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.

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.

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）.

Synthesis, Crystal Structure and Photoluminescent Property of a Three-dimensional Zinc(Ⅱ) Coordination Polymer: [Zn_1.5(PDB)(bix)_0.5(μ_2-OH)]_(2n)

A new metal-organic coordination polymer [Zn1.5（PDB）（bix）0.5（μ2-OH）]2n 1 （H2PDB = pyridine-3,4-dicarboxylic acid, bix = 1,4-bis（imidazol-1-ylmethyl）-benzene） has been hydrothermally synthesized and structurally characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. The title compound crystallizes in the monoclinic system, space group P2/c with a = 7.411（2）, b = 7.848（3）, c = 25.048（8）, V = 1451.8（8）3, C28H22N6O10Zn3, Mr = 798.63, Dc = 1.827 g/cm3, μ（MoKα） = 2.529 mm-1, F（000） = 804, Z = 2, the final R = 0.0440 and wR = 0.1035 for 1952 observed reflections （I 2σ（I））. It exhibits a three-dimensional framework structure. Moreover, its luminescent property has been investigated in the solid state.

Hydrothermal Synthesis and Crystal Structure of a New 2D Mn(II) Coordination Polymer with 4,4′-Sulfonyldi Benzoic Acid and 1,4-Bis(imidazol-1-ylmethyl) benzene Ligands

A novel manganese coordination polymer [Mn2（sfdb）2（biyb）2（H2O）2]n （1, H2sfdb = 4,4′-sulfonyldibenzoic acid, biyb = 1,4-bis（imidazol-1-ylmethyl）benze） has been hydrothermally synthesized and structurally characterized by single-crystal X-ray determination, IR and thermogravimetric analysis （TGA）. Complex 1 crystallizes in the triclinic system, space group Pi with a = 10.138（4）, b = 11.187（5）, c = 13.582（6） A, α = 69.146（7）, β = 89.628（7）, γ = 77.076（7）°, MnzC56H48N8O14S2, Mr= 1231.02, V= 1398.5（10） A3, Dc= 1.462 g/cm3, F（000） = 634,μ = 0.600 mm-1, S = 1.088 and Z = 1. The final refinement gave R = 0.0570 and wR = 0.1229 for 4889 observed reflections with 1 〉 2σ（I）. Interestingly, in complex 1, the sfdb2 and biyb ligands connect the Mn（Ⅱ） ions into two-dimensional 2-fold interpenetrating layers, and such layers are further connected with each other to generate a 3D supramolecular structure through hydrogen bonding interaction.

Hydrothermal Synthesis and Crystal Structure of a Three-dimensional Nickel(II) Coordination Polymer: [Ni_2(NIPH)_2(bimb)_(2.5)(H_2O)]n·3nH_2O

A new metal-organic coordination polymer [Ni2（NIPH）2（bimb）2.5（H2O）] n·3nH2O 1 （H2NIPH = 5-nitroisophthalic acid, bimb = 1,4-bis（imidazol-1-yl）-butane） has been hydrothermally synthesized and structurally characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. The title complex crystallizes in the orthorhombic system, space group P4（1）2（1）2 with a = 17.3533（16）, b = 17.3533（16）, c = 30.802（6）A, V= 9275（2）A^3, C41HagN12Ni2O16, Mr = 1083.34, Dc = 1.552 g/cm^3, p（MoKa） = 0.897 mm^-1, F（000） = 4504, Z = 8, the final R = 0.0383 and wR = 0.0952 for 7343 observed reflections （I〉 2σ（I））. It exhibits a three-dimensional network structure.

Synthesis and Crystal Structure of a Novel 2D Coordination Polymer [Cu_3(mal)_2(di-2-pyridlyktone)_2]

A novel coordination polymer of Cu II with flexible ligands,namely,[Cu 3 （mal） 2 （di2-pyridlyktone） 2 ] （1,H 2 mal=maleic acid）,was synthesized and characterized by single-crystal X-ray diffraction,thermogravimetric analyses,elemental analysis and IR spectroscopy.The structure indicates that the complex crystallizes in monoclinic,space group P2 1 /c with a=10.268（2）,b=17.737（3）,c=8.038（1）,β=98.275（2）°,V=1448.6（4） 3,Z=2,D c=1.883 Mg·m-3,μ=2.260 mm-1,F（000）=826,and the final R=0.0321 and wR=0.0820.In 1,three Cu II centers （Cu（1）,Cu（2）,Cu（1A）） are bridged by two uncommon μ 3-bridging H 2 mal ligands,furnishing a centrosymmetric trimetallic unit.Via further Cu-O COO coordination interactions,extention of these trimetallic units in two directions gives rise to an infinite corrugated 2D layer.In addition,thermal stability and electrochemistry of 1 were studied.

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 ℃）.

