Synthesis,Crystal Structure and Fluorescence Property of the Ag(Ⅰ) Coordination Polymer Constructed by 2D[Ag(1,3-BIP)(PMA)_(0.5)]_n^(n-)Layers and 1D[Ag(1,3-BIP)(H_2O)]_n^(n+) Chains

A new AgO） coordination polymer, {[Ag（1,3-BIP）（H20）][Ag（1,3- BIP）（PMA）0.5.- 4H20}n （PMA = 1,2,4,5-benzenetricarboxylic acid, 1,3-BIP = 1,3-bis（imidazole）propane）, have been synthesized and characterized by single-crystal X-ray diffraction, powder XRD, FTIR, TGA and elemental analysis techniques. The single-crystal X-ray diffraction reveals that the title complex is formed by 1D polymeric cationic chains of [Ag（1,3-BIP）（H2O）]n^n＋ and 2D polymetric anionic layer of [Ag（1,3-BIP）（PMA）0.5]n^n-, which are further linked by intermolecular H-bonding to form a 3D supramolecular framework. In addition, the photoluminescence property of the title complex in the solid state at room temperature was also investigated.

A New Cd(Ⅱ)Coordination Compound Based on 4-(1,2,4-Triazol-4-yl)phenylacetic Acid:Synthesis,Structure and Photoluminescence Property

A new complex [Cd2（L）2（Cl）2（H2O）]n（1） was synthesized by reacting CdCl2·2.5 H2O with 4-（1,2,4-triazol-4-yl）phenylacetic acid（HL） ligand.The structure of the complex was characterized by single-crystal X-ray diffraction,IR spectroscopy,elemental analysis and PXRD.Complex 1 crystallizes in triclinic,space group P21/c with a = 11.4303（8）,b = 14.1792（10）,c = 14.6857（10） ？,β = 96.3780（10）o,V = 2365.4（3） A^3,Z = 4,C（20）H（16）Cl2N6O5Cd2,Mr = 716.09,Dc = 2.011 g/cm3,μ = 2.069 mm^-1,S = 1.051,F（000） = 1392,the final R = 0.0458 and wR = 0.0949 for 5402 observed reflections（I 〉 2σ（I））.Complex 1 is a two-dimensional（2D） layer structure and non-covalent bonding interactions such as C–H···π and π···π extend the 2D to form a three-dimensional supramolecular polymer.

Ionothermal Synthesis, Crystal Structure and Photocatalytic Property of a New Cobalt Coordination Polymer

The reaction of flexible bis（imidazole） ligand and 1,2-bis（imidazol-l＇-yl）methane （bimm） with Co（Ⅱ） salt under ionothermal method resulted in the formation of a new coordination polymer {[Co（bimm）3]·（PF6）2}n （1）. X-ray single-crystal diffraction determination reveals that 1 crystallizes in the triclinic Pi space group, with α = 8.647（6）, b = 12.092（9）, c = 14.967（1 l） A, α = 88.912（8）, β = 81.199（8）, ）, = 89.395（8）°, V= 1546 （2） A3, Z = 2, Mr = 793.39, Dc= 1.704 Mg/m3,μ = 0.768 mm-1 F（000） = 798, the final R = 0.0626 and wR = 0.1634 for 4319 observed reflections with I〉 2σ（I）. In compound 1, the Co（lI） ion is connected to another Co（ll） by two bimm ligands to form 1D double chains which are further linked by bimm ligands to form a 2D wavelike layer. Topologically, the structure of 1 represents a uninodal 2D 4-connected sq1/Shubnikov tetragonal plane net. Moreover, thermogravimetric analyses and photocatalytic property for 1 have also been investigated.

Syntheses,Structures and Photoluminescent Properties of Cd(Ⅱ)Polymeric Complexes Based on 5-Aminoisophthalic Acid and Bipyridine Co-ligands

Two novel complexes, namely {[Cd（AIP）（4,4＇-bpy）]·1.3DMF}n（1） and [Cd（AIP）（2,2＇- bpy）]n（2）, have been synthesized through solvothermal reaction（H2AIP = 5-aminoisophthalic acid, 2,2＇-bpy = 2,2＇-bipyridine, 4,4＇-bpy = 4,4＇-bipyridine, and DMF = N,N＇-dimethylformamide） and structurally determined by single-crystal X-ray diffraction. Complex 1 shows a three-dimensional（3D） layer-pillar framework with rectangular channels, while complex 2 displays a two-dimensional（2D） wave net architecture. Furthermore, 1 and 2 were characterized by elemental analysis, infrared spectra（IR）, thermal gravimetric analyses（TGA） and fluorescence measurements. The luminescent properties of 1 dispersed in various organic solvents have been investigated systematically, demonstrating high selectivity for acetone via the fluorescence quenching effect.

