Syntheses,Structures and Properties of Three Novel La(Ⅲ)/Co(Ⅱ) Coordination Polymers Based on 5-(3-(Tetrazo-5-yl)phenyl)isophthalic Acid

Three novel complexes, namely {[La(tapipa)(4,4′-bibp)·(H_2O)_2]·H_2O}n(1), {[La-(tapipa)(H_2O)_4(OH)]·3 H_2O}n(2), [Co(tapipa)(1,4-bbib)]n(3)(tapipa = 5-(3-(tetrazo-5-yl)phenyl)isophthalic acid, 4,4′-bibp = 4,4′-bis(imidazolyl)biphenyl, and 1,4-bbib = 1,4-bis(benzimidazo-1-ly)benzene) have been synthesized under solvothermal conditions and characterized by PXRD, IR,TGA, and so on. Complex 1 presents a 2 D layer structure, which is finally packed into a 3 D supramolecular structure by means of hydrogen bonds; complexes 2 and 3 exhibit 1 D chains and 2 D wavy-type structures, respectively, which are expanded into 3 D supramolecular structures through hydrogen bonds and π-π interactions. Furthermore, the luminescence properties of complex 1 and the variable-temperature magnetic susceptibilities of 3 were investigated. Complex 1 has highly selective sensing for Fe~(3+) and Cr_2O_7~(2-) ions.     

Synthesis,Structure, and Luminescent Properties of Two Complexes Based on Flexible Phenylenediacetate Ligand

Two new Zn(Ⅱ) and Cd(Ⅱ) coordination complexes, [Zn(ppda)(idz)]_n(1) and [Cd(mpda)(mbib)]_n(2)(H2 ppda = 1,4-phenylenediacetic acid, H_2 mpda = 1,3-phenylenediacetic acid, idz = imidazole, mbib = 1,3-bis(imidazol-1-ylmethyl)benzene), have been synthesized by using Zn(Ⅱ)/Cd(Ⅱ) salt and phenylenediacetic acid in the presence of different imidazole ligands under hydrothermal conditions, and characterized by elemental analysis, IR spectroscopy, single-crystal X-ray crystallography and thermogravimetric analysis. Complex 1 crystallizes in orthorhombic system, Iba2 space group. The carboxylic acid ligands form a 2 D helical layer with Zn(Ⅱ) ions, and such layers are expanded into a 3 D network structure by the force of C–H×××π. Complex 2 crystallizes in monoclinic system, P2_1/n space group. Complex 2 shows a 3 D framework with two Cd(Ⅱ) ions as nodes of a dual-core unit, which can be considered to be 6-connected net and regarded as a rare(4~4,5~(10),7) topology network with self-interlacing. The structural diversities indicate that rigid and flexible imidazole ligands play dominating roles in modulating the formation of structures of these crystalline materials. Moreover, the luminescent properties of two complexes are investigated in solid state.     

Syntheses,Crystal Structures,and Magnetic Properties of Cobalt(Ⅱ) Complexes with 1,1-Cyclohexanediacetic Acid

Two new Co(Ⅱ) coordination polymers,{[Co_3(Hchda)_2(chda)_2(bpp)_2(H_2O)_2]}_n 1 and {[Co(chda)(bpe)(H_2O)]·3H_2O}_n 2(H_2chda = 1,1-cyclohexanediacetic acid,bpp = 1,3-bis(4-pyridinyl)propane and bpe = 1,2-bis(4-pyridinyl)ethylene),were hydrothermally synthesized and then characterized by elemental analysis,IR spectroscopy,thermogravimetric analysis(TGA),and single-crystal X-ray diffraction.Complex 1 possesses an infinite metal-organic layer based on triply bridged linear trinuclear subunits and complex 2 exhibits a square(4,4) grid layer with dangling lateral arms resulting from eight-membered rings above and below the layer.In addition,magnetic properties of complexes 1 and 2 are also given.     

Syntheses,Structures, and Properties of Two Cobalt(Ⅱ) Coordination Complexes Based on(Fluorene-9,9-diyl) dipropanoic Acid and 1,3-Bis(imidazol-1-yl)butane Ligands

Two new cobalt(II) coordination complexes, namely [Co(HL)_2(biim)(H_2O)_2]_n·n H_2O(1) and [Co(Et L)_2(biim)]_n·3 n(H_2O)·2 n(Et HL)(2)(H_2L =(fluorene-9,9-diyl)dipropanoic acid, biim = 1,3-bis(imidazol-1-yl)butane), have been synthesized using the same starting reactants but different solvent medium. The two complexes exhibit distinctly different structures. Compound 1 exhibits a one-dimensional linear chain structure. However, complex 2 reveals a one-dimensional zigzag chain structure. Thermogravimetric analyses(TGA) and luminescent properties of these two complexes have been discussed.     