Synthesis and Crystal Structure of a New(6,3)-Connected Ni(Ⅱ) Coordination Polymer

The coordination polymer [Ni（dpa）（bpp）]n（H2dpa = 2,4＇-biphenyl-dicarboxylic acid,bpp = 1,3-di（4-pyridyl）propane） was hydrothermally prepared and characterized by single-crystal X-ray diffraction,FTIR spectra,elemental analysis and thermal analysis.The crystal is of triclinic system,space group P1 with a = 12.516（5）,b = 12.943（5）,c = 15.130（5） ,α = 94.331（5）,β = 91.827（5）,γ = 108.382（5）°,C54H44N4Ni2O8,Mr = 497.18,V = 2315.3（15） 3,Dc = 1.426 g/cm3,F（000） = 1032,μ = 0.875 cm-1,Z = 2,the final R = 0.0496 and wR = 0.1100 for 5365 reflections with Ⅰ 〉 2σ（Ⅰ）.X-ray diffraction analysis reveals that the carboxylate group of 2,4＇-diphenic acids acting as bridging ligands adopts two coordination modes：bis-mondentate and bidentate chelating.The compound exhibits a two-dimensional（6,3）-connected architecture.

Synthesis and Crystal Structure of a Three-dimensional Mn(Ⅱ) Coordination Polymer with 3-(Pyrazin-2-yloxy)-pyridine and Azide Anion as Mixed Bridge Ligand

A three-dimensional coordination polymer [Mn2（μ1.3-N3）4（μ-PP）2]n （PP = 3-（pyrazin-2-yloxy）-pyridine） has been synthesized with 3-（pyrazin-2-yloxy）-pyridine and azide anion as mixed bridge ligand, and its crystal structure was determined by X-ray crystallography. The crystal data： triclinic system, space group P1, with a = 6.794（4）, b = 9.885（6）, c = 9.947（6） A, α = 64.170（6）, β= 84.190（8）, γ= 85.319（8）°, V = 597.7（6）A^3, Z = 1, C18H14Mn2N18O2, Mr = 624.35, Dc = 1.735 g/cm^3, F（000） = 314 and μ = 1.117 mm^-1. In the crystal, the azide anion acts as a bridge ligand and makes adjacent Mn（Ⅱ） ions connect into a two-dimensional sheet on the ab plane, then 3-（pyrazin-2-yloxy）-pyridine serves as a bidentate bridge ligand to connect neighboring sheets along

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 2D Cobalt(Ⅱ) Coordination Polymer [Co(iqnc)_2]_n: Synthesis, Crystal Structure and Characterization

A new cobalt（Ⅱ） coordination polymer with the formula of [Co（iqnc）2]n（1, iqnc = l-isoquinolinecarboxylate） has been synthesized through hydrothermal synthesis and structurally characterized by single-crystal X-ray diffraction method. The title coordination polymer represents a two-dimensional layer structure featuring adjacent one-dimensional [Co（iqnc）2]n chains connected with each other by uncoordinated oxygen atoms of carboxylate. Crystal data： monoclinic, space group P21/c, a = 15.4302（2）, b = 5.6743（7）, c = 9.2307（1） A, β = 98.459（2）o, V = 799.41（2） A3, Z = 2, S = 1.019, the final R = 0.0346, w R = 0.0876（I 2σ（I）） and R = 0.0477 and wR = 0.1159 for all reflections. In addition, elemental analysis, IR, and magnetism properties are presented.

Synthesis and Crystal Structure of a Novel Manganese Coordination Polymer Constructed by 3,5-Dimethylbenzoic Acid with 4,4'-Bipyridine

A novel manganese coordination polymer [Mn（L）2（bipy）]n （HL = 3,5-dimethylbenzoic acid, 4,4＇-bipy = 4,4＇-bipyridine） has been synthesized by a hydrothermal method. The molecular and crystal structures were determined by single-crystal X-ray diffraction. The crystal is of monoclinic, space group C2/c with a = 2.0996（8）, b = 1,1835（5）, c = 0.9958（4） nm, β = 110.161（5）°, V = 2,3229（16） nm^3, Z = 4, C28H26MnN2O4, Mr = 509.45, Dc= 1.457 g/cm^3,μ = 0.607 mm^-1, F（000） = 1060, Rim = 0.0566, R = 0.0334 and wR = 0.1078. In the crystal the manganese atom is six-coordinated by two nitrogen atoms from 4,4＇-bipy and four oxygen atoms from 3,5-dimethylbenzolate molecules, completing an octahedral geometry. The 4,4＇-bipy molecules bridge the infinite chain [Mn（L）2（bipy）]n to form a two-dimensional layer.

