Synthesis, Crystal Structure and Photoluminescence of a Zn(Ⅱ) Coordination Polymer Derived from 1,1'-Biphenyl-2,2',6,6'-tetracarboxylic Acid

A new polymeric znic（II） coordination polymer, [Zn2（bptc）·（H2O）4]n·nC H3 OH 1, was synthesized by the hydrothermal reaction of Zn（NO3）2·6H2O with 1,1＇-biphenyl-2,2＇,6,6＇-tetracarboxylic acid（H4bptc） and structurally characterized by single-crystal diffraction, IR and elemental analysis. The polymer crystallizes in the orthorhombic system, space group Pnna with a = 13.411（1）, b = 16.418（2）, c = 9.178（7）, V = 2025.2（3） 3, Z = 4, C17H14O13Zn2, Mr = 557.06, Dc = 1.827 g/cm3, F（000） = 1120, μ（MoK α） = 2.439 mm-1. The final R and wR are 0.0548 and 0.1691 for 1279 observed reflections with I 2（I）. In this compound, the bptc4- anion adopts monodentate bridging coordination modes connecting the zinc（II） ions to form a 1D chain structure, which furnishes a 2D supramolecular architecture through hydrogen bonding interactions formed by carboxylic oxygen atoms of bpdc, oxygen atoms of crystalline methanol and water molecules. Complex 1 displays an emissive maximum at 435 nm in the solid state at room temperature.

Syntheses,Crystal Structures and Thermal Stabilities of Two New Mixed Ligated Coordination Polymers with Rigid Dicarboxylate and Flexile N-donor Ligands

Two new coordination polymers,[Co（BIPA）（bpp）]（1） and [Zn（BIPA）（bpp）（H2O）]（2）（H2BIPA = 5-bromoisophthalic acid,bpp = 1,3-di（4-pyridyl）propane） have been synthesized via hydrothermal reactions.The two compounds were characterized by elemental analysis,IR spectra,TG analysis and single-crystal X-ray determination.Compound 1 crystallizes in triclinic,space group P1 with a = 9.0316（13）,b = 10.1179（14）,c = 11.8884（17） ,α = 68.022（2）,β = 84.749（2）,γ = 77.791（2）°,V = 984.5（2） 3,Z = 2,C21H17BrN2O4Co,Mr = 500.21,Dc = 1.687 g.cm-3,μ = 2.932 mm-1,S = 0.981,F（000） = 502,R = 0.0440 and wR = 0.1357 for 3773 observed reflections with I 2σ（I）.Compound 2 crystallizes in the monoclinic system,space group P21/c with a = 7.8466（10）,b = 27.483（4）,c = 9.6583（13） ,β = 96.663（3）°,V = 2068.8（5） 3,Z = 4,C21H19BrN2O5Zn,Mr = 524.66,Dc = 1.685 g.cm-3,μ = 3.155 mm-1,S = 0.969,F（000） = 1056,R = 0.0441 and wR = 0.0517 for 4058 observed reflections with I 2σ（I）.The two compounds are constructed from the BIPA2-and bpp ligands but they exhibit different kinds of one-dimensional chain structures.In 1,the chains are composed of the Co（Ⅱ） ions and BIPA2-ligands,and the chains are further extended into a 2D framework structure by π...π interactions of the benzene rings from the BIPA2-ligands between the adjacent chains.In 2,the chains are made up of Zn（Ⅱ） ions and BIPA2-ligands through another fashion,and the chains are further linked via hydrogen bonding interactions to yield a two-dimensional supramolecular layer structure.Furthermore,the bpp ligand features two kinds of different coordination modes in the two compounds.

Synthesis, Crystal Structure and Photoluminescence of a Copper(Ⅰ)-iodide Coordination Polymer Based on Polyimidazolate Ligand