Fluorescence Properties and Crystal Structures of Metal-organic Coordination Complexes Based on the 2,6-Naphthalenedicarboxylic Acid

Two metal-organic coordination complexes, [Zn(2,6-ndc)(1,2-bix)]_n(1) and [Zn(2,6-ndc)(1,3-bix)]n(2)(2,6-H_2ndc = 2,6-naphthalenedicarboxylic acid, 1,2-bix = 1,2-bis(imidazole-1-ylmethyl)-benzene and 1,3-bix = 1,3-bis(imidazole-1-ylmethyl)-benzene) have been synthesized by the hydrothermal method. Though the two complexes both crystallize in a triclinic system, space group P1 and show similar two-dimensional structures, weak intermolecular interactions(π-π packing interactions) only exist in complex 2. They are characterized by single-crystal X-ray diffraction analysis, fluorescence measurement, IR spectroscopy and TGA. Moreover, the solid-state fluorescence spectra of two complexes show maximal emission peaks at 365(λ_(ex) = 329 nm) and 367 nm(λex = 344 nm), respectively.     

Syntheses and Characterizations of Two Manganese(Ⅱ) Coordination Polymers Containing Three-dimensional Interpenetrating Networks Constructed by Mixed Ligands

Two new three-dimensional coordination polymers, namely [Mn(L)(bpdc)]n(1), [Mn(L)0.5(ndc)]n(2)(L = 1,4-bis(2-methylbenzimidazole)butane, H2 bpdc = 4,4?-biphenyldicarboxylic acid, H2 ndc = 2,6-naphthalenedicarboxylic acid) have been successfully synthesized under hydrothermal conditions. Two complexes were characterized by physico-chemical, spectroscopic methods and single-crystal X-ray diffraction. Complex 1 shows a 3D → 3D 5-fold interpenetrated network with a 4-connected uninodal dia topology. Complex 2 possesses a 3D → 3D 3-fold interpenetrating architecture with a binodal(4,5)-connected xah topology. The fluorescence and thermal properties of the title complexes were discussed.     

Syntheses,Structures and Characteristics of Two New Cu(Ⅱ) Coordination Polymers Based on 4-tert-butyl-phthalate and Different Bis(1,2,4-triazol-1-yl) Co-Ligands

Two new Cu(II) coordination polymers, [Cu2(tbph)2(btb)2]n(1) and {[Cu2(tbph)2-(bth)2]·H2O}n(2),(H2tbph = 4-tert-butyl-phthalic acid, btb = 1,4-bis(1,2,4-triazol-1- yl)butane, bth = 1,6-bis(1,2,4-triazol-1-yl)hexane), have been synthesized and characterized by elemental analysis, FT-IR and X-ray single-crystal diffraction. Complex 1 has a 2D sql layer. Complex 2 shows a(3,4)-connected 2D sheet with a(4.64.8)(4.82) topology. The thermal behavior of the two corresponding complexes has briefly been investigated.     

Two Zn~Ⅱ Coordination Polymers with 2,2?-Oxybis(benzoic acid) and Different N,N?-Donor ligands

Two new Zn~Ⅱ coordination polymers [Zn(oba)(4,4?-bipy)]n(1) and [Zn(oba)-(bpe)_(1/2)(H_2O)]_n(2)(H_2oba = 2,2?-oxybis(benzoic acid), 4,4?-bipy = 4,4?-bipyridine, bpe = 1,2-bis(4-pyridyl)ethylene) were synthesized by hydrothermal reactions and characterized by single-crystal X-ray diffraction, thermogravimetric analysis, IR spectroscopy and elemental analysis. Complex 1 shows a 3D metal-organic framework with a uninodal 4-connected 65.8 dmp network. Complex 2 features 1D ladder-shaped chains, which are further connected into a 2D stair-step network through intermolecular O–H···O hydrogen bonds.     

