Hydrothermal Syntheses and Crystal Structures of Two Coordination Polymers with Terephthalic Acid and N-Donor Ligand: 2-Methyldipyrido[3,2-f:2′,3′-h]quinoxaline

Two 3D coordination polymers, [Cd(BDC)(Medpq)·H₂O]_n 1, and [Co(BDC)(Medpq)·H₂O] _n 2 (BDC = terephthalic acid, Medpq = 2-Methyldipyrido[3,2-f:2′,3′-h]quinoxaline), have been synthesized by self-assembly. The structure analyses show that both of the two coordination polymers are formed by 1D infinite chains through non-covalent interactions, and both of them are based on 1D zigzag ones. The photoluminescent study of the coordination polymer [Cd(BDC)(Medpq)·H₂O] _n shows that it exhibit fluorescent emission bands at 567.7 nm.     

Synthesis, Structures and Luminescent Properties of Two New Cd(II) Coordination Polymers Based on V-Shaped 3,3′,4,4′-Oxidiphthalic Acid

Two new Cd(II) coordination polymers, namely [Cd₂(H₂OA)₂(μ₂-H₂O)(H₂O)₆] _n ·3nH₂O (1) and [Cd₂(H₂OA)(phen)₂] _n ·nH₂O (2) (H₄OA = 3,3′,4,4′-oxidiphthalic acid, phen = 1,10-phenanthroline) have been synthesized by combining H₄OA or H₄OA and phen with Cd(II) salts under hydrothermal conditions. Single-crystal X-ray diffraction analysis reveals that 1 features a hydrogen-bond directed two-dimensional (2D) layered structure constructed from alternating left- and right-handed double strand helical chains, 2 represents a one-dimensional (1D) chain structure with the phen molecules dangling on it, which is further extended into a three-dimensional (3D) supramolecular framework through strong face-to-face π···π interactions. In addition, luminescent properties of these two compounds were also investigated in the solid state at room temperature.     

Syntheses, Structures and Properties of Two Metal–Iodide Polymers Based on a Flexile N-Donor Ligand

Two novel metal–organic frameworks based on 1,3-bis(imidazol-1-ylmethyl)-benzene (m-bix), namely [(Cu₄I₄)(bix)₂] _n (1) and [HgI₂(bix)] _n (2) have been synthesized and characterized by IR, elemental analysis, thermogravimetry, luminescent properties and X-ray crystallography. The structure of compound 1 exhibits a 1D metal–organic chain composed of Cu₄I₄ clusters and m-bix ligands, and such chains are further united together to generate a 3D supramolecular structure through inter-chain π···π interactions. In compound 2, the HgI₂-bix chains interact each other to form a layer structure through π···π interactions, then the layers are extended to 3D supramolecular architecture through intermolecular C–H···π interactions.     

Syntheses,Crystal Structures and Properties of Two Supramolecular Coordination Polymers with 2,6-Pyridinedicarboxylic Acids and 4,4′-Bis(imidazolyl)biphenyl

Two supramolecular coordination polymers, [Cu(PDA)(4,4′-bibp)]_n (1) and [Zn(PDA)(4,4′-bibp)]_n (2) (PDA = 2,6-pyridinedicarboxylic acid and 4,4′-bibp = 4,4′-bis(imidazolyl)biphenyl), have been obtained under hydrothermal conditions. The two polymers were characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction analysis. The X-ray single crystal analysis revealed that two complexes exhibit different supramolecular architectures. The photocatalytic studies indicate complex 1 is a good candidate for the photocatalytic degradation of methylene blue, rhodamine B and methylene violet. The photoluminescence behaviour of complex 2 was also discussed.     

Synthesis, Structure and Luminescence Property of Cadmium(II) Coordination Polymer with Mixed 5-(Oxidediphenylphosphino)isophthalic Acid and 4,4′-Bipyridine Ligands

A new metal–organic framework {[Cd(L)(4,4′-bpy)]₂·5H₂O} _n (1) had been synthesized by hydrothermal reaction of 5-(oxidediphenylphosphino)isophthalic acid, Cd(II) nitrate, NaOH and 4,4′-bipyridine (4,4′-bpy) as co-ligand. The novel compound was characterized by single crystal X-ray diffractometry as well as FTIR spectrum. Adjacent eight-member (C₂Cd₂O₄) rings are connected each other through pairs of L^2? ligands to result in a 1D double chain. Such ribbons are interconnected together by 4,4′-bpy to generate a 2D pillared layer, which are further held together by rich O–H···O hydrogen bonds to give a 3D supramolecular network. Solvent water molecules play an important role to bridge adjacent layers to form a 3D supramolecular architecture. The luminescence property and thermogravimetric analysis of title complex were investigated.     