Solvothermal Synthesis,Crystal Structure and Photoluminescence Property of a 3D Lead(Ⅱ)Coordination Polymer Based on Terephthalic Acid

Solvothermal reaction of Pb（NO3）2·6H2O with rigid linear ligand terephthalic acid（H2pta） in N,N-dimethylformamide（DMF） produced a new three-dimensional（3D） lead（Ⅱ）coordination polymer[Pb2（pta）1.5（μ4-OH）（DMF）]n 1,and its structure was characterized by single-crystal X-ray diffraction analyses.In polymer 1,the μ4-OH bridges the nearby lead（Ⅱ） ions into an infinite one-dimensional（1D） chain,and then the organic ligand pta^2- joins the neighbored chains into a 3D structure by two similar connection modes in different configurations.The solid-state photoluminescent studies revealed that 1 exhibits a strong greenish emission mainly originating from ligand-to-metal charge transfer between the delocalized π bonds of the aromatic carboxylate ligand pta^2- and the p orbitals of the Pb^2＋ centers.

Synthesis,Structure and Photoelectric Property of a 3D Supramolecular Zinc Coordination Polymer

Using a rigid azo ligand 4-[（8-hydroxy-5-quinolinyl）azo]-benzoic acid（H2 L）,a new supramolecular compound [Zn（L）（H2O）2]n（1） has been solvothermally synthesized and structurally characterized by X-ray single-crystal diffraction,infrared spectrum,elemental analysis,power X-ray diffraction and thermal analysis.Compound 1 crystallizes in monoclinic,space group C2/c with a = 30.372（8）,b = 11.415（3）,c = 9.248（3） A,β = 106.94（3）o,V = 3067.20（15）A3,C（16）H（13）N3O5Zn,Mr = 392.66,Z = 8,Dc = 1.701 Mg/m^3; F（000） = 1600,μ = 1.636 mm^-1,reflections collected：7290,reflections unique：2735,R（int）= 0.0282,R = 0.0351,wR（all data） = 0.0919,GOOF on F^2 = 1.036.Compound 1 exhibits a one-dimensional（1 D） zig-zag chain structure connected into a three-dimensional（3D） supramolecular network through hydrogen bonding interactions.Fluorescent property and electrochemical property were detected on compound 1.

Hydrothermal Synthesis,Crystal Structure and Properties of a 1D Chain Copper(Ⅱ) Polymer with 3-(2-Pyridiyl)-1H-1,2,4-triazole(Hpt)

A new 1D copper（Ⅱ） polymer [Cu（Hpt）（3,5-DMBA）]n has been hydrothermally synthesized with copper acetate,3-（pyridin-2-yl）-1,2,4-triazole（Hpt） and 3,5-dimethylbenzoic acid（3,5-DMBA）. It crystallizes in triclinic space group P1,with a = 8.1974（6）,b = 8.3280（6）,c = 12.5021（9） ？,α = 84.3320（10）,β = 71.8870（10）,γ= 65.4560（10）o,V = 737.44（9） ？~3,Dc = 1.612 g/cm3,Z = 2,F（000） = 366,GOOF = 1.035,R = 0.0298 and w R = 0.0855. The crystal structure is a one-dimensional（1-D） chain in which the Cu（Ⅱ） is five-coordinated with square pyramidal geometry. The crystal structure shows that the whole molecule consists of two copper ions bridged by two μ12-η：η0-3,5-dimethylbenzoic acid anions and two 3-（pyridin-2-yl）-1,2,4-triazole molecules. The coordination environment of Cu（Ⅱ） ion is CuO＋2N_3. The luminescence and thermal properties of the complex were investigated.