One New Zinc Coordination Polymer Based on 2-Chloro-benzoate and 4,4'-Bipyridine: Synthesis, Crystal Structure and Luminescence

A Zn-based coordination polymer [Zn（2-cb）2（4,4′-bpy）0.5]n （1, 2-cb = 2-chloro- benzoate, 4,4＇-bpy = 4,4′-bipyridine） was prepared by hydrothermal synthesis using 2-chloro- benzoic acid and 4,4′-bipyridyl as ligands. The compound was characterized by elemental analysis, IR, TGA, and X-ray single-crystal diffraction. The crystal belongs to the monoclinic system, space group PI with a = 8.0471（5）, b = 9.7338（6）, c = 11.7830（7） A, a = 96.2230（10）, β = 92.542（2）, γ = 103.7560（10）°, V = 888.84（9） A3, Z = 2, Mr = 454.57, Dc = 1.698 g/cm3,μ（MoKa） = 1.708 mm.1, F（000） = 458, the final R = 0.0359 and wR = 0.0936 for 3167 observed reflections with I 〉 2σ（I）. The crystal analysis indicates that 1 exhibits a 1-D chain structure constructed by 4,4′-bpy and a dicaryon secondary-building-unit of [Zn2（2-cb）4]. Luminescence analysis revealed that compound 1 emits blue fluorescence with a fluorescence lifetime of 55.03 ns.

A One-dimensional Manganese(Ⅱ) Coordination Polymer with 4'-Hydroxybiphenyl-4-carboxylate as the Single Ligand:Synthesis,Crystal Structure and Luminescence

A new 1D coordination polymer,{[Mn2（4＇,4-hbc）4（4＇,4-Hhbc）2（H2O）]·H2O}n（4＇,4-Hhbc=4＇-hydroxyl-biphenyl-4-carboxylic acid）,has been hydrothermally synthesized and struc-turally characterized by elemental analysis,IR spectroscopy and single-crystal X-ray diffraction.The crystal belongs to the monoclinic system,space group C2/c with a=52.421（10）,b=7.5388（15）,c=16.478（3）,β=106.12（3）°,V=6256（2）3,Z=4,C78H62Mn2O21,Mr=1445.16,Dc=1.534g/cm3,μ（MoKα）=0.490mm-1,F（000）=2992,R=0.0764 and wR=0.2006 for 2984 observed reflections with I2σ（I）.X-ray diffraction analyses reveal that the title compound is a one-dimensional infinite chain,in which the MnⅡ atom adopts a distorted octahedral geometry coordinated by four 4＇,4-hbc ligands,one 4＇,4-Hhbc ligand and one water molecule.Furthermore,the luminescent property of title compound was investigated.

Hydrothermal Synthesis and Crystal Structure of a 2D Zinc(Ⅱ) Coordination Polymer with 5-Hydroxynicotinic Acid

The title compound, [Zn（5-hydroxynicotinate）22H2O]n, has been synthesized by reacting zinc sulfate vitriol with 5-hydroxynicotinic acid under hydrothermal conditions, and its structure was determined by X-ray crystallography with the following data： monoclinic, space group C2/c, C12H12N2O8Zn, Mr = 377.61, a = 10.223（3）, b = 10.319（3）, c = 13.613（4）A, β = 105.922（6）°, Z = 4, V = 1380.9（8） A3, F（000） = 768, Dc = 1.816 g/cm3, μ（MoKα ） = 1.826 mm^-1, the final R = 0.0401 and wR = 0.1380 for 1157 observed reflections （I 〉 2σ（I））. In the structure of the title compound, the ZnⅡ ion located in an inversion center lies in a distorted tetrahedral environment at a N2O2 coordination mode, and the 5-hydroxynicotinic acid ligand linkssymmetry-related ZnⅡ ions at aμ2-N,O bridging way forming a two-dimensional covalent structure. In the crystal, solvent water molecules form intermolecular O-H-O hydrogen bonds and pyridine rings of adjacent layers form n-n-stacking （3.346 A）, which connect adjacent two-dimensional sheets into a three-dimensional supramolecular network.

Syntheses,crystal structures,and quantum chemistry calculation of two Ni(Ⅱ)coordination polymers

Two new coordination polymers,[Ni(Hpdc)(bib)(H_(2)O)]_(n)(1)and{[Ni(bib)_(3)](ClO_(4))_(2)}_(n)(2),were prepared by mixing Ni^(2+),3,5⁃pyrazoledicarboxylic acid(H3pdc)/p⁃nitrobenzoic acid and 1,4⁃bis(imidazol⁃1⁃ylmethyl)butane(bib)by a hydrothermal method,respectively.X⁃ray crystallography reveals a 2D network constructed by six⁃coordinated Ni(Ⅱ)centers,bib,and Hpdc2-ligands in complex 1,while a 2D network is built by Ni(Ⅱ)and bib ligands in 2.Furthermore,the quantum⁃chemical calculations have been performed on‘molecular fragments’extracted from the crystal structure of 1 using the PBE0/LANL2DZ method in Gaussian 16 and the VASP program.CCDC:2343794,1;2343798,2.

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.