Syntheses and Characterization of New Nano-porous Soft Copper(II) Metal–organic Framework and Nano-porous Two-dimensional Manganese(II) and Zinc(II) Coordination Polymers with 4,4′-Bipyridine and 2-Sulfobenzoic Acid

Three new Cu(II), Mn(II), and Zn(II) coordination polymers with 4,4′-bipyridine (4,4′-bipy) and 2-sulfobenzoic acid (2-H₂sb) ligands, [M(4,4′-bipy)(2-sb)(H₂O)]_n, have been synthesized and characterized by IR spectroscopy and elemental analyses. The structures were determined by single-crystal X-ray crystallography. The structural studies show that the metal atoms have six-coordinate geometry with a distorted octahedral environment constructed with 4,4′-bipy and 2-sb²⁻ linkers stacked over each other to generate a two-dimension motif. Self-assembly of these compounds in the solid state is likely caused by coordination and hydrogen-bonds. While polymers containing Zn(II) and Mn(II) have analogous structures, the Cu(II)-containing nano-porous soft metal–organic framework presents a different structure.     

Dimethyltin(IV) Coordination Polymers Featuring the Versatile Ligand of 2,2′-Bipyrimidine: A Multi-NMR,Hirshfeld Surface Analysis Study and Thermal Properties

Journal of Inorganic and Organometallic Polymers and Materials - Dimethyltin(IV) complex SnMe2(NCS)2 form two coordination polymers when react with the tetradentate 2,2′-bipyrimidine (bpym)...     

Synthesis and Self-assembling Properties of 2,2′:6′,2″-Terpyridine-Based Carbon Nanotube Coordination Polymers

A novel metallo-supramolecular polytopic ligand was synthesized from the attachment reaction involving an amino group-functionalized multi-wall carbon nanotube and 4-chloro-2,2′:6′,2″-terpyridine used for the preparation of metallo-supramolecular polymers with Co(II) or Ni(II) ions. Different colors were observed depending on either the ligands or the metal ions in this type of supramolecular assembly. The created supramolecular polymers were characterized by means of structure, morphology, and stimuli-responsive performance employing scanning electron microscopy, amperometric techniques, UV–Vis and Fourier transform infrared spectroscopy. UV–Vis spectroscopy and cyclic voltammetry studies confirmed that both the optical and electrochemical properties of metallo-supramolecular materials are affected by the substituent at the pyridine periphery.     

Pervaporation of water/acetic acid through polyimide membranes from 3,3′, 4,4′-benzophenone tetracarboxylic dianhydride and 4,4′-oxydianiline

Summary Pervaporation performance of polyimide (PI) membrane from 3,3, 4,4-benzophenone tetracarboxylic dianhydride (BTDA) and 4,4-oxydianiline (ODA) was investigated at 80wt% feed acetic acid concentration and at 65°C. Imide contents in PI film were estimated by thermogravimetric analysis (TGA) method. The separation factor of PI membrane increases with the degree of imidization, while the flux was almost constant. The separation factor toward water through PI-94 membrane was about 417 with the flux of 47 g/m². hr measured at 65°C and with 80wt% acetic acid as a feed. PI-94 showed the best pervaporation performance toward the separation of water from acetic acid solution among the PI membranes investigated. The swelling behaviors at various feed concenration were also examined.     

Synthesis and Structural Characterization of Triorganotin(IV) Derivatives with 2,2′-Thiodiglycolic Acid and 3,3′-Thiodipropionic Acid

The synthesis and structural characterization of four novel triorganotin(IV) complexes, {(R₃Sn)₂[C₂H₄S(COO)₂]} _n (R = Me: 1), {(R₃Sn)₄[C₂H₄S(COO)₂]₂} _n (R = nBu: 2), {(R₃Sn)₂[C₄H₈S(COO)₂]} _n (R = Me: 3; nBu: 4) were obtained by the reaction of 2,2′-thiodiglycolic acid, 3,3′-thiodipropionic acid and the corresponding R₃SnCl (R = Me, nBu) with potassium hydroxide in methanol. All the complexes were characterized by elemental analysis, Fourier transform infrared and nuclear magnetic resonance (¹H, ¹³C, ¹¹⁹Sn) spectroscopies, X-ray crystallography and thermogravimetric analyses. The crystal structures show that 1 has 2D network structure in which 2,2′-thiodiglycolic acid acts as a tetradentate ligand coordinating to the trimethyltin(IV) ions. Complexes 2, 3, and 4 are 3D metal-organic framework structures in which the deprotoned acids act as a tetradentate ligand afforded by four oxygen atoms.     

Syntheses, Crystal Structures, Thermal Stabilities and Luminescent Properties of Two Pillared Layered Alkaline–Earth Coordination Polymers

Two new three-dimensional pillared layered coordination polymers, [M(2,5-PDC)H₂O]_n [M(II) = Sr(1), Ba (2)] were synthesized under hydrothermal conditions using alkaline–earth metal centers strontium and barium with 2,5-pyridinedicarboxylic acid as the organic ligand. The structures of two compounds have been determined by single-crystal X-ray diffraction analyses and further characterized by IR spectrum, elemental analyses, powder X-ray diffraction, and thermogravimetric analyses. The compounds are isostructural, confirmed by their powder XRD measurements. They feature a pillared layered framework structures. Within the layer, the dinuclear [M₂O₂] units through the bridge of the coordination water molecule are found, which are connected by carboxylate groups along the a- and b-axis, respectively. The layers are further pillared by the pyridyl groups of the 2,5-PDC^2? ligands. Furthermore, the luminescent properties of two compounds have also been investigated in the solid state.     

A 3D Mesomeric Supramolecular Structure of a Cu(II) Coordination Polymer with 1,1′-Biphenyl-2,2′,3,3′-tetracarboxylic Acid and 5,5′-Dimethyl-2,2′-bipyridine Ligands

A novel metal–organic framework {[Cu(H₂bptc)(cbpy)(H₂O)]·(H₂O)} _n (1) has been hydrothermally synthesized through reaction of 1,1′-biphenyl-2,2′,3,3′-tetracarboxylic acid (H₄bptc) with Cu(II) salt in the presence of ancillary nitrogen ligand 5,5′-dimethyl-2,2′-bipyridine (cbpy), and its structure was determined by X-ray diffraction and characterized by elemental analysis, and IR spectrum. The title compound crystallizes in monoclinic space group P2₁/c. Both right- and left-handed helices are detected in the structure. In the ab-plane, adjacent chains are homochiral and parallel to each other, which are connected together by hydrogen bonds to form a 2D supramolecular structure. The supramolecular layers with opposite chirality are arranged alternatively along the c-axis to form a 3D mesomeric supramolecular structure through π···π interactions. The thermal stability of the complex 1 was studied by thermal gravimetric and differential thermal analysis.     

Syntheses and Characterization of Two New M(II)-5,5′-dimethyl-2,2′-bipyridine (M = Cd and Pb) Coordination Polymers and Study of Their Thermal and Electrochemical Properties

Two new cadmium(II) and lead(II)-thiocyanato coordination polymers with 5,5′-dimethyl-2,2′-bipyridine (5,5′-dm-2,2′-bpy) as chelating ligands were synthesized and characterized by elemental analysis, IR and ¹H NMR spectroscopy and by X-ray crystallography. Thermal and electrochemical properties were also studied as well. These complexes have formed formula [Cd(5,5′-dm-2,2′-bpy)(NCS)₂]_n (1) and [Pb(5,5′-dm-2,2′-bpy)(CH₃COO)(NCS)]_n (2). The coordination numbers of Cd^II in 1 and Pb^II in 2 are six (CdN₄S₂) and seven (PbN₃O₃S₂), respectively. In 2, “stereo-chemically active” electron lone pairs and the coordination spheres were hemidirected. Bridging properties of thiocyanato anions in 1 and 2 created one- and two-dimensional coordination polymers, respectively. The supramolecular features in these complexes were guided and controlled by weak directional intermolecular interactions.     

Synthesis,characterization and crystal structure of one Mn(II) complex with 4,4′-bisimidazolylbiphenyl and 4,4′-sulfonyldibenzoic acid

One new title compound [Mn₃(BIBP)(sdb)(NO₂⁻)₂(H₂O)₂]_n·2DMF (1) (BIBP = 4,4′-bisimidazolylbiphenyl, sdb = 4,4′-sulfonyldibenzoic acid) has been synthesized under hydrothermal condition. The title compound was characterized by IR spectra, thermal analysis, single crystal and powder X-ray diffraction. Magnetic susceptibility measurements indicate that compound 1 exhibits antiferromagnetic coupling interaction.     

Hydrothermal Synthesis of Metal–Organic Coordination Polymers Constructed from Asymmetric Semi-rigid V-shaped Dicarboxylate and Nitrogen-Contained Mixed Ligands

Three new coordination polymers, [Ni(2,4′-oba)(1,10-phen)] _n (1), {[Ni (2,4′-Hoba)₂(4,4′-bipy)(H₂O)₂]·2H₂O} _n (2) and [Zn(2,4′-oba) (4,4′-bipy)] _n (3) (2,4′-H₂oba = 2-(4-carboxyphenoxy)benzoic acid, 1,10- phen = 1,10-phenanthroline, and 4,4′-bipy = 4,4′-bipyridine) have been obtained by hydrothermal synthesis. The framework structures of these polymeric complexes have been determined by single-crystal X-ray diffraction studies. Complex 1 exhibits double-helical chains formed by π–π stacking interactions from the phenyl rings of the 1,10-phen ligands. Complex 2 forms a two-dimensional supramolecular architecture directed by hydrogen bonding. Complex 3 exhibits a three-dimensional structure; Schl?fli symbol of {4⁴·6¹⁰·8}. The luminescent property of compound 3 is discussed.     