Syntheses,Crystal Structures,and Magnetic Properties of Two Manganese(Ⅱ) Coordination Polymers Based on Bifunctional Pyridine-benzene Carboxylic Acids

Two manganese（II） coordination polymers, namely, {[Mn（PIP）（BIBP）]·（BIBP）0.5}n（1） and {[Mn（PTA）（BIMBP）（H2O）]·H2O（0.69）}n（2）（H2PIP = 5-（4-pyridyl）-isophthalic acid, H2 PTA =6-（4-pyridyl）-terephthalic acid, BIBP = 4,4？-bis（imidazol-1-yl）biphenyl, and BIMBP =4,4？-bis（imidazol-1-ylmethyl）biphenyl）, have been synthesized by using the bifunctional pyrinde-benzene carboxylic acids and bis（imidazole） linkers as mixed ligands to react with Mn SO4,and further characterized by elemental analysis, IR, and PXRD. Compound 1 is in the triclicnic system, space group P1 with a = 10.1089（8）, b = 13.1927（12）, c = 14.0638（12）A, α = 69.437（2）, β= 73.2890（10）, γ = 78.5320（10）o, V = 1671.9（2） A^3, Z = 2, Dc = 1.449 g/cm^3, F（000） = 705,μ（MoK α） = 0.453 mm^-1, S = 1.053, R = 0.0491 and wR = 0.1367 for 5837 unique reflections（Rint =0.0208） with I 〉 2σ（I）. Compound 2 belongs to the monoclicnic system, space group C2/c with a =15.199（3）, b = 19.731（3）, c = 21.537（5） ？, β = 105.228（3）o, V = 6232（2） A^3, Z = 8, Dc = 1.363g/cm^3, F（000） = 2648, μ（MoK α） = 0.475 mm^-1, S = 1.048, R = 0.0489 and wR = 0.1151 for 7414 unique reflections（Rint = 0.0425） with I 〉 2σ（I）. Structural analyses reveal that complex 1 is a4-connected（44.62）-sql bilayer structure with binuclear [Mn2（COO）2] SBU, while complex 2 is a normally（3,5）-connected（42.67.8）（42.6）-3,5L2 monolayer. And the sheets interacted with the adjacent sheets through weak interactions, finally giving a stable three-dimensional（3D）supramolecule. Besides, the variable-temperature magnetic susceptibility measurement of complex1 was investigated.

Two Cobalt(Ⅱ)Coordination Polymers Based on Tetrazylphosphonate and Tetrazylphosphonic Acid Ligands

Two cobalt coordination polymers with the same 2D structure have been hydrothermally synthesized based on two bifunctional ligands with tetrazole and phosphonate（phosphonic acid） groups,namely,diethyl 4-（2H-1,2,3,4-tetrazol-5-yl） benzylphosphonate（C_2H_5-L1） and 4-（2H-1,2,3,4-tetrazol-5-yl）benzylphosphonic acid（H_2L2）. The structures of the two complexes are characterized by elemental analysis,IR,TGA and X-ray single-crystal/powder diffraction. The pink block crystals of complex [Co（L1）（H_2O）]·H_2O（1） belong to the monoclinic system,space group C2/m with a = 20.8390（11）,b = 7.2695（3）,c = 10.0156（6） A,β = 109.773（7）°,V = 1427.80（13） A^3,Z = 4,D_c = 1.680 mg/cm^-3,M_r = 361.16,F（000） = 740,R = 0.0316 and wR = 0.0826 for 1702 observed reflections（I 〉 2σ（I））. The purple block crystals of complex [Co（L2）（H_2O）]·2H_2O（2） also belong to the monoclinic system,space group C2/c with a = 25.5382（16）,b = 7.3844（3）,c = 15.1925（11） A,β = 124.238（9）°,V = 2368.6（2） A^3,Z = 8,D_c = 1.969 mg/cm^-3,M_r = 351.12,F（000） = 1432,R = 0.0475,wR = 0.1617 for 2088 observed reflections（I 〉 2σ（I））. Both the nitrogen atoms of tetrazole group and oxygen atoms of phosphonate（phosphonic acid） groups in the ligands coordinated with the metal cobalt. The magnetic property of complex 1 is also investigated.

