatic molecular geometry. There are subtle changes in the local coordination geometry of the lanthanide–5,5′-DM-2,2′-bipy complexes. Binuclear 1 complexes are stitched together via two kinds of hydrogen bonding interactions (OH?O and CH?O) to form 1-D chains along the y axis, while the units of 2–4 are stitched together via CH?O to form 1-D chains along the x axis. TG analysis revealed thermal decomposition processes and thermal stabilities of the complexes. The bacteriostatic activities of the complexes were evaluated against Candida albicans, Escherichia coli, and Staphylococcus aureus. 相似文献
13.
《Journal of Coordination Chemistry》2012,65(17):2755-2763
We have synthesized four coordination polymers with two different nitrogen containing organic ligands and different lanthanide metal ions, under hydrothermal condition. [{Ln2(bpdc)3(H2O)2}] n (Ln = Dy (1), Sm (2)) (bpdc = 2,2-bipyridine-3,3-dicarboxylic acid) are isostructural, with 2-D supramolecular layer structure composed from 1-D chains. Like 1 and 2, [{Ln(pzda)2(H2O)2} · 4H2O] n (Ln = Dy (3), Nd (4)) (pzda = pyrazine-2,6-dicarboxylic acid) are also isostructural with 1-D chain-like structures. The photoluminescence of 2 is studied. 相似文献
14.
15.
Three lanthanide coordination polymers were prepared by hydrothermal synthesis and characterized by single-crystal X-ray diffraction. [Pr2(mBDC)3(phen)(H2O)]n·0.5nH2O (1) (mBDC=isophthalate, phen=1,10-phenanthroline) exhibits two kinds of metal environments (coordination numbers 7 and 8). In complex 1, mBDC ligands adopt the tetradentate (bridging and bridging) coordination mode and connect Pr ions into an undulating layer, and a 3D supramolecular structure is formed via hydrogen bonds between adjacent layers. [Tb4(mBDC)6(phen)]n (2) has three types of metal environments (coordination numbers 6, 7 and 8) and is composed of a 3D network formed by mBDC linking Tb ions via tetradentate (bridging and bridging) and pentadentate (bridging/chelating and bridging) coordination modes. There are two kinds of small quadrilateral channels along the a-axis. [Er4(mBDC)6(phen)]n (3) is isostructural to complex 2. 相似文献
16.
《Journal of Coordination Chemistry》2012,65(23):4185-4193
Five mixed-ligand coordination polymers, [Ln2(PTCP)2(m-BDC)3] n ?·?nH2O (Ln?=?Pr (1), Sm (2), Eu (3), Tb (4), Dy (5); m-BDC?=?1,3-benzenedicarboxylate; PTCP?=?2-phenyl-1H-1,3,7,8-tetraazacyclopenta[l]phenanthrene), were synthesized and characterized by IR spectra, elemental analyses, thermogravimetric analyses, single-crystal X-ray diffraction, and solid-state photoluminescent spectra. X-ray crystallographic analyses reveal that the five complexes are 1-D structures based on dinuclear [Ln2O12N4] units and further assembled into 3-D supramolecular networks by hydrogen bonds and π···π stacking interactions. The solids possess high thermal stabilities, with 3 and 4 exhibiting strong pure red and green characteristic emissions of Eu(III) and Tb(III) at room temperature. 相似文献
17.
William L. Boncher 《Journal of solid state chemistry》2010,183(1):52-56
Polycrystalline lanthanide sulfide materials were formed at low temperatures using a single-source precursor based on the lanthanide dithiocarbamate complex. The synthesis temperatures are generally lower than standard solid state preparations, avoid toxic sulfurizing gases and provide a convenient route to prepare lanthanide chalcogenide nanoparticles. Depending on the reaction conditions and oxophilicity of the lanthanide, the sulfide material was formed with oxidized products including oxysulfides, oxysulfates and the oxide. 相似文献
18.
Trivalent lanthanide complexes of the type K[ML
2] whereM=La(III), Pr(III), Nd(III), Sm(III), Eu(III), Gd(III) and Dy(III) and H2
L=N-isonicotinamidosalicyladimine, have been prepared and characterised. The nephelauxetic ratio (β), covalency (δ) and bonding
parameter (b
2) of K[NdL
2] have been calculated. Infrared spectral studies reveal that N-isonicotinamidosalicylaldimine acts as a dibasic tridentate
ligand. A coordination number six has been proposed for the lanthanide metal ions. 相似文献
19.
《Journal of Coordination Chemistry》2012,65(14):2207-2215
Two aryl amide ligands, N-(p-tolyl)-2-(quinolin-8-yloxy)acetamide (L1 ) and N-(4-chlorophenyl)-2-(quinolin-8-yloxy)acetamide (L2 ), were synthesized. With these ligands, two series of lanthanide(III) complexes were prepared, Ln(L n )2(NO3)3 (n = 1, 2; Ln = La, Sm, Eu, Gd, Dy), and characterized by the elemental analyses, molar conductivity, 1H NMR spectra, IR spectra and TG-DTA. The fluorescence properties of the complexes and the triplet state energies of the ligands were studied in detail. In addition, the quantum yields of both Eu(III) complexes and Eu(L0)2(NO3)3 [where L0 is N-(phenyl)-2-(quinolin-8-yloxy)acetamide] 1 were calculated. The results indicate that among the lowest triplet energies (T) of the three ligands, that of L2 is most suitable to the resonance level (5D1) of Eu(III) ion. Furthermore, Eu(L2)2(NO3)3 has the highest fluorescence intensity and quantum yield of the three Eu(III) complexes. 相似文献
20.
Two lanthanide luminescent coordination compounds based on 3,5-pyrazoledicarboxylate and oxalic acid
《Journal of Coordination Chemistry》2012,65(5):785-793
Two isostructural 3-D complexes [Ln(pdc)(ox)0.5(H2O)2]?H2O (Ln = Tb(1), Eu(2); pdc = 3,5-pyrazoledicarboxylate; ox = oxalate) have been synthesized under hydrothermal conditions. Both are characterized by single crystal X-ray diffraction, elemental analysis, and IR. Compounds 1 and 2 possess a 3-D framework with 1-D rectangular channels built from 2-D, brick-like networks, and pdc ligands. The photoluminescence and lifetimes of 1 and 2 in the solid state have been studied. 相似文献