Two Metal-organic Coordination Polymers with Rigid Bis(triazole) Ligand: Assembly,Structures, and Fluorescence Properties

Two new coordination polymers containing rigid bis(triazole), namely, [Ni(btb)_(0.5)(nph)(H_2O)]_n(1) and [Zn(btb)(SO_4)]_n(2)(btb = 4,4?-bis(1,2,4-triazolyl-1-yl)-biphenyl, H_2nph = 3-nitrophthalic acid) have been synthesized and characterized by elemental analysis, IR spectra, and single-crystal X-ray diffraction. Complex 1 shows a 3D trinodal(3,4,4)-connected sqc69 topology. Complex 2 presents a 2D uninodal 4-connected sql network, which is further packed into a 3D supramolecular framework by C–H···O hydrogen bonds. Thermal stabilities and fluorescence properties of two complexes have been discussed in detail.     

Syntheses,Structures,and Photoluminescent Properties of Two Zn(Ⅱ) Coordination Polymers with Helical Chains Structures

Two novel coordination polymers with helical chains, {[Zn(L)(H2O)]?H2O}n(1) and {[Zn(L)(p-bix)]?3.5H2O}n(2), where H2 L = 5-(4-hydroxypyridinium-1-ylmethyl) isophthalic acid and p-bix = 1,4-bis(imidazol-1-ylmethyl)benzene, have been hydrothermally synthesized, and charac-terized by elemental analysis, powder X-ray diffraction(PXRD), IR, thermal gravimetric analyses(TGA) and also by single-crystal X-ray diffraction. Both complexes 1 and 2 crystallize inmonoclinic, space group P21/c. Compound 1 displays a two-dimensional(2D) structure with two distinct types of helical chains; 2 shows a layered coordination polymer with two types of helical chains and features an interesting 2D→3D interdigitated architecture. Meanwhile, the luminescent properties of 1 and 2 have also been investigated in detail.     

Two Co(Ⅱ) Complexes Constructed from 1-(3,5-Dicarboxybenzyl)-3,5-pyrazole Dicarboxylic Acid:Syntheses,Structures and Magnetic Properties

Two new complexes[Co_2(L)(4,4′-bip)(H_2O)_3]_n (1) and{[Co(L′)_2(phen)]·2H_2O)}_n (2)(H_4L=1-(3,5-dicarboxybenzyl)-3,5-pyrazole dicarboxylic acid,H_3L′=1-(3,5-dicarboxybenzyl)-3-pyrazole carboxylic acid,4,4′-bip=4,4′-bis(1-imidazolyl)biphenyl,phen=1,10-phenanthroline) were synthesized.Complexes 1 and 2have been characterized by IR spectrography,X-ray single-crystal diffraction,elemental analysis and thermogravimetry.1 crystallizes in monoclinic system,space group P2_1/c.Complex 2 crystallizes in monoclinic system,space group I2/a.It is remarkable that in situ hydrothermal decarboxylation was observed during preparing complex 2.In addition,magnetic analysis indicates that antiferromagnetic interaction exists among Co(Ⅱ) ions in complexes 1 and 2.     

Three Novel Luminescent Zinc(Ⅱ) Compounds Constructed by Employing Mixed-ligand Strategy

Three novel coordination polymers,[Zn(suc)(o-bix)]_n (1),[Zn(suc)(m-bix)·H_2O]_n (2) and[Zn_2(suc)_2(p-bix)_2·4H_2O]_n (3)(H_2suc=succinic acid,o-bix=1,2-bis(imidazol-1-ylmethyl)-benzene,m-bix=1,3-bis(imidazol-1-ylmethyl)-benzene,p-bix=1,4-bis(imidazol-1-ylmethyl)-benzene),have been synthesized and structurally characterized by elemental analysis,IR spectroscopy,thermogravimetric analysis,powder X-ray diffraction,and single-crystal X-ray diffraction.These three coordination polymers present various structures originated from auxiliary N-donor ligands with different configurations.Compound 1 shows a 2D network with4~4-sql topology.Compound 2 exhibits an infinite chain,and the adjacent chains are extended into a 2D sheet byπ-πstacking interactions.Changing the conformation of the N-donor ligand leads to 3 featuring a 3D framework with a novel 4-connected (6~5·8) topology.In addition,the solid-state photoluminescent properties of compounds 1～3 are investigated.     

