A New Dinuclear Zinc Polymer Based on 3-Methoxy-2-hydroxybenzaldehyde:Synthesis,Structure,Spectral Characterization and Hirshfeld Surface Analysis

A highly efficient fluorescence material dinuclear zinc polymer [Zn2（mhbd）2（dca）2]n （1, Hmhbd is 3-methoxy-2-hydroxybenzaldehyde, dca is N（CN）2？） has been synthesized under room temperature and structurally characterized by elemental analysis, IR, and single-crystal X-ray diffraction. The structure belongs to the triclinic system, space group P with a = 8.475（1）, b = 9.595（1）, c = 15.001（1） A, α = 86.84（1）, β = 81.10（1）, γ = 68.78（1）°, Mr = 565.15, V = 1123.5（1） ？3, Dc = 1.671 g？cm–3, F（000） = 568, μ = 2.185 mm–1, R = 0.0451, and wR = 0.1297. 1 is a dinuclear zinc complex which further constructs a 1D chain through double μ1,5-dca bridge. Luminescent property and Hirshfeld surface analysis of 1 have been studied. The result indicates that the fluorescence intensity of complex 1 is forty-one times the fluorescence intensity of Hmhbd ligand.

A New 2D Zinc(Ⅱ) Coordination Polymer Constructed by Imidazole-4,5-dicarboxylic Acid(H_3IDC) and 1,4-Bis(imidazol-1-ylmethyl)-benzene(bix)

A new 2D Zn（Ⅱ） coordination polymer [Zn（HIDC）（bix）0.5]n（1） was obtained by the hydrothermal reaction of ZnCl2,imidazole-4,5-dicarboxylic acid（H3IDC） and 1,4-bis（imidazol-1-ylmethyl）-benzene（bix） with a 2：2：1 mole ratio.X-ray diffraction crystal structural analysis reveals it crystallizes in monoclinic,space group P21/n with a = 12.125（3）,b = 10.541（3）,c = 12.484（3） ,β = 115.834（4）°,V = 1436.0（6） 3,Mr = 338.60,Z = 4,Dc = 1.566 Mg·m-3,F（000） = 684,μ（MoKα） = 1.730 mm-1,the final R = 0.0439 and wR = 0.0888 for 2101 observed reflections with I ≥ 2σ（I）.In 1,each zinc（Ⅱ） ion is five-coordinated with a slightly distorted trigonal bipy-ramidal coordination geometry,and each μ2-HIDC2-acts as a bridge to bond two neighboring Zn（Ⅱ） ions,leading to a 1D zigzag chain architecture.The adjacent zigzag chains are further linked by μ2-bix to form an infinite 2D network structure.The fluorescence spectrum of 1 exhibits intense emission at 466 nm when excited at 397 nm in solid state at room temperature.

A New 1D Zinc Coordination Polymer Constructed by 1-Naphthylacetate and 4,4'-bpy:Synthesis,Structure and Luminescent Property

One new zinc coordination polymer,[Zn（NAA）2（4,4＇-bpy）]n（1,HNAA = 1-naphthaleneacetic acid,4,4＇-bpy = 4,4＇-bipyridine）,has been synthesized under hydrothermal conditions and characterized by elemental analysis,IR spectroscopy,thermogravimetric analysis（TGA）,and single-crystal X-ray diffraction.Coordination polymer 1 is of monoclinic system,space group Cc with a = 9.8720（6）,b = 16.7397（9）,c = 17.0371（12） ,β = 104.8080（10）°,V = 2721.9（3）3,C34H26N2O4Zn,Z = 4,Mr = 591.94,Dc = 1.444 g/cm3,μ（MoKα） = 0.946 mm-1,F（000） = 1224,the final R = 0.0282 and wR = 0.0720 for 3300 observed reflections with I 〉 2σ（I）.1 exhