Silver(I) Coordination Polymer Based on a Schiff Base Ligand: Synthesis,Crystal Structure and Luminescent Properties

A new Ag(I) coordination polymer [AgL(NO₃)] _n 1 (L = 4-benzoylpyridine hydrazone) has been synthesized and characterized by IR, UV, elemental analysis, thermogravimetry and X-ray crystallography. Ag(I)-atom has a seesaw environment with a set of donors from three N-atoms of three ligands and one O-atom from one NO₃ ⁻ anion. Each ligand is bonded to three silver centers and each silver atom is coordinated by three ligands thereby generating two types of bimetallic metallocyclic unit to form a 1D chain. The 1D chains interact each other giving further rise to a 3D supramolecular network through multiform intermolecular hydrogen bonds. The luminescent properties of the polymer 1 at room temperature were investigated.     

三维锌孔道配位聚合物的合成及结构

在DMF/H2O/C2H5OH混合体系中,以2-(4-吡啶)-咪唑二羧酸为有机连接体与Zn2+反应得到了一个新的含有孔道的三维锌配位聚合物,分子式为:Zn3(HL)3(DMF)2.2DMF,H3L=2-(4’-吡啶)-咪唑二甲酸,DMF=N,N-二甲基甲酰胺。单晶X射线分析显示1是带有一维矩形孔道的三维开骨架结构,孔道直径大小为18.28×6.952。     

基于含铜簇配位聚合物的制备及晶体结构

通过席夫碱配体2-羟基-3-甲氧基-苯甲醛缩烟酰肼(IAH)和碘化亚铜在溶剂热条件下得到新型的铜(I)配位聚合物[(Cu2I2)L]n。通过元素分析、红外光谱和热重分析等方法对该配合物进行了表征,并测定了它的单晶结构。配合物属三斜晶系,空间群P-1,a=7.998 8(8)?,b=12.642 3(12)?,c=17.919 7(17)?,α=89.528(2)°,β=89.528(2)°,γ=73.688 0(10)°,V=1 738.9(3)?~3,Z=2。     

Solvothermal Synthesis and Crystal Structure of a Novel 3D Triorganotin Polymer Containing Polyfunctional Ligand 5-mercapto-1(H)-tetrazoleacetic acid

A novel 3D tri-n-butyltin complex [(n-Bu₃Sn)₂(C₂H₂N₄SCO₂)]_n (1) has been solvothermally synthesized and structurally characterized by elemental analysis, FT-IR, NMR (¹H, ¹³C, and ¹¹⁹Sn) spectra and X-ray crystallography. X-ray data of complex 1 reveals that it is a 3D tri-n-butyltin coordination polymer with a metal-organic framework (MOF) structure , significant N → Sn interactions plays an important role in the construction of this structure.     

Synthesis, Crystal Structure and Antitumor Activity of Ca(II) Coordination Polymer Based on 1,5-Naphthalenedisulfonate

A novel Ca(II) coordination polymer, [CaL(H₂O)₂] _n (L = 1,5-naphthalenedisulfonate), was synthesized by reaction of calcium perchlorate with 1,5-naphthalenedisulfonic acid sodium in CH₃CH₂OH/H₂O. It was characterized by elemental analysis, IR, ¹HNMR and thermal analysis. X-ray crystallographic reveals that the Ca(II) coordination polymer belongs to triclinic system, with space group P-1. The geometry of the Ca(II) ion is a distorted CaO₆ octahedron coordination environment, arising from its coordination by two water molecules, and four oxygen atoms from two l ligands. The Ca(II) ions are linked through the O atoms of 1,5-naphthalenedisulfonate ligands to form 1D chain structure. And then a 2D layered structure is constructed by hydrogen bonds and π–π stacking. The antitumor activity of 1,5-naphthalenedisulfonic acid sodium ligand and its Ca(II) coordination polymer against human hepatoma smmc-7721 cell line and human lung adenocarcinoma A549 cell line have been investigated.     