A copper(Ⅰ)-iodide coordination polymer,namely{[Cu3 I3(Tipa)2]·3(DMF)}n(1),was synthesized from tetrahedral Cu4 I4(py)4 precursor and tris(4-(~1H-imidazol-1-yl)phenyl)amine)(Tipa)ligand in N,N-dimethylformamide(DMF)and methanol,and characterized by single-crystal X-ray diffraction.Its crystal crystallizes in monoclinic system,space group P2/c with a=12.849(4),b=12.034(3),c=24.619(7)A,β=104.681(4)°,Mr=1604.52,V=3682.4(18)A^3,Z=2,Dc=1.447 g/cm^3,μ=2.163 mm^-1,S=0.975,F(000)=1580,the final R=0.0835 and wR=0.2354 for 6471 observed reflections(I>2σ(I)).In compound 1,the Cu4 I4(py)4 was in-situ changed into another neutral CuI unit.Interestingly,two CuI units and two imidazole rings of the tipa ligands form a macrocyclic loop,which are further linked by another CuI unit and the third imidazole ring of the tipa ligands to produce a 1 D loop-containing chain.Solvent molecules were filled in the pore of the loop,which prevents the interpenetration of each other.The packing of these 1 D chains generates a 1 D channel along the a-axis,which is filled by disordered DMF molecules.In addition,compound 1 exhibits high thermal stability and strong photoluminescence at room temperature.

A Zinc(Ⅱ) Coordination Polymer Based on a Polycarboxylate Ligand: Synthesis, Crystal Structure, Photoluminescence and Photocatalysis

A new zinc coordination polymer(CP) {[Zn1.5(ttb)0.5(phen)(H2O)]·2 H2O}n(1),(H6ttb = 3,4,5-tricarboxyl-(3',4',5'-tricarboxylazophenyl)benzene, phen = 1,10-phenanthroline), has been hydrothermally synthesized and structurally characterized by single-crystal X-ray determination, IR and thermogravimetric analysis(TGA). CP 1 crystallizes in the monoclinic system, space group C2/c with a = 12.402(3), b = 15.231(3), c = 22.233(4)A, β = 94.388(3)°, Zn1.5C21H16N3O9, Mr = 552.42, V = 4187.3(15) A^3, Dc = 1.753 g/cm^3, F(000) = 2240, μ = 1.795 mm^-1, S = 1.041, GOF = 1.041, Rint = 0.0169, 2.36°<θ<30.95°, and Z = 8. The final refinement gave R = 0.0340 and w R = 0.0927 for 5791 observed reflections with I > 2σ(I). The completely deprotonated(ttb)^6- ion in 1 adopts an octadentate coordination mode(μ8-η^2-η^1-η^1-η^1-η^1-η^2). Four of the carboxyl groups are coordinated with four zinc ions by monodentate, respectively. While the other two carboxyl groups are coordinated with four zinc ions by bidentate, respectively. So, CP 1 possesses a 3 D network structure cross-linked by(ttb)6-ion. The XRD, UV and photoluminescence properties of CP 1 were also studied. Remarkably, 1 exhibits photocatalytic activities for the degradation of dye(MO) under UV light irradiation and shows good stabilities towards UV-light photocatalysis.

Synthesis,Crystal Structure and Photoluminescence Property of a Ni(Ⅱ) Coordination Polymer with One-dimensional Double-sinusoidal Structure

A new coordination polymer [Ni（3-bpo）（m-bdc）（C2H5OH） 2]n（1,3-bpo = 2,5-bis（3-pyridyl） -1,3,4-oxadiazole,m-H2bdc = 1,3-benzenedicarboxylic acid） was solvothermally synthesi-zed and characterized by IR,TGA and single-crystal X-ray diffraction. The title complex crystalli-zes in the orthorhombic system,space group Pnma with a = 7.786（3） ,b = 17.253（6） ,c = 18.478（6） ,V = 2481.9（14） A^3,Mr = 539.18,Dc = 1.443 g/cm^3,Z = 4,R = 0.0353 and wR = 0.0589. The m-bdc and 3-bpo bridge two Ni（Ⅱ） ions through two carboxylate groups and two pyridyl groups forming a 1D infinite double-sinusoidal chain along the c axis. The photoluminescence of 1 shows a large red shift compared to that of free ligands in the solid state.

Synthesis,Crystal Structure and Thermal Behavior of a New 2D Barium(Ⅱ) Coordination Polymer with 1H-benzimi-dazole-5,6-dicarboxylate as the Single Ligand

The self-assembly of 1H-benzimidazole-5,6-dicarboxylic acid with barium chloride under hydrothermal conditions afforded a new 2D coordination polymer,[Ba2（L）（HL）Cl]n（1,L = 1H-benzimidazole-5,6-dicarboxylate）,which was characterized by elemental analysis,infrared spectroscopy,thermogravimetric analysis,and single-crystal X-ray diffraction.Compound 1 is of monoclinic system,space group P21/c with a = 10.0145（6）,b=25.6854（15）,c=7.3116（4） ？,β = 99.4980（10）°,V = 1854.95（19）3,C18H9Ba2ClN4O8,Z = 4,Mr=719.42,Dc = 2.576 g/cm3,μ（MoKα） = 4.427 mm-1,F（000） = 1352,the final R = 0.0202 and wR=0.0465 for 3051 observed reflections with I 2σ（I）.It exhibits an interesting two-dimensional network structure and high thermal stability（up to 420 ℃）.