Spacer Length Effects on the Structure of Cd(Ⅱ) Coordination Polymers with Flexible Bis(thiabendazolyl)(1) Alkane and 1,2,4,5-Benzenetetracarboxylte Ligands

The hydrothermal reactions of Cd(OAc)2·2H2O with 1,2,4,5-benzenetetracarboxylic acid(H4bta) and 1,4-bis(thiabendazolyl)butane(L1) or 1,6-bis(thiabendazolyl)hexane(L2) afforded two coordination polymers [Cd2(L1)(bta)·2H2O]n(1) and [Cd2(L2)2(H2bta)2]n(2). Complex 1 holds a rare 3D binodal(4,6)-connected framework with fsh topology. Complex 2 features an infinite meandering chain structure, which is further extended via O–H···O hydrogen bonding into a 3D supramolecular network. The thermal and fluorescence proprieties of the two complexes were investigated.     

Solvothermal Syntheses,Crystal Structures,and Luminescent Properties of Three Coordination Polymers Derived from Semirigid 3-(Carboxymethyl)benzonic Acid and Dipyridyl Coligands

Three coordination polymers, namely, {[Zn(cmba)(bpp)]×H_2O}_n(1), {[Zn(cmba)(bpa)1.5]×2.25H_2O}_n(2) and {[Cd(cmba)(bpa)(H_2O)]×H_2O}_n(3)(H_2cmba = 3-(carboxymethyl)benzonic acid, bpp = 1,3-bis(4-pyridyl)propane and bpa = 1,2-bi(4-pyridyl)ethane), were synthesized under solvothermal conditions and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis(TGA), and single-crystal X-ray diffraction. Complex 1 features a 2D(4,4) grid layer with a side length of 9.827(10)/12.176(13) ?. Complex 2 shows a 2D → 2D 2-fold interpenetrating layer structure through the flexible bpa coligands. Compound 3 presents a 2D layer formed from the metal-carboxylate chains further extending through bpa pairs. Furthermore, the solid state luminescent properties of complexes 1~3 were investigated at room temperature.     

Two Interpenetrated and Polycatenated Zn(Ⅱ) Coordination Polymers: Syntheses,Structures and Luminescent Properties

Two fascinating Zn(II)entangled coordination polymers,[Zn(eoba)(bbi)]_n·nH_2O(1)and[Zn(boba)(bbi)_(1/2)]_n(2),(bbi=1,1?-(1,4-butanediyl)-bis(imidazole),H_2eoba=4,4?-(ethane-1,2-diyldioxy)-dibenzoic acid,H_2boba=4,4?-(butane-1,4-diyldioxy)-dibenzoic acid),were obtained by hydrothermal technology and characterized by elemental analysis,infrared spectrum,thermogravimetric analysis and single-crystal X-ray diffraction.1 is a rare 2D→3D example with a 3-fold parallel interpenetration and polycatenaned architecture.2 features a scarce2D→2D example with a 3-fold parallel interpenetrating network which possesses polyrotaxane and polycatenane characters.Moreover,the luminescent properties of 1 and 2 have been discussed.     

Coordination Assemblies of Cd~(Ⅱ) with 5-(Ethylthio)-1H-tetrazole and Halide Ions: Synthesis,Structure, and Luminescent Properties

Three cadmium(II)-halide complexes with 5-(ethylthio)-1H-tetrazole(Hett) as ligand, namely [Cd_7Cl_2(ett)_(12)(H_2O)_2]_n(1), [Cd_2(OH)Br(ett)_2]_n(2) and [Cd_2(OH)I(ett)_2]_n(3), have been hydrothermally synthesized and characterized. Complex 1 was synthesized at pH = 7 and exhibits a 3D supramolecular framework, where the adjacent Cd ions form a tetrahedron unit by ett ligands bridge and the tetrahedron units share vertices to connect each other by ett bridges to form a 2D layer architecture, which is further interlinked by μ_2-Cl to form 3D structures. Complexes 2 and 3 are isostructural, generated at pH = 8.0~9.0, displaying similar 2D networks via ett ligands and different halide ions(Br-in 2, I-in 3, respectively). In addition, thermal stabilities and luminescent properties of new complexes 1~3 have been studied.     

Synthesis and Crystal Structure of a New Zinc(Ⅱ) Coordination Polymer Assembled by 4-Nitrophthalic Acid and Bis(imidazol) Ligands

A new complex [Zn(4-nph)(bib)]_(2n)·nH_2O(1) has been obtained by the reaction of metal(Zn(Ⅱ)),1,4-bis(imidazol-1-yl)-butane(bib) with 4-nitrophthalic acid(4-H_(2nph)).The crystal structure of 1 has been determined by single-crystal X-ray diffraction analysis.Compound 1 is of triclinic system,space group P1 with a = 10.3251,b = 12.4503,c = 16.6497 ?,α = 88.487(3),β = 72.529(3),γ = 79.991(3)°,V = 2009.8(5) ?~3 and Mr = 945.47.Complex 1 shows a three-dimensional(3 D) framework.Moreover,through intermolecular hydrogen bonds,compound 1 is assembled into a supramolecular structure.The thermal stability and luminescent properties of 1 are also investigated.     