Cadmium(II)-N-Ethylimidazole Coordination Polymer via Different Coordination Environment and Chloro Bridges: Synthesis, X-ray Structure, Spectroscopic and Thermal Analysis

A novel coordination polymer [Cd₂(μ-Cl)₄(Neim)₃]_n (1) (Neim = N-ethylimidazole) was synthesized and structurally characterized by means of elemental analysis, thermal analysis, FT-IR spectrum and single-crystal X-ray diffraction. There are two different cadmium centers in 1. One of these metal centers has octahedral geometry, while the other has square pyramidal geometry. Two Neim ligands are coordinated to the Cd(II) ion in octahedral geometry while one Neim ligand is coordinated to the Cd(II) ion in square pyramidal geometry. Relatively weak C–H···Cl interactions between N-ethylimidazole molecules and chloro ions in the complex play an important role in the construction of a three-dimensional supramolecular framework. Complex 1 exhibits photoluminescence emission in solid state at room temperature.     

Synthesis, Crystal Structure and Magnetic Properties of a Nickel(II) Coordination Polymer Based the V-Shaped Ligands

Abstract  

A new nickel(II) coordination polymer, Ni₂(DBA)₂(BIDPE)₂(H₂O) (1) (H₂DBA = 4,4′-methylenedibenzoic acid and BIDPE = 4,4′-bis(imidazole-l-yl)diphenyl ether), has been prepared by hydrothermal synthesis and structurally characterized by IR, elemental analysis, TGA and single crystal X-ray diffraction. Complex 1 features a one-dimensional chain structure based on triply bridged binuclear units, which is further interlinked into a higher-dimensional supramolecular framework by intermolecular weak interactions. Variable-temperature magnetic data shows weak antiferromagnetic behavior in 1.     

In situ Synthesis,Crystal Structure and Photoluminescence of a Novel Coordination Polymer with (4,6,6)-Connected sqc111 Topology

Employing the mixed ligands to react with Cd(NO₃)₂·4H₂O afforded a new 3D coordination polymer [Cd₃(BPTC)(bmp)₂(ox)(H₂O)₄] (1) (H₄BPTC?=?biphenyl-3,3′,4,4′-tetracarboxylic acid, bmp?=?3,6-bis(imidazol-1-yl)pyridazine, H₂ox?=?oxalic acid), in which ox^2? was from the in situ oxidation of ethanol. Compound 1 bears a novel trinodal (4,6,6)-connected net structure, and it is the first replica of the theoretically predicted sqc111 topology net. Moreover, the thermal and photoluminescent properties for 1 were also investigated.     

A Novel 3D Europium (III) Coordination Polymer Constructed from 3,5-Pyridinedicarboxylate Acid: Synthesis, Crystal Structure and Emission Spectrum

Abstract  A novel 3D coordination polymer Eu₂(PDC)₃(H₂O)₃ (1) has been synthesized by hydrothermal reaction of europium chloride with 3,5-pyridinedicarboxylate acid (H₂PDC) under acidic condition (pH 2–3). Complex 1 is a 3D coordination polymer via 1D infinite chains built by the pyridinium moieties of the PDC²⁻ anions. The thermal analyses and luminescent properties of 1 have also been investigated. Graphical Abstract   A novel 3D coordination polymer Eu₂(PDC)₃(H2O)₃ has been synthesized by hydrothermal reaction of europium chloride with 3,5-pyridinedicarboxylate acid under acidic conditions (pH 2–3). The formation of the title complex demonstrates that pH plays an important role during the synthesis.      

Synthesis, Crystal Structure, Spectroscopic and Thermal Properties of a Novel Complex of Hydantoin-5-acetic acid with Co(II)

The complex, tetraaqua bis(hydantoin-5-acetato) cobalt(II) was synthesized by the reaction of hydantoin-5-acetic acid and CoCl₂·6H₂O presence of NaHCO₃. The structure of the complex was determined by X-Ray single crystal data the thermal analyses, FT–IR and magnetic susceptibility data are also presented. The monoclinic crystal of the title compound, [Co(C₅H₅N₂O₄)₂(H₂O)₄], lie across centers of inversion in space group P21/c. The complex features a distorted octahedral [CoO₆] coordination with hydantoin-5-acetato and water ligands. The hydantoin-5-acetato anion is bonded to the cobalt(II) ion via its deprotonated carboxylic acid O atom. The complex molecules show three dimensional supramolecular networks by O–H···O and N–H···O interactions.     

