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1.
1 INTRODUCTION The design and synthesis of metal-organic coor- dination polymers are of current interest owing to their intriguing architectures and potential applica- tions, such as catalysis, fluorescence and magne- tism[1~4]. Many transition metal-organic polymers have been synthesized and exhibit interesting magneticproperties[5~9]. Among them, coordination polymers constructed by dicarboxylate ligands have attracted considerable attention due to their rich coordination modes and di…  相似文献   

2.
1 INTRODUCTION The metal-containing supramolecular frame- works can be constructed through coordinate cova- lent or supramolecular contacts such as hydrogen- bond and π-π stacking[1 ~ 3]. Extended networks possessing higher dimensionalities can be obtained by assembly of coordination polymers (or comple- xes) with lower dimensionalities via hydrogen bond interactions[4~13]. However, normally the higher di- mensional networks are generated by one-dimen- sional chains through hydrogenbo…  相似文献   

3.
1 INTRODUCTION In recent years, coordination polymeric frame- works have attracted great attention not only due to their potential applications in the areas of magnetism, nonlinear optics, electronics, catalysis, and molecu- lar recognition and sorption but also to their intri- guing structure topologies[1~8]. The coordination polymers can be specially designed by careful selec- tion of the metal ions with definite coordination geometry, the structure of the connecting ligands, the nature…  相似文献   

4.
1 INTRODUCTION The synthesis of organic-inorganic hybrid open framework materials based on transition metals has become widespread over the past decade[1~3]. In contrast to transition-metal complexes, lanthanide complexes are much less studied. Owing to large radii, high coordination numbers, special fluore- scence and magnetic properties of lanthanides, lan- thanide coordination polymers have attracted con- siderable interest[4]. Different ligands, such as the N- and O-donor ligands, h…  相似文献   

5.
1 INTRODUCTION Coordination polymers have attracted the atten- tion of chemists, physicists, and materials scientists owing to their fascinating structures and potential functional applications in the last decade[1~4]. The bridging ligands play a central role in constructing functional coordination polymers, and weak nonco- valent interactions like hydrogen bonding or π-π stacking plays an important role in molecular self- assembly[5~7]. As a multidentate and rigid ligand with multi-pr…  相似文献   

6.
1 INTRODUCTION Recently, much attention has been focused on metal- organic coordination polymers for their structural novelty and potentially important applications as advanced materials[1~3]. With the development of crystal engineering and supramolecular chemistry, it is possible to use organic ligands and metal salts to construct metal-organic coordination polymers pos- sessing some specific properties. Furthermore, inve- stigations on coordination complexes containing rare earth ion ha…  相似文献   

7.
1 INTRODUCTION The metal-organic coordination polymers have proved to be promising in developing new mate- rials[1]. It is crucial to select or synthesize the suita- ble bridging organic ligand. Some simple rigid li- gands are skillfully employed[2~4].…  相似文献   

8.
Synthesis and Crystal Structure of [La(BTC)(H2O)6]n   总被引:1,自引:0,他引:1  
1 INTRODUCTION desired topologies owing to their rich coordination modes[8~12] and we have been exploring the chemi- The assembly of metal-organic infinite frame- stry of coordination polymers constructed by tran- works via coordination of metal ions with multifunc- sition metals and benzoic multicarboxylic acids[13~16]. tional organic ligands is a field of increasing inte- In addition, lanthanide ions have high affinity for rest[1~4]. A rational designed and predictable coor- hard donor a…  相似文献   

9.
1 INTRODUCTION The rational design and synthesis of metal-organic coordination polymers have generated considerable interest in supramolecular chemistry and material science owing to their intriguing structural diver- sities and potential applications as functional mate- rials[1~3]. Up to now, some structural motifs with specific topologies and functions have been con- structed through rational combination of organic li- gands containing appropriate coordination sites and metal ions beari…  相似文献   

10.
1 INTRODUCTION The coordination chemistry of Pd(Ⅱ) com- plexes with didentate nitrogen coordination ligands has been extensively studied for a few decades[1]. Pd(Ⅱ) trends to bond to the didentate nitrogen in cis-mode and such complexes have potential usage in the emerging area of self-assembly[2]. We will report herein the synthesis and crystal structure of a cis-coordinated mononuclear Pd(Ⅱ) complex with one 1,10-phenanthroline and two THF as ligands, 1. 2 EXPERIMENTAL 2. …  相似文献   

