Two 3D Supramolecular Coordination Polymers Constructed from Aromatic Carboxylic Acids and Flexible Bis(thiabendazole) Ligands

Two coordination polymers (CPs), [Zn(L1)(H₂bta)] (1) and [Co(L2)(ndc)]·0.75H₂O (2), (L1?=?1,6-(thiabendazole)hexane), L2?=?1,3-(thiabendazole)propane, H₄bta?=?1,2,4,5-benzenetetracarboxylic acid, H₂ndc?=?2,6-naphthalenedicarboxylic acid) have been hydrothermally synthesized and characterized. Single crystal X-ray diffraction analyses reveal that CP 1 and CP 2 feature 1D infinite zigzag and “Ω”-like chains, and further extend into 3D supramolecular framework by O–H?O and C–H?O hydrogen bonding interactions, respectively. Furthermore, the luminescence properties, thermal stability, and catalytic degradation of methyl orange in a Fenton-like process are also investigated in detail.     

Two 3D Supramolecular Architectures from Ag(I) Coordination Polymers Constructed by Flexible Bis(benzimidazolyl)butane Ligand

Two Ag(I) coordination polymers, {[Ag(bib)_0.5]Cl·4H₂O} _n (1) with a 1D zigzag chain structure extended into a 3D supramolecular network by face-to-face π–π stacking interactions, and [Ag(bib)(Hpydca)] _n (2) with the first example of three-connected uninodal fourfold interpenetrating ths network via hydrogen-bonding interactions (bib = 1,4-bis(benzimidazole)butane, pydca = pyridine-2,6-dicarboxylate) were synthesized under hydrothermal conditions and characterized by elemental analysis, IR, thermogravimetric analysis and single crystal X-ray diffraction. In addition, the fluorescence properties of 1 and 2 in the solid state were investigated at room temperature.     

Syntheses and Characterization of Three Coordination Polymers of Zinc(II) and Cadmium(II) with Dicarboxylates and Bis(thiabendazole) Ligands

Three d ¹⁰ coordination polymers formulated as [Zn(L1)₂(mip)] _n (1), [Zn(L1)(2,6-ndc)] _n (2) and [Cd(L2)_0.5(bpdc)] _n (3) (L1 = 1,1′-(1,3-propanediyl)bis(thiabendazole), L2 = 1,1′-(1,6-hexanediyl)bis(thiabendazole), H₂mip = 5-methylisophthalic acid, 2,6-H₂ndc = 2,6-naphthalenedicarboxylic acid, H₂bpdc = 4,4′-biphenyldicarboxylic acid) were hydrothermally synthesized. Complexes 1–3 were characterized by elemental analysis, IR spectroscopy, X-ray powder diffraction analysis, and single crystal X-ray diffraction. Complexes 1 and 2 present different chain structures, both of them are extended into 2D supramolecular architectures via C–H···O hydrogen bonds, while 3 is a three-fold interpenetrating three-dimensional framework with binodal 4,4-connected mog topology. The thermal stability, UV–visible spectroscopy and luminescence properties of complexes 1–3 were also examined. Furthermore, complex 3 exhibits relatively positive catalytic activity towards the degradation of methyl orange in a Fenton-like process.     

Synthesis,Structures, and Catalytic Properties of Two Zinc(II) Coordination Polymers Constructed from Polycarboxylate and Bis(Benzimidazole) Ligands

Two Zn(II) coordination polymers, formulated as {[Zn(L1)_0.5(btc)_0.5(H₂O)]·H₂O} _n (1) and {[Zn(L2)(1,4-ndc)]·2H₂O} _n (2) [L1 = 1,4-bis(2-methylbenzimidazole-1-ylmethyl)benzene, L2 = 1,4-bis(2-methylbenzimidazole)butane, H₄btc = butane-1,2,3,4-tetracarboxylic acid, 1,4-H₂ndc = 1,4-naphthalenedicarboxylic acid] have been synthesized and structurally characterized by single crystal X-ray diffraction. Complex 1 features a 3D (3,4)-connected network with the topology of fsh-3,4-P2₁/c. Complex 2 is a 2D (4,4) grid with sql topology and further extends into a 3D supramolecular framework by π–π stacking interactions. In addition, the thermal stability, fluorescence, and catalytic properties of two complexes for degrading methyl orange dye in a Fenton-like process were investigated.     

Synthesis, Crystal Structures and Fluorescence Properties of Two One-Dimensional Cadmium(II) Coordination Polymers Containing Flexible Bis(benzimidazole) Ligands

Two one-dimensional Cd(II) coordination polymers constructed by ribbon-like molecules, {[Cd(L₁)₂(NO₃)]·NO₃} _n (1) (L₁ = 1,3-bis(5,6-dimethylbenzimidazol-1-yl)benzene) and [Cd(L₂)₂(NO₃)₂] _n (2) (L₂ = 1,3-bis(benzimidazol-1-yl)benzene) have been obtained through assembly of the two structurally similar flexible bis(benzimidazole)-based ligands and cadmium nitrate tetrahydrate. The cadmium(II) centers display different coordination environments with trigonal-bipyramidal geometry in 1, and a octahedral geometry in 2. Weak C–H···O interactions in 1 result in a two-dimensional supramolecular layer; two π–π interactions are present in 2 forming a three-dimensional supramolecular network structure. The solid state fluorescence properties of 1 and 2 were investigated.     