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

The 2D coordination polymer, [Zn(dpa)(bpp)] _n (H₂dpa = 2,4′-biphenyl-dicarboxylic acid, bpp = 1,3-di(4-pyridyl)propane) was prepared by hydrothermal synthesis in the presence of NaOH and characterized by single-crystal X-ray diffraction, FTIR spectra, element analysis and thermal analysis. The crystal structure determination reveals that the carboxylate groups of 2,4′-biphenyldicarboxylic acid are acting as bridging ligands and adopt two coordination modes; bis-monodentate and bidentate chelating. The network consists of a 2D (6,3)-connected architecture. At room temperature the solid-state luminescence spectrum of [Zn(dpa)(bpp)] _n shows a blue emission at about 354 nm upon excitation at 333 nm.     

一维NiⅡ配合物的合成、结构及热稳定性

在甲醇-水溶剂中,用四溴代对苯二甲酸(H2TBTA)、1,3-二(4-吡啶基)丙烷(BPP)、硝酸镍为原料合成了一维链状配合物[Ni(BPP)2(TBTA)(H2O)2]n。该配合物晶体中NiII金属离子与两个BPP的两个N原子、两个H2TBTA中的两个羧基O原子及两个水分子中的O原子配位,形成六配位的变形八面体结构。晶胞参数:三斜晶系,P-1空间群,a=9.444(5),b=9.602(5),c=11.356(6),V=882.2(8)3,Z=1,Dcalc=1.828 mg/mm3,R1[I>2σ(I)]=0.0329,wR2(all data)=0.1058。对晶体进行热稳定性分析表明:配合物在122℃以下稳定性良好。     

A New 3D Coordination Polymer Based on Pentanuclear Cd(II) Rod-Shaped Secondary Building Unit: Synthesis,Crystal Structure and Luminescent Property

A new coordination polymer [Cd_2.5(μ₃-OH)(L)₂(bipy)]_n (1). (L = 1,2-naphthalene dicarboxylate, bipy = 4,4′-bipyridine), was obtained under hydrothermal condition. The structure of 1 has been determined by single-crystal X-ray diffraction analysis and further characterized by elemental analysis and IR spectrum. Single-crystal X-ray diffraction analyses reveal that complex 1 crystallizes in triclinic system, Pī space group. Complex 1 possesses a 3D pcu net based on a pentanuclear Cd(II) cluster. Each pentanuclear Cd(II) cluster links with neighboring ones and generates a rod-shaped secondary building unit, which is further extended by bipy ligands to forms a three-dimensional network. Furthermore, the luminescent properties of this complex and the free ligand have been investigated. Complex 1 can be excited directly and emit strong soild-state fluorescence at room temperature, which may make them excellent candidates for fluorescent materials.     

A Novel Binodal (4,9)-Connected 3D Calcium Coordination Polymer: Synthesis, Characterization, Thermal Stability and Luminescent Properties

A novel coordination polymer, namely, [Ca₃(BIPA)₃(H₂O)₃·H₂O] _n (1) has been prepared by the reaction of 5-bromoisophthalic acid (H₂BIPA) with corresponding Ca(II) ions, and characterized by single-crystal X-ray diffraction, element analysis, infrared spectroscopy, thermogravimetric analysis In compound 1, a trimer unit [Ca₃O₁₉] is bridged the carboxylate oxygen atoms, forming an inorganic layer structure. The inorganic layers are linked by the BIPA^2? ligands, resulting in a three-dimensional (3D) pillared layered structure with a binodal (4,9)-connected 3D net structure with Schläfi symbol of (3⁴·4²)(3⁸·4¹⁰·5¹²·6⁶). In compound 1, the carboxylate groups of the BIPA^2? ligands coordinate to calcium ions using different coordinated modes. In addition, the thermal stability and luminescent properties of 1 were also investigated.