Synthesis,Structure and Slow Magnetization Relaxation of Co(Ⅱ) Complexes from a Flexible Imidazole-based Ligand

The employment of a flexible imidazole-based ligand(H_2L), condensed from 1 Himidazole-2-carbaldehyde and 1,2-bis(aminooxy)ethane, and Co~(2+) salt has led to the formation of Co(Ⅱ) complexes [Co(H_2L)_2Cl]Cl·4CH_3OH(1) and [Co(H_2L)(NCS)_2]_2·2C_4H_(10)O(2), in the presence of different anions, i.e, Cl-and SCN-, respectively. Single-crystal X-ray analyses show that complex 1 with a square pyramid(C_(4v)) local environment exhibits a two-dimensional(2D)layered(4,4)-net framework and complex 2 displays a dinuclear molecule box with a T_d local environment. By comparison between complexes 1 and 2, the versatile configuration of ligand including cis-and trans-form isomer has a significant effect on the structures of the resulting complexes. The magnetic properties of 1 and 2 are also investigated. The ac magnetic susceptibility revealed that 2 exhibits the characteristic of slow magnetization relaxation.     

Auxiliary Ligand Oriented Cd~(Ⅱ)-flexible Dicarboxylic Acid Coordination Frameworks:Syntheses,Structures and Properties

Two different Cd~(Ⅱ) coordination frameworks [Cd(L1)(L2)]_∞(1) and [Cd(L1)-(L3)(H_2O)]_∞(2) based on a flexible dicarboxylic acid ligand were obtained by introducing two different nitrogen heterocyclic auxiliary ligands(L1 = 3,3'-[1,3-benzenebis(carbonylimino)]bi(benzoate), L2 = 1,3-bi(4-pyridyl)propane, L3 = 4,4'-bipyridine). Complex 1 crystallizes in triclinic, space group P■ with a = 8.7415(5), b = 12.2247(7), c =16.2415(10) ?, β = 95.6790(10)°, V = 1525.11(16) ?~3, D_c = 1.553 mg·m~(-3), C_(35)H_(28)CdN_4O_6, M_r = 713.02, F(000) = 724, μ(MoKα) = 0.770 mm~(–1), Z = 2, R/wR(I 2σ(I))~a = 0.0302/0.0773. However, complex 2 crystallizes in monoclinic, space group P2_(1/n) with a = 11.4986(7), b = 23.0911(14), c = 11.9943(8) ?, β = 115.9500(10)°, V = 2863.6(3) ?~3, D_c = 1.598 mg·m~(-3), C_(32)H_(24)CdN_4O_7, M_r = 688.96, F(000) = 1392, μ(MoKα) = 0.820 mm~(–1), Z = 4, R/wR(I 2σ(I))~a = 0.0283/0.0631. The structures of two complexes were characterized. Complexes 1 and 2 have different one-dimensional(1D) chain structures. In addition, we have also made a preliminary study on the properties of the two complexes.     

Structures and Photoluminescent Properties of Two Complexes Based on Dipyrido[3,2-a:2?,3?-c]phenazine and 2,4?-Biphenyldicarboxylic Acid

ABSTRAC Two new complexes [Cd(2,4?-bpdc)(DPPZ)]_(2n)·n H_2O(1) and [Zn(2,4?-Hbpdc)_2(DPPZ)]· H_2O(DPPZ = dipyrido[3,2-a:2?,3?-c]phenazine, 2,4?-H_2bpdc = 2,4?-biphenyldicarboxylic acid) have been hydrothermally synthesized. The structure of complex 1 was determined by single-crystal X-ray diffraction diffraction and further characterized by elemental analysis, IR spectrum, powder X-ray diffraction(XRD) and single-crystal X-ray diffraction. Complex 1 has 1D chains, which are further connected by π-π stacking interactions of neighbouring chains, generating a steady 3D supramolecular structure. Complex 2 shows the isolated mononuclear units, which are further extended to a 2D supramolecular layered structure through π-π stacking interactions and hydrogen bonds. Furthermore, complexes 1 and 2 exhibit green photoluminescent properties at room temperature.