Solvothermal Synthesis,Crystal Structure and Photoluminescence Property of a 3D Lead(Ⅱ)Coordination Polymer Based on Terephthalic Acid

Solvothermal reaction of Pb（NO3）2·6H2O with rigid linear ligand terephthalic acid（H2pta） in N,N-dimethylformamide（DMF） produced a new three-dimensional（3D） lead（Ⅱ）coordination polymer[Pb2（pta）1.5（μ4-OH）（DMF）]n 1,and its structure was characterized by single-crystal X-ray diffraction analyses.In polymer 1,the μ4-OH bridges the nearby lead（Ⅱ） ions into an infinite one-dimensional（1D） chain,and then the organic ligand pta^2- joins the neighbored chains into a 3D structure by two similar connection modes in different configurations.The solid-state photoluminescent studies revealed that 1 exhibits a strong greenish emission mainly originating from ligand-to-metal charge transfer between the delocalized π bonds of the aromatic carboxylate ligand pta^2- and the p orbitals of the Pb^2＋ centers.

A Cd(Ⅱ) Coordination Polymer Containing 4-(1-H-imidazol-2-yl) Benzoic Acid Ligand: Synthesis, Crystal Structure, and Photoluminescence Property

A new cadmium（II） polymer based on imidazole derivative, formulated as [Cd（Hiba）2]n 1, H2iba = 4-（1-H-imidazol-2-yl） benzoic acid）, has been synthesized under hydro- thermal conditions. The compound crystallizes in triclinic system, space group P1 with a = 7.062（4）, b = 10.840（7）, c = 13.099（8） A, a = 98.102（7）, fl = 101.524（7）, y = I07.961（7）°, V= 912.3（10） A3, Z = 2, Mr = 486.75, Dc = 1.772 Mg/m3,/t = 1.234 mm-1, F（000） = 484, the final R = 0.0735 and wR = 0.1739 for 2154 observed reflections with 1 〉 20（I）. Polymer 1 consists of （Cd-Hiba）2 zigzag chains, which are further linked by hydrogen bonding to extend into a two-dimensional （2D） corrugated-shape sheet structure. The 2D structures are further connected into a 3D supramolecular edifice through hydrogen bonding. The polymer exhibits exceptional high thermal stability. The bulk purity of the materials of 1 was confirmed through the powder X-ray diffraction （PXRD） patterns. The luminescent property of polymer I has also been investigated.

Synthesis and Crystal Structure of a New Three-dimensional Coordination Polymer:[Mn(2,3-pdc) (H_2O)]_n (2,3-pdc=Pyridine-2,3-dicarboxylate)

A new three-dimensional coordination polymer [Mn（2,3-pdc）（H20）]n （2,3-pdc = pyridine-2,3-dicarboxylate） 1 has been hydrothermally synthesized and structurally characterized. The crystal belongs to the monoclinic system, space group P21/c with a = 6.4168（5）, b = 10.7939（9）, c = 11.1549（10） A, β = 94.733（4）°, V = 769.98（11） A3, Z = 4, Mr = 238.06, De = 2.054 g/cm3, μ（MoKa） = 1.707 mm-1, F（000） = 476, Rint = 0.0326; R = 0.0499 and wR = 0.1636 for 1564 observed reflections with I 〉 2σ（I）. X-ray diffraction analyses reveal that the title compound is a three-dimensional coordination polymer consisting of one MnⅡ center with a distorted octahedral environment arranged by four 2,3-pdc ligands and one water molecule.