Self-Assembly of Polymers through Dynamic Coordination Chemistry and Hydrogen Bonding: Polymers from Mercury(II) Halides and Bis(amidopyridine) Ligands

The synthesis of hybrid organic–inorganic polymers by combination of mercury(II) halides with the ligand 1,5-bis(isonicotinamido)naphthalene, C₁₀H₆(NHCO-4-C₅H₄N)₂, 1. The compounds of formula [HgX₂(1)] form either linear (X = Cl, Br) or zig-zag (X = I) polymers and contain tetrahedral mercury(II) centers with bridging ligands 1. The polymers are further assembled by hydrogen bonding between amide groups. When X = Cl or Br, two-dimensional sheet structures are formed whereas, when X = I, a three-dimensional network is formed. A new polymeric form of [HgCl₂(Me₂SO)] is also described. Dedicated to Ian Manners for his pioneering research on organometallic polymers     

Supramolecular Coordination Polymers by Self-assembling of Bis-monodentate Ligands with HgI2

Two supramolecular coordination polymers, [HgI₂(L¹)·0.5H₂O]_∞ (1) and [HgI₂(L²)·0.4CH₃OH]_∞ (2), have been prepared by ligands L¹ (L¹ = bis[4-(4- pyridylmethyleneamino)phenyl] ether) and L² (L² = N,N′-bis(3-pyridylmethyl)-diphthalic diimide) with HgI₂, respectively. 1 formed an interestingly infinite cross-linked double helical structure, whereas 2 formed the one-dimensional zigzag chains, which are parallel with each other.     

Four Flexible Bis(Thiabendazole)-Based Cd(II) Coordination Polymers with Various Aromatic Carboxylates: Syntheses,Structures and Properties

Four Cd(II) coordination polymers (CPs) including [Cd(btbb)_0.5(L1)] _n (1), [Cd(btbb)(L2)·(H₂O)_1.5] _n (2), [Cd(btbb)(L3)] _n (3), and [Cd(btbb)(HL4)] _n (4) (btbb?=?1,4-bis(thiabendazole)butane, H₂L1?=?5-hydroxyisophthalic acid, H₂L2?=?4,4′-biphenyldicarboxylic acid, H₂L3?=?tetrabromoterephthalic acid, H₃L4?=?5-nitro-1,2,3-benzenetricarboxylic acid) were prepared under hydrothermal conditions based on flexible bis(thiabendazole) ligand and different co-carboxylates. Their structures have been determined by single-crystal X-ray diffraction analyses, elemental analyses, IR spectra, X-ray powder diffraction, and thermogravimetric analyses. CP 1 exhibits a 3D 2-nodal (3,4)-connected framework with the 3,4T10 topology. CP 2 and 3 feature typical hcb layer structure, and 3 is further combined into a 3D supramolecular architecture through C–H?O hydrogen bonds. CP 4 possesses an infinite chain and further extended into 2D supramolecular network by O–H?O hydrogen-bonding interactions. The effects of the aromatic polycarboxylate co-ligands on the CPs framework have been discussed and the catalytic activities of CPs 1–4 for degradation of methyl orange in Fenton-like process are also investigated.     

Supramolecular Design of Coordination Polymers Based on Silver(I) Azide and Nitrogen Donor Ligands

The reactions of K₃[Cu(CN)₄], Me₃SnCl and methylpyrazine (Me-pyz) or tetramethylpyrazine (Me₄-pyz) in water/dioxane system afforded two new coordination polymers (CP); [{Cu(μ-CN)}₂(μ-Me₄-pyz)·dioxane] _n , 1, and [Cu{μ-Mepyz}{μ-CNSn(Me₃)NC–}], 2. X-ray single crystal analysis shows that 1 contains two crystallographically different copper(I) ions which acquire trigonal planar geometry. The structure of 1 contains non-linear (CuCN)_∞ chains that are interconnected by the Me₄-pyz ligands forming 3D-network structure. The structure of 1 has two-fold interpenetrating 3D-networks with dioxane molecules encapsulated in the voids of the structure. The structures of these CP were also investigated by FTIR and mass spectroscopy, thermal analysis and compared with the prototype compounds. Spectroscopic analyses of 2 confirm the presence of all components (Me₃Sn⁺, Cu(CN)₂ ⁻ and Me-pyz) and support the composition predicted by elemental analysis. 1 and 2 display strong fluorescence in the solid state at room temperature.     