11.
The title compound [Cd(Hq)2(Hdpa)2] (Hq = 8-hydroxyquinoline, H2dpa = diphenic acid) has been synthesized and characterized by single-crystal X-ray diffraction analysis. It crystallizes in monoclinic, space group C2/c with a = 20.6880(5), b = 14.2584(4), c = 13.4776(4) (A), β = 113.434(2)°, C46H28Cd1N2O10, Mr = 881.10, V = 3647.68(17) (A)3, Z = 4, Dc = 1.604 g/cm3, F(000) = 1784,μ = 0.668 mm-1, the final R = 0.0576 and wR = 0.1157 for 2631 observed reflections with I >2σ(Ⅰ). The centrosymmetric Cd(Ⅱ) ion is six-coordinated in a slightly distorted octahedral geometry.The intermolecular hydrogen bonds extend the mononuclear structure into a one-dimensional supramolecular framework. The fluorescence spectrum of the compound exhibits intense emission at 520 nm when excited at 330 nm in solid state at room temperature.  相似文献   

12.
1 INTRODUCTION The crystal engineering and design of solid-state coordination polymers have become a very attrac- tive field in recent years[1~4]. Many interesting fra- meworks with intriguing potential applications have been obtained through the self-assembly of selected metal centers and carboxylate ligands[5, 6]. Compared with aromatic carboxylate ligands such as terephtha- lic acid[7, 8], benzene tricarboxylic acid[9, 10], benzene tetracarboxylic acid[11, 12] and so on, those ligands …  相似文献   

13.
The title compound, {CdI2(2,2′-bipy)}n, was prepared by the hydrothermal reac- tion of CdI2 and 2,2′-bipy in an aqueous solution, and its crystal structure was determined by X-ray single-crystal analysis. Crystallographic data for 1: C10H8N2CdI2, monoclinic system, space group C2/c, a = 16.927(1), b = 10.0925(7), c = 7.7422(3) , β = 106.0629(4)°, V = 1271.00(14) 3, Z = 4, F(000) = 944, μ = 6.546 mm-1, Dc = 2.730 g/cm3, Mr = 522.38, the final R = 0.0309 and wR = 0.0805 for 1310 observed reflections (I > 2σ(I)). X-ray crystal structure analysis shows that the Cd atom is coordinated by four iodines and two N atoms from one 2,2′-bipy to form an 1-D chain-like structure through bridging iodines. The fluorescene of the title compound was also discussed.  相似文献   

14.
A new luminescent Cd(Ⅱ) compound, [Cd3(OABDC)2(bipy)2(H2O)2]n (1, H3OABDC = 5-oxyacetateisophthalic acid, bipy = 4,4'-bipyridine), has been prepared by the assembly of Cd(Ⅱ) salt with the mixed ligands of H3OABDC and 4,4'-bipy under hydrothermal conditions. The crystal structure is of monoclinic, space group P2/n with a = 13.6730(5), b = 10.1265(3), c = 15.9752(4) , β = 103.061(3)o, V = 2154.70(11) 3, C40H34Cd3N4O18, Mr = 1195.94, Z = 2, Dc = 1.843 g/cm3, F(000) = 1180, μ = 1.549 mm-1, the final R = 0.0409 and wR = 0.1291 for 2746 observed reflections (I > 2σ(I)). Single-crystal X-ray structural analysis reveals that compound 1 features a self-penetrating two-dimensional (2D) layered structure. According to topology analysis, this 2D framework can be characterized as a (3,4)-connected (6.72)2 (62.8)2 (73.8.102) net that has never been reported before. Finally, these 2D layers are further linked by intermolecular hydrogen bonds and π…π interactions to form a three-dimensional (3D) supramolecular framework. Moreover, Compound 1 exhibits strong blue photoluminescence at room temperature.  相似文献   

15.
A supramolecular complex of Cd(II) with 1D water tapes as pillars[Cd2(dpa)2(phen)2(H2O)2]·6H2O 1 (H2dpa = diphenic acid, phen = phenanthroline), has been synthesized and characterized by elemental analysis, IR spectroscopy, and single-crystal X-ray diffraction analysis. The crystal is of triclinic, space group P1^- with a = 9.7029(4), b = 11.9601(5), c = 12.1788(4) A, α = 71.6990(10), β = 71.8740(10), γ = 74.4680(10)°, V = 1252.39(8) A^3, C52H48Cd2N4O16, Mr = 1209.76, Z= 1, Dc = 1.604 g/cm^3,μ = 0.925 mm^-1, F(000) = 612, R = 0.0679 and wR = 0.2514 for 3870 observed reflections (I 〉 2σ(I)). Two intramolecular Cd(II) centers of this complex are encircled by two dpa^2- ligands forming an 18-membered ring, which is further assembled into a pillared three-dimensional (3D) supramolecular architecture through the synergetic effect of intermolecular face-to-face π…π stacking and weak O-H…O hydrogen-bonding interactions. Moreover, this complex exhibits photoluminescence with the main emission bands located at about 456 nm upon excitation at 355 nm in the solid state at room temperature.  相似文献   