Synthesis, Crystal Structure, Thermal Behavior and Photoluminescence of a Novel Two-dimensional Cd(Ⅱ) Coordination Polymer

A new coordination polymer, [Cd2（bptc）（L）2（H2O）2]·5H2O（1, L = 2-（2-chloro-6-fluorophenyl）-1H-imidazo[4,5-f][1,10]phenanthroline and H4 bptc = 3,3＇,4,4＇-biphenyltetracarboxylic acid）, has been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P21/n with a = 18.868（4）, b = 7.2111（14）, c = 19.464（4）A, β = 95.75（3）°, C54H31Cd2Cl2F2N8O15, Mr = 1365.57, V = 2635.0（9）A3, Z = 2, Dc = 1.721 g/cm^3, S = 1.034, μ（MoKα） = 0.995 mm^–1, F（000） = 1358, R = 0.0501 and wR = 0.1076. In 1, each bptc anion bridges four Cd（II） atoms to form 2D layer structures, which are further extended by π-π stacking interactions into a 3D supramolecular architecture. The thermal behavior and luminescent properties of the compound have also been studied.

A Novel 6-Connected Self-interpenetrated Zn(Ⅱ) Coordination Polymer Based on 1,4-Bis(2-methylimidazole-3-ium-1-yl)biphenyl and Dicarboxylate Ligand: Synthesis, Crystal Structure and Luminescent Property

A novel coordination polymer {[Zn2（pda）2（bmp）1.5]·2H2O}n（1, H2 pda = 1,4-phenyl enediacetic acid and bmp = 1,4-bis（2-methy limidazol-3-ium-1-yl）biphenyl） was synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectroscopy and powder X-ray diffraction（PXRD）. Complex {[Zn2（pda）2（bmp）1.5]·2H2O}n（1） is of triclinic system, space group P1 with a = 10.132（5）, b = 11.854（5）, c = 18.784（5） A, α = 80.256（5）, β = 75.163（5）, γ = 75.620（5）°, Z = 2, V = 2099.0（15） A3, Mr = 908.54, Dc = 1.437 g/cm^3, F（000） = 938 and μ = 1.206 mm-1. The final R = 0.0541 and wR = 0.1397 for 8017 observed reflections with I 2σ（I）. Complex 1 displays a three-dimensional（3D） self-interpenetrated 6-connected topological net with point symbol（48.67）. Furthermore, the luminescent property of complex 1 was investigated in the solid state at room temperature.

Crystal Structures and Photoluminescent Properties of Two Cd^(2＋) Coordination Polymers Constructed from an 8-Hydroxyquinolinate Ligand

In order to perform a study on the structural modulation in the Cd（Ⅱ）-L architecture（HL =（E）-2-[2-（3-pyridyl）ethenyl]-8-hydroxyquinoline）, two different dicarboxylic acids, namely, 2-aminoterephthalic acid（H_2ATA） and 4,4￠-biphenyldicarboxylic acid（H_2BPDC）, are employed as the secondary auxiliary ligands. Two new complexes [Cd_2L_2（ATA）]（1） and [Cd_2L_2（BPDC）·2MeO H· 4H_2O]（2） with distinct 3D frameworks were obtained. In complex 1, ligands ATA bridge the 1D Cd（Ⅱ）-L infinite chains into a 3D polymeric coordination network. Complex 2 is a 3D porous framework, in which adjacent 2D Cd（Ⅱ）-L coordination layers were linked together by the coor- dinated BPDC ligands. The variant structures of two complexes indicate that the skeleton of dicarboxylate anions plays a great role in the assembly of such different frameworks. In addition, the photoluminescent properties（fluorescent emission, lifetime, and quantum yield） of polymers 1 and 2 were also investigated in the solid state.

Synthesis and Crystal Structure of a Two-dimensional Coordination Polymer Constructed by Thiophene-2,5-dicarboxylic Acid and 1,4-Bis(imidazol-1-yl)-butane

A metal-organic coordination polymer [Cd（tdc）（bimb）（μ2-H2O）]n （H2tdc = thiophe-ne-2,5-dicarboxylic acid, bimb = 1,4-bis（imidazol-l-yl）-butane） 1 has been hydrothermally synthe- sized and characterized by elemental analysis, IR, TG, luminescence spectrum and single-crystal X-ray diffraction. Colorless crystals crystallize in the triclinic system, space group P^-1 with a = 5.8945（3）, b = 10.3129（5）, c = 11.2226（5） A, a = 95.1430（10）,β = 97.9020（10）, γ = 90.5910（10）°, V = 672.84（6） A^3, C11H11CdN2O5S, Mr= 395.68, De = 1.953 g/cm^3, μ（MoKa） = 1.797 mm^-1, F（000） = 390, Z = 2, the final R = 0.0209 and wR = 0.0508 for 2514 observed reflections （I 〉 2σ（I））. The structure of 1 exhibits a two-dimensional layer-like structure.