Syntheses and Crystal Structures of Two Copper(Ⅱ) Coordination Polymers Derived from Aromatic Carboxylic Acids and Bis(imidazoles)Ligands

Two compounds have been obtained by the reaction of metal（Cu（II））, 4,4＇-bis（imidazol-l-yl）diphenyl thioether（BIDPT） with two carboxylic acids, 4,4＇-oxydibenzoic acid（H2oba） and phthalic acid（H2pht）. The crystal structures of the resulting compounds, namely {[Cu（BIDPT）（oba）]·H2O}n（1） and {Cu（BIDPT）（pht）}n（2）, have been determined by single-crystal X-ray diffraction analysis. Compound 1 is of orthorhombic system, space group Pbcn with a = 27.8310（3）, b = 10.7791（1）, c = 19.3913（2）A, V = 5817.0（3） ？3 and Mr = 656.15. Compound 2 belongs to the monoclinic system, space group C2/c with a = 18.2678（2）, b = 11.0259（1）, c = 22.906（2） A, β = 97.727（2）o, V = 4571.8（8） A3 and Mr = 545.04. Structural analyses reveal that compounds 1 and 2 respectively exhibit two-dimensional（2D） wavy and corrugated layer structures. Through intermolecular hydrogen bonding, compound 1 is assembled into a 3D supramolecular structure. The thermal stability and ultraviolet spectroscopy properties of the two compounds are also investigated.

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）·nH2O（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 A,α = 88.487（3）,β = 72.529（3）,γ = 79.991（3）°,V = 2009.8（5）A^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.

Effect of CF and RPP on the Mechanical and Electrical Properties of Smart Aggregate

By using redispersible polymer powder（RPP） and carbon fiber（CF） to adjust the flexibility and electrical properties of the smart aggregate, a new kind of smart aggregate with Z type structure was proposed. The study shows that Z type aggregate is more sensitive to the feedback of external force than the prism aggregate in the same loading environment, and it indicates that Z type aggregate is more suitable for the research and application of concrete health monitoring. Although the incorporation of RPP would cause the compressive strength of the aggregates and the elastic modulus of hardened cement mortar to reduce slightly within the dosage of RPP by 2.25% because of the polymer film formed in the internal system, this would improve the deformability of the aggregates. In the early loading stage（in the first 60 seconds）, the intelligent concrete specimens implanted with Z type smart aggregate do not show higher sensitivity as expected, although the resistance change rate changes a little bit more, the overall of it is still in balance. Adding RPP could improve the flexibility of smart aggregates exactly, and it plays an active role in prolonging the life of the smart aggregates. By implanting Z type aggregates the damage and failure of the concrete structure could be predicted accurately in this study. The results of this paper will help to promote further research and application of intelligent concrete.

The effect of humidity on the CO_2/N_2 separation performance of copolymers based on hard polyimide segments and soft polyether chains:Experimental and modeling

In this work, we studied two copolymers formed by segments of a rubbery polyether（PPO or PEO） and of a glassy polyimide（BPDA-ODA or BKDA-ODA） suitable for gas separation and CO2 capture. Firstly, we assessed the absorption of water vapor in the materials, as a function of relative humidity（R.H.）, finding that the humidity uptake of the copolymers lies between that of the corresponding pure homopolymers values.Furthermore, we studied the effect of humidity on CO2 and N2 permeability, as well as on CO2/N2 selectivity, up to R.H. of 75%. The permeability decreases with increasing humidity, while the ideal selectivity remains approximately constant in the entire range of water activity investigated. The humidity-induced decrease of permeability in the copolymers is much smaller than the one observed in polyimides such as Matrimid? confirming the positive effect of the polyether phase on the membrane performance.Finally, we modeled the humidity-induced decrease of gas solubility, diffusivity and, consequently, permeability, using a suitable approach that considers the free volume theory for diffusion and LF model for solubility. Such model allows estimating the extent of competition that the gases undergo with water during sorption in the membranes, as a function of the relative humidity, as well as the expected reduction of free volume by means of water molecules occupation and consequent reduction of diffusivity.

RARE EARTH CONTAINING POLYMER TERNARY COMPLEXES AND THEIR FLUORESCENT PROPERTIES

Rare earth containing fluorescence active polymer ternary complexes were synthesized and their absorption and emission properties were investigated.

