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。     

含吡咯亚胺铜配合物的合成、表征及晶体结构

合成了一种新型含吡咯亚胺铜配合物,用元素分析、红外光谱及X射线单晶衍射对其进行了表征。结构解析表明,每个铜配合物分子含有两个吡咯亚胺配体,每个配体用两个氮原子与中心金属铜离子螯合,每个铜离子均采取平面四边形构型与配体中的四个氮原子配位。     

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。     

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.     

Synthesis, Characterization and Crystal Structure of a Novel One-Dimensional Supramolecular Dimethyltin (IV) Compound

A novel one-dimensional (1D) supramolecular dimethyltin compound of (Me₂SnO)₂(Me₂SnOCH₃)(O₂CCH₂SC₄H₃N₂-2,6)[Me₂Sn(O₂CCH₂SC₄H₃N₂-2,6)₂]·CH₃OH was prepared by the reaction of (CH₃)₂SnCl₂ with (2-pyrimidylthio)acetic acid with CH₃ONa as a base. The title compound contained four different tin atom environments. Among them, Sn(1) and Sn(2) were both five-coordinate with distorted trigonal bipyramidal geometries, Sn(3) was six-coordinate with a distorted octahedral geometry and Sn(4) was seven-coordinate with pentagonal bipyramidal geometry. Meanwhile, the compound was stabilized in a 1D infinite chain by intermolecular Sn–O bonds. An erratum to this article can be found at     

A Mixed Valence Copper Cyanide 3D-supramolecular Coordination Polymer Containing 1,10-Phenathorline Ligand as a Potential Antitumor Agent, Effective Catalyst and Luminescent Material

The structure of the 3D-supramolecular coordination polymer (SCP) _∞³{[Cu^Ι(CN)·2(phen)·Cu^ΙΙ(CN)₂·(phen)]·5H₂O}, 1 contains the [Cu^Ι(CN)·2(phen)], [Cu^ΙΙ(CN)₂·(phen)] molecular complexes and five water molecules which are connected with each other by hydrogen bonds. The most intriguing feature in the structure of 1 is the unusual supramolecular interactions, including hydrogen bonds which involve the terminal cyanide and the phenanthroline (phen) ligands and π–π stacking which generate a unique 3D-supramolecular architecture in the solid state. The emission spectrum of 1 displays a band centered at 420 nm which was assigned to S_o-T transition in the CuCN fragments. This band suffers a shift to longer wavelength by about 30 nm than that of CuCN itself. The emission bands at 435, 450, and 475 correspond to the close laying π–π* transitions of the coordinated phen. The main band at 435 nm exhibits a red shift than that of phen by about 70 nm which makes it attractive as luminescent sensor. Also, the SCP 1 was used as heterogeneous catalyst for the degradation of Metanil Yellow (MY) dye by dilute solution of hydrogen peroxide as oxidant. The reaction is first order with respect to the MY dye. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was used to determine the in vitro antitumor activity of the SCP 1 on human breast cancer cell line, MCF7. The cytotoxicity of the SCP 1 is more efficient than that of the Doxorubicin (DOX) drug. The thermal stability has been also investigated.     

Synthesis,Crystal Structure and Luminescent Property of a New Zn(II) Coordination Polymer with Twofold Interpenetrated pcu Topology

A new Zn(II) coordination polymer; namely, [Zn(FA)(bmix)_0.5] _n ·nH₂O (1, H₂FA = fumaric acid, bmix = 1,4-bis(2-methyl-1H-imidazol-1-ylmethyl)benzene) was synthesized with fumaric acid and flexible 2-methylimidazole-based ligands with Zn(II) salts under hydrothermal conditions. Single-crystal X-ray diffraction reveals that 1 features a twofold interpenetrating three-dimensional pillar-layered framework based on paddle-wheel shaped [Zn₂(COO)₄] subunits. The structure may be simplified to a 6-connected pcu topological network. Luminescent investigation reveals that 1 exhibits intense ligand-centered fluorescence at room temperature.     

新型偶氮类聚硅氧烷液晶的合成及表征

通过对硝基苯胺和苯酚的重氮化反应合成了端基为硝基的刚性基元,再经醚化、加成、酯化反应,合成了偶氮类聚硅氧烷液晶.通过IR、1H NMR对该化合物的结构进行了鉴定,并用POM、DSC对其液晶行为进行了表征.结果表明,该化合物属于近晶A型液晶,相变区间为155.558～226.381℃.     

A 3D 3d-4f Heterometallic Coordination Polymer: Synthesis,Crystal Structure and Properties

Abstract  A three-dimensional heterometallic coordination polymer formulated as Sm₂Zn₂(BIPA)₅(H₂O)₂ (1) (H₂BIPA = 5-bromoisophthalic acid) was synthesized by hydrothermal reaction of H₂BIPA with Sm₂O₃ and Zn(NO₃)₂. Complex 1 shows an 8-connected (3⁶.4¹⁸.5³.6) topological network. The thermal analysis of complex 1 has been measured and discussed. Additionally, the photoluminescent property of complex 1 was investigated. Graphical Abstract  An intriguing feature of complex 1 is a 3D eight-connected framework of 3⁶.4¹⁸.5³.6 topology.      

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.     

Supramolecular Structure,Mode of Coordination,Thermal and Potentiometric Studies of Polymer Complexes: A Review

Chelating compounds derived from acryloyl monomers are being utilized as suitable ligands. They enable the formation of rigid coordination polymers. This review gives information about preparation and structurally characterization the polymer complexes by analyses, spectral techniques like IR, NMR, ESR thermal and potentiometric methods. The ESR spectral data of the Cu(II) complexes showed that the metal–ligand bonds have considerable covalent character. The thermal stability was investigated using thermogravimetric analysis. The thermal behavior of these chelates shows that the hydrated complexes lose water molecules of hydration in the first step followed immediately by decomposition of the anions and ligand molecules in the subsequent steps. The results showed that the polymer complexes are more stable than the homopolymer. Proton ligand dissociation and metal ligand stability constants of acryloyl monomers with some transition metal ions in monomeric and polymeric forms potentiometrically were determined.     

三维网状配位聚合物[Mn5（suc）4（OH）2]n的合成与晶体结构

水热法合成了一种配位聚合物：[Mn5（suc）4（OH）2]n（H2SUC=丁二酸）,并通过元素分析、红外光谱进行了表征,用X-射线单晶衍射仪测定了配合物晶体结构。配合物属于单斜晶系,P21／C空间群,黠胞参数：a=9．572（2）,b=9．647（2）,c=12．526（3）A,V=1147．9（4）A3,Z=2,De=2．236g／cm^3,F（000）=766,μ（MoKa）=2．767mm^-1。对于2098个可观察到的衍射点（I〉2σ④（I））,R1=0.0292和WR2=0．0610。配合物是一个柱层式的兰维网状结构。     

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.     

Structure and Spectral Characteristics of 3D-Supramolecular Coordination Polymers Based on Copper Cyanide and Dimethylquinoxaline

The reactions of K₃[Cu(CN)₄], R₃SnCl (R = Me or ph) and 2,3-dimethyl quinoxaline (dmqox) in H₂O/acetonitrile media at room temperature afford the 3D-supramolecular coordination polymers (SCP) ³_￥ [ \textCu ₂ ( \textCN ) ₂ \textdmqox ] ^{ 3}_{\infty } \left[ {{\text{Cu}}_{ 2} \left( {\text{CN}} \right)_{ 2} {\text{dmqox}}} \right] , 1 and ³_￥ [ \textCu ₂ ( \textCN ) ₄ ·( \textPh ₃ \textSn ) ₂ ·\textdmqox ] ^{ 3}_{\infty } \left[ {{\text{Cu}}_{ 2} \left( {\text{CN}} \right)_{ 4} \cdot \left( {{\text{Ph}}_{ 3} {\text{Sn}}} \right)_{ 2} \cdot {\text{dmqox}}} \right] , 2. The structure of the tin free 1 consists of parallel zigzag chains connected by dmqox to form 2D-sheets containing hexagonal 18-atom fused Cu₆(CN)₄(dmqox)₂ rings. The interwoven sheets along the a axis are close packed by extensive H-bonds developing 3D-network structure. The structures of 1 and 2 are investigated by elemental analysis IR, NMR and mass spectra. The ESI⁺ and ESI⁻ mass spectra of 2 support its polymeric nature while the ESI⁺ mass spectrum confirms the expected M. W. suggested by elemental analysis. The ¹³C-NMR spectrum of 2 supports the fact that the network structure of 2 contains the rhombic [Cu₂(μ₃-CN)₂] motif. The structure of 2 was compared with the structure of the reported prototype ³_￥ [ \textCu ₂ ( \textCN ) ₄ ·( \textPh ₃ \textSn ) ₂ ·\textqox ] ^{ 3}_{\infty } \left[ {{\text{Cu}}_{ 2} \left( {\text{CN}} \right)_{ 4} \cdot \left( {{\text{Ph}}_{ 3} {\text{Sn}}} \right)_{ 2} \cdot {\text{qox}}} \right] as well as the other related structures.