Synthesis, Crystal Structure and Electrochemical Properties of a One-dimensional Chain Coordination Polymer [Cu(phen)(2,4,6-TMBA)_2(H_2O)]_n

A one-dimensional chain coordination polymer [Cu（phen）（2,4,6-TMBA）2（H2O）]n has been synthesized by reacting 2,4,6-trimethyl-benzoic acid, 1,10-phenanthroline and Cu（Ⅱ） perchlorate and its structure was characterized. Crystal data for this complex： tetragonal, space group I41, a = 2.0293（3）, b = 2.0293（3）, c = 1.3758（2） nm, α =β= γ = 90°, V= 5.6657（13） nm3, Dc= 1.379 g/cm3, Z = 8, μ（MoKa） = 0.815 mm-1, Mr = 588.14, F（000） = 2456, S = 1.047, R = 0.0459 and wR = 0.1053. The crystal structure shows that two neighboring Cu（Ⅱ） ions are linked together by one bridging-chelating 2,4,6-trimethyl-benzoic group, forming a one-dimensional chain structure. Each Cu（Ⅱ） ion is coordinated with two nitrogen atoms from one 1,10-phenanthroline molecule, three oxygen atoms from three 2,4,6-trimethyl-benzoic acid molecules and one oxygen atom from one water molecule, giving a six-coordinate distorted octahedral coordination geometry. The cyclic voltammetry behavior of the complex was also investigated.

Synthesis and Crystal Structure of a New Two-dimensional Manganese Coordination Polymer:[Mn(L)(1,4-bdc)]

A new coordination polymer, [Mn（L）（1,4-bdc）] （L = 11-fluoro-dipyrido[3,2- a：2＂,3 ＂- c]phenazine, 1,4-bdc - benzene-1,4-dicarboxylate）, has been synthesized through the hydrothermal method and characterized by elemental analysis, IR and single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 9.7544（9）, b = 10.8254（10）, c = 11.5288（10） A, a = 114.1300（10）, β = 96.6110（10）, y = 105.0390（10）°, V= 1038.62（16）/k3, Z= 2, C26H13FMnN404, Mr = 519.34, Dc = 1.661 g/cm3, F（000） = 526, ,u（MoKa） = 0.691 mm^-, R = 0.0405 and wR = 0.0977. The 1,4-bdc dianions link the neighboring Mn（II） atoms to yield a two-dimensional layer structure. The L ligands are attached on both sides of the layer. The π-π interactions between the L ligands of neighboring layers result in a three-dimensional supramolecular architecture.

Hydrothermal Synthesis, Crystal Structure and Photoluminescent Property of a Zinc(II) Coordination Polymer Assembled by Phthalate and 4,4′-Bipyridine

A metal-organic coordination polymer {[Zn（Pht）（4,4＇-bipy）（H2O）2]·2H2O}n （Pht = phthalate, 4,4＇-bipy = 4,4＇-bipyridine） 1 has been hydrothermally synthesized and characterized by elemental analysis, IR, TG, fluorescence spectrum and single-crystal X-ray diffraction. Yellow crystals crystallize in the monoclinic system, space group P2/n, a = 7.6346（14）, b = 11.316（2）, c = 10.8133（19） ,A, β = 92.A.A,A.（3）°, V = 933.3（3） A^3, C18H20N2O8Zn, Mr = 457.73, Dc = 1.629 g/cm^3, F（000） = 472, Z = 2,μ（MoKa） = 1.367 mm^-1, the final R = 0.0323 and wR = 0.0821 for 1859 observed reflections （Ⅰ〉 2σ（Ⅰ））. The structure of 1 exhibits a two-dimensional bilayer framework formed by hydrogen bonding interactions. Furthermore, 1 shows yellow photoluminescent property at room temperature.

Synthesis, Crystal Structure and Luminescent Property of a Ag(Ⅰ) Coordination Polymer with a 3D Sandwich-like Framework

A new coordination polymer,{[Ag2（bpp）2（H2O）2]·bpdc·3H2O}n,derived from the ligand biphenyl-4,4＇-dicarboxylic acid（H2bpdc）,has been obtained through a hydrothermal technique（bpp = l,3-bis（4-pyridyl）propane）.Its single-crystal structure has been characterized by single-crystal X-ray diffraction,powder XRD,FT-IR,TGA and elemental analysis techniques.The single-crystal X-ray diffraction reveals that complex 1 consists of 1D infinite[Ag（bpp）（H2O）]n^（n＋）cationic chains,2D anionic layer constructed by bpdc anions and free water which provide charge compensation in the crystal structure.The 1D infinite[Ag（bpp）（H2O）]n^（n＋） cationic chains and 2D anionic layer are further stacked in-ABAB- fashion through intermolecular H-bonding to form a 3D sandwich-like framework.In addition,the luminescent property of complex 1 in the solid state at room temperature was investigated.