Construction of Two New Metal–Organic Frameworks from Pamoic Acid and N-Containing Auxiliary Ligands

Two new metal–organic frameworks; namely, [Cd₂(pam)₂(bpe)_1.5(DMF)₂(H₂O)] _n ·2n(DMF) (1) and [Cd(pam)(bix)] _n (2) (H₂pam = pamoic acid, bpe = 1,2-di(4-pyridyl)ethylene, bix = 4,4′-bis(imidazol-1-ylmethyl)benzene, DMF = N,N′-dimethylformamide), were solvothermally synthesized via varying the auxiliary ligand. Single crystal X-ray diffraction analysis reveals that compound 1 shows a 2D→3D polythreaded motif based on (3,4)-connected 2D sheets, while compound 2 features a 4-connected sql tetragonal plane net, which further extended into a 3D supramolecular framework through intermolecular CH···π interactions. In addition, the luminescent and thermal stabilities properties of these two compounds were investigated.     

One-Dimensional Cd(II) and Co(II) Coordination Polymers with Dinuclear Secondary Building Units Constructed by 1,1′-Biphenyl-3,3′-Dicarboxylic Acid: Synthesis, Structures, Luminescent and Magnetic Properties

Bilayered diffusion and hydrothermal synthetic methods using pyridine (py) and 2,6-dimethylpyrazine (dmpz) as weak bases and small terminal ligands generated two Cd(II) and Co(II) 1D coordination polymers with dinuclear metal clusters as secondary building units (SBUs) from an organic bridging ligand, 1,1′-biphenyl-3,3′-dicarboxylic acid (H₂ L). They are {[Cd₂(L)₂(py)₄] (py)(CH₃OH)} _n (1) and [Co₂(L)₂(dmpz)₄(H₂O)] _n (2). Compounds 1 crystallizes in the monoclinic space group P2(1)/c, while 2 crystallizes in the triclinic space group P-1. Especially, compound 2 possesses the 1D chain structure that contains two linked left-handed and right-handed helices. Fluorescent measurements for 1 display strong blue light emissions with the maximum emission at 396 nm with the excitation of 320 nm. Magnetization study shows the existence of weak antiferromagnetic coupling for 1 with the negative −E ₂/k value of −1.3 K.     

Synthesis and Changes of Conductivities and Thermal Stabilities of 4,4′-Oxybis [N-(3,4-Dihydroxybenzilidene) Aniline] Chelate Polymers

In this study novel metal coordination polymers were synthesized such as poly-4,4′-oxybis[N-(3,4-dihydroxybenzilidene)aniline] (P-3,4-HBA) containing Cu, Co, Pb, Ni, Zn, Cd, Cr, Mn and Zr metals in the polymer backbone. The polymers are abbreviated as P-3,4-HBA-Cu, P-3,4-HBA-Co, P-3,4-HBA-Pb, P-3,4-HBA-Ni, P-3,4-HBA-Zn, P-3,4-HBA-Cd, P-3,4-HBA-Cr, P-3,4-HBA-Mn and P-3,4-HBA-Zr, respectively. To confirm the structures FT-IR, UV-vis, ¹H and ¹³C-NMR spectral techniques were used. Additional characterization of the polymers was made by size exclusion chromatography (SEC), TGA-DTA and solubility tests. By TGA analysis, P-3,4-HBA-Zr was the most stable polymer against thermal degradation among those synthesized. In addition, it was found that, with exception of P-3,4-HBA-Cr, the other synthesized polymers have little solubility in many organic solvents and water. According to SEC results, P-3,4-HBA-Cr has a single fraction containing 21–22 mer units. Electrical conductivities of the monomer and polymers were measured by the four-point probe technique. The polymers were semiconductors; and, some of their conductivities can be increased via doping with iodine. According to the electrical conductivities of the undoped P-3,4-HBA-Cr and P-3,4-HBA-Zr polymers have nearly ten-times higher conductivities in comparison to the others. From UV-vis measurements, the optical band gaps (E _g ) of 3,4-HBA and P-3,4-HBA-Cr were 2.58 and 2.39 eV, respectively. This result indicates that P-3,4-HBA-Cr has a lower band gap and consequently higher electrical conductivity than 3,4-HBA. Thus, with good solubility, high electrical conductivity and high thermal stability P-3,4-HBA-Cr may be considered as the most useful metal coordination polymer among those synthesized.