16.
A new infinite three-dimensional framework structure of the title compound [H6MoVI8O27]·3C4N2H10 has been synthesized under mild hydrothermal conditions and charac-terized by elemental analyses,IR,fluorescent spectra and single-crystal X-ray diffraction.C12H36Mo8N6O27 crystallizes in the triclinic system,space group P 1 with a = 8.820(3),b = 9.534(3),c = 10.993(4) ,α = 99.985(17),β = 106.65(2),γ = 101.650(14)o,V = 840.6(5) 3,Mr = 1463.99,Z = 1,Dc = 2.892 g/cm3,μ = 2.993 mm-1,F(000) = 702,the final R = 0.0676,wR = 0.1920 and S = 1.074 for 2196 observed reflections with I > 2σ(I).The title compound exhibits a novel infinite three-dimensional(3D) framework composed of a [H6MoVI8O27] subunit and three dissociated piperazine fragments.The complex exhibits two strong fluorescent emission bands at ca.417 and 440 nm(λex = 378 nm) in the solid state at room temperature.  相似文献   

17.
WANG  Peng-Fei WU  Xiao-Shuo WU  Qiu-Yan WANG  Xin 《结构化学》2011,30(12):1709-1714
A novel interesting coordination polymer,[Cd(HSSA)(2-bimb)2].3H2O(1,H3SSA = 5-sulfosalicylic acid,2-bimb = 1,2-bis(imidazol-1-ylmethyl)-benzene),has been synthesized and structurally characterized.Compound 1 crystallizes in the monoclinic system,space group P21/n with a = 10.8653(10),b = 19.4100(17),c = 17.4414(17) ,β = 91.944(2)°,V = 3676.2(6) 3,Z = 4,C35H38CdN8O9S,Mr = 859.19,Dc = 1.552 g/cm3,μ = 0.717 mm-1,S = 0.999,F(000) = 1760,R = 0.0531 and wR = 0.1078.The compound features a rare three-dimensional(3D) 5-connected nov topology.In addition,compound 1 exhibits strong photoluminescent emission at room temperature.  相似文献   

18.
The reaction of CdCl3.2.5H2O with 3,5-pyrazoledicaiboxylic acid under hydrother-mal conditions produce a novel three-dimensional(3-D) coordination polymer [Cd2(C5H2O4N2)2.2H2O]n.The title compound crystallizes in the monoclinic system,space group P21/c with a = 6.422(4),b = 12.334(7),c = 8.936(6) ,β = 104.793(7)°,V = 684.4(7) 3,Z = 4,Dc = 2.761 g/cm3,μ = 3.181 mm-1,F(000) = 544,R = 0.0248 and wR = 0.0624.In the crystal structure of the title compround,molecules are linked through N-H...O hydrogen bonds,forming chains running along the a axis.Every Cd(Ш) coordinates with four molecules of ligand and one water molecule,forming a pentagomal-bipyramidal geometry.  相似文献   

19.
The title compound 2 (C30H27N3O, Mr = 445.55) has been synthesized and its structure was determined by X-ray crystallography method. The crystal is of monoclinic, space group P21/c with a = 17.520(15), b = 8.640(7), c = 15.439(13) , β = 98.642(14)°, V = 2310(3) 3, Dc = 1.281 g/cm3, μ = 0.780 mm-1, F(000) = 944, Z = 4, the final R = 0.0671 and wR = 0.1790 for 1952 observed reflections with I > 2σ(I). X-ray analysis revealed that the interatomic distance of C(20)O(1) is 1.464(4) , longer than that of the normal CO bond (1.41~1.43 ) in the six-membered heterocycle, but this kind of change coincides with other spiro compounds. The six-membered heterocycle containing spiro Csp3O is nonplanar. The UV-vis spectra of the title compound in polymer films showed that it exhibits excellent photochromic property.  相似文献   

20.
A new cadmium(II) compound, {[Cd[μ-(4,4'-dps)]2(H2O)2]·(4-abs)2(H2O)2}n 1 (4,4'-dps = 4,4'-dipyridylsulfide, 4-abs = deprotonated 4-amino benzenesulfonic acid), has been synthesized and structurally characterized. It belongs to the orthorhombic system, space group Pbcn with a = 19.950(3), b = 10.6381(13), c = 18.055(2) , V = 3831.8(8) 3, Z = 4, C32H36CdN6O10S4, Mr = 905.31, F(000) = 1848, μ = 0.850 mm-1, Dc = 1.569 Mg/m3 , the final R = 0.0238 and wR = 0.0589 for 3080 observed reflections with I > 2σ(I). Complex 1 is a one-dimensional linear chain coordination polymer and the repeat unit is comprised of doubly charged cadmium complex cation, uncoordinated 4-aminobenzene sulfonate anions and water molecules. The cadmium(II) ion adopts a six-coordinate distorted octahedral geometry. Complex 1 is stabilized and linked into a three-dimensional layered structure through intermolecular O–H···O and N–H···O hydrogen bonds together with electrostatic force. The cyclic voltammograms and fluorescence spectrum of 1 were also measured. It shows one irreversible redox process and emits a very strong and sharp fluorescent band at about 341 nm.  相似文献   

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