Two Energetic Cobalt(II) Coordination Polymers Derived from Isomeric Ligands

Isomer is sometimes fundamental to the formation of the resulting compounds. The design and preparation of coordination compounds based on isomers is of tremendous paramount since they have a lot in common but simultaneously some difference, which can lead to variation of both the topologies and properties. Solvothermal reactions of Hn-pytza (n = 3, 4) with Co(ClO₄)₂·6H₂O, afforded two interesting coordination polymers, one dimensional [Co(3-pytza)₂(H₂O)₂]_n·2nH₂O (1) and three dimensional [Co(4-pytza)₂]_n (2), where Hn-pytza = 5-(n-pyridyl)tetrazole-2-acetic acid (n = 3, 4). The thermal decomposition behavior of the two compounds were characterized by the differential scanning calorimetry (DSC) and thermogravimetric-differential thermogravimetric (TG-DTG), showing [Co(4-pytza)₂]_n is superior to [Co(3-pytza)₂(H₂O)₂]_n·2nH₂O in terms of energetic performance. Furthermore, the entropy of activation (?S), enthalpy of activation (?H), and free energy of activation (?G) were calculated, as well.     

One- and Two-Dimensional Cadmium(II) Tetracyanonickelate(II) Coordination Polymers With Imidazole and 2-Methylimidazole Ligands

Two novel cyano-bridged heteropolynuclear complexes, [Cd(im)₄Ni(μ-CN)₂(CN)₂] _n (1) and [Cd(mim)₂Ni(μ-CN)₄] _n (2) (im: imidazole and mim: 2-methylimidazole), have been synthesized and characterized. In 1, the trans-directed cyanide ligands of [Ni(CN)₄]²⁻ anions link two [Cd(im)₄]²⁺ units, whereas in 2, all the cyanide groups take part in bonding with two adjacent [Cd(mim)₂]²⁺ units, resulting 1D and 2D coordination polymers, respectively. The coordination environment of the Cd(II) ion described as distorted octahedral geometry, whereas around the Ni(II) centre had square planar geometry in both complexes. The crystals packing of 1 and 2 were a composite of hydrogen bonding, π···π and C–H···Ni interactions.     

One-Dimensional Ni(II) and Cu(II) Coordination Polymers Containing Syn-Syn Thiophene-2,5-dicarboxylate and Propane-1,3-diamine

New thiophene-2,5-dicarboxylate complexes with the formula of [M(μ-tdc)(pen)₂] _n (M = Ni(II) (1) and Cu(II) (2), pen = propane-1,3-diamine, tdc = thiophene-2,5-dicarboxylate) have been synthesized and characterized by using thermal (TG/DTG, DTA and MS) analysis, IR and UV–Vis. spectroscopies, magnetic measurement and single crystal X-Ray diffraction techniques. The Ni(II) and Cu(II) ions are distorted octahedrally coordinated by two oxygen atoms of two bridging thiophene-2,5-dicarboxylate ligands and four nitrogen atoms of the trans-pen ligands. The polymeric chains are connected together by hydrogen bonds interactions, forming three-dimensional network.     

Hydrothermal Synthesis, Crystal Structures and Fluorescent Properties of Two New d10 Metal Coordination Polymers with Two Mixed Flexible Ligands

Two complexes, [Zn(qda)(bpp)] _n (1) and {[Cd(qda)(bpp)₂]·2H₂O} _n (2), (H₂qda?=?hydroquinone-O,O′-diacetic acid, bpp?=?1,3-bis(4-pyridyl)propane), were hydrothermally synthesized and characterized by single crystal X-ray diffraction analysis, FTIR and elemental analysis. Both compounds exhibit two-dimensional structures. The qda anions in compound 1 adopt two different trans conformations, coordinating to Zn²⁺ ions in a monodentate fashion, while in compound 2 they adopt only one trans conformation yet keeping the same coordination fashion as in compound 1. The bpp molecules show same anti-gauche coordination conformation in both 1 and 2. In addition, photoluminescence for 1 and 2 has been investigated in the solid state at room temperature.     

Synthesis,Characterization, and Magnetic Properties of Two Transition Metal Coordination Polymers Based on 2,5-Furandicarboxylic Acid and N-Donor Ligands

Two new transition metal-based coordination polymers, [Cu(fdc)(dmbpy)(H₂O)]_n (1) {[Ni₂(fdc)₂(bipy)₂(H₂O)₄]·(H₂O)₂}_n (2) (fdca = 2,5-furandicarboxylic acid, dmbpy = 3,3′-dimethyl-4,4′-bipyridine, bipy = 4,4′-bipyridine) have been synthesized under the same reaction conditions (H₂O, pH 7–8, and 130 °C) and were structurally characterized. 1 is a ladder chain, whereas 2 shows a 2D (4,4) network. Both 1 and 2 are further connected into 3D structures through hydrogen bonds. Furthermore, the magnetic properties of 1 and 2 are also investigated.