Synthesis,Crystal Structure and Photoluminescence of a New Zn(Ⅱ) Dimer Constructed by 1,10-Phenanthroline Derivative and Flexible Dicarboxylate

A new compound, [Zn（L）（1,4-chdc）]2-2H20 （1, 1,4-chdc = 1,4-cyclohexanedicar- boxylate and L = 11-fluoro-dipyrido[3,2-a：2＂,3＂-c]phenazine）, has been synthesized under hydro- thermal conditions and characterized by single-crystal X-ray diffraction. The crystal of I belongs to triclinic, space group P1 with a = 9.4679（19）, b = 10.915（2）, c = 12.577（3）/k, a = 77.22（3）, β = 74.73（3）, y = 65.47（3）°, C52H39F2NsO10Zn2, M,. = 1104.65, V = 1131.4（4） A3, Z = 1, Dc = 1.621 g/cm3, S = 1.091, μ（MoKa） = 1.143 mm-1, F（000） = 565, R = 0.0426 and wR = 0.1171. In 1, two 1,4-chdc anions bridge two Zn（II） atoms to form a dimer. The neighboring dimers are further extended by π-π stacking interactions to form a 2D supramolecular layer. The luminescent property of the compound has also been investigated.

Hydrothermal Synthesis and Crystal Structure of a Cobalt(II) Coordination Polymer: [Co(C_2O_4)(bix)]_n (bix = 1,4-Bis(imidazol-1-ylmethyl)-benzene)

A new two-dimensional cobalt coordination polymer has been prepared and fully characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. The compound [Co（C2O4）（bix）]n 1 crystallizes in the monoclinic system, space group C2/c, with a = 11.549（3）, b = 15.700（3）, c = 9.260（2） A, β = 102.984（3）°, V = 1636.0（6） A^3, C16HIaCON4O4, Mr= 383.23, Dc = 1.556 g/cm^3, μ（MoKa） = 1.078 mm^-1, F（000） = 780, Z = 4, the final R = 0.0455 and wR = 0.1286 for 1483 observed reflections （I 〉 2σ（I））. Of the compound, the Co center is octahedrally coordinated with oxalate acting as a tetra-dentate ligand coordinated to the cobalt atom and each bix serving as a bridging ligand by employing two N-donors to coordinate with the Co center. An infinite {Co2（C2O4）2}∞ chain is formed along the α axis. Furthermore, the 1D chains are held together via bix ligands to generate a two-dimensional network structure with 1D coronal-like channels （ca. 5.691A × 15.700A）.

Urothermal Synthesis and Crystal Structure of a Zn(Ⅱ) Coordination Polymer with a 3-D Supramolecular Structure

A new metal-organic coordination polymer [Zn（hfipbb）（e-urea）]n（1,H2hfipbb = 4,4＇-（hexafluoroisopropylidene）bis（benzoic acid）,e-urea = ethylene urea） has been urothermally synthesized and characterized by elemental analysis and single-crystal X-ray diffraction.The title complex crystallizes in monoclinic,space group P21/c with a = 13.302（4）,b = 10.981（3）,c = 13.804（4） ,β = 93.587（5）°,V = 2012.3（10） 3,C20H14N2O5F6Zn,Mr = 541.72,Z = 4,Dc = 0.447 g/cm3, = 0.328 mm-1,F（000） = 272,R = 0.0340 and wR = 0.1107 for 4528 observed reflections（I 〉2σ（I））.In the structure of compound 1,two Zn（Ⅱ） ions are bridged by two carboxylate groups from two hfipbb ligands to form a dinuclear unit,and each dinuclear Zn（Ⅱ） unit is linked with its two adjacent dinuclear units through four hfipbb ligands into an infinite one-dimensional double-chain.The interesting structural feature of compound 1 is that the one-D double-chains are self-interconnected into a three-D supramolecular structure through hydrogen bonds between the coordinated e-urea molecules and carboxylate oxygen atoms（N1 and O2,N2 and O4）.