EFFECT OF STRUCTURE OF FUNCTIONAL POLYMER ACTIVE MATERIALS ON PROPERTIES OF GADOLINIUM ION SELECTIVE ELECTRODE

In this paper,the functional polymeric active materials were prepared by the grafting copolymerization and their structure and properties were studied.The results show that the structure and properties of these ac- tive materials have the relative large effects on the properties of gadolinium ion selective electrodes.

STRUCTURE OF 1-BROMOMETHYL-7, 7-DIMETHYLBICYCLO[2.2.1]HEPT-2-YL ACRYLATE AND THE PROPERTIES OF ITS POLYMER

In this paper, the structure of 1-bromomethyl-7,7-dimethyl btcyclo[2.2.1]hept-2-yl acrylate has been studied by X-ray diffraction, and the relation between the molecular structure and the properties of polymerization and its polymer have been discussed.

Analysis on the Characteristic Properties of PEDOT Nano-particle Based on Reversed Micelle Method

Based on the study of a new type of conducting polymer poly （3,4-ethylenedioxythiophene） （PEDOT）,we focussed on the preparation and characteristics of PEDOT nanoparticles made by reversed micelle method.Moreover,we deeply investigated the optical,electrical and the thermal stability of PEDOT nanoparticles.The main results are as follows： the small-sized PEDOT nanoparticles were prepared and utilized by different methods,such as ultraviolet/visible （UV-Vis） spectroscopy,Fourier-transform infrared （FT- IR） spectrum,scanning electron microscopy（SEM） and so on.The results show that the amount of oxidizer,ultrasonic treatment,polymerizing temperature and doping degree can influent morphology,electrical ability and gas sensitivity of PEDOT nanoparticles.The Bragg peaks of nanoparticles at 6.7°,12.7°,25° were observed by XRD and the better orientation of molecular chain was attributed to the effective doping of toluene-p-sulfonic acid,which also resulted in an enhancement of thermal stability of nanoparticles than conventional PEDOT.

TWO DIMENSIONAL PROPERTIES OF REVERSED DUCKWEED AMPHIPHILIC POLYMER

The surface pressure-Area isotherms of Reversed Duckweed amphiphili polymer were examined in view of their chemical structure and two- dimentional properties of polymer monolayer were studied.

Effect of Reactive Nanoclays on Performances of PMMA/Reactive Nanoclay Nanocomposites

PMMA/reactive nanoclay nanocomposites were prepared by emulsion polymerization using two different reactive nanoclays. X-ray diffraction（XRD） and thermogravimetric analysis（TGA） results confirmed that the reactive nanoclays, kaolinite and montmorillonite, were obtained by the silylation reaction and the double bonds were grafted onto the edges and surfaces of the nanoclays. The presence of reactive nanoclays could increase the average molecular weights, the glass transition temperatures（Tg） and improve the thermal properties of nanocomposite. The tensile properties, Young＇s modulus, and the aging properties of the nanocomposite films were also enhanced while the light transmittance decreased. Furthermore, the nanocomposites with the reactive kaolinite presented better performances than that with the reactive montmorillonite. Finally, the action mechanism of the reactive nanoclays to the performances of PMMA/reactive nanoclay nanocomposites was proposed.

Poly(4,4＇-bis(thien-2-yl)azobenzene-co-3-hexylthiophene)： Synthesis and Optical/Electrochemical Properties

A conjugated polymer of poly（4,4＇-bis（thien-2-yl）azobenzene-co-3-hexylthiophene）（PTAB-H）, bearing azo group in main chain and soluble in THF, chloroform, was synthesized through FeCl3 oxidation copolymerization with 3-hexylthiophene, and the monomer of 4,4＇-bis（thien-2-yl）azobenzene was synthesized by Sandmeyer reaction and Suzuki reaction. The UV-Vis spectra of PTAB-H reveal that azo group in the main chain can extend the absorption and lower the band gap. The fluorescent spectra, photoluminescence（PL） spectra, cyclic voltammetry（CV） of PTAB-H were recorded.The gel permeation chromatography（GPC）, thermogravimetry analysis（TGA）, and differential scanning calorimetry（DSC） measurements indicated that the molecular weight Mn, Mw and polydispersity indices（PDI） of the polymer are 10876 g/mol, 22338 g/mol and 2.05 respectively and the temperature of 5% weight-loss is 224.6 ℃. No glass transition and crystallization melting peak was observed in the temperature range from 30 ℃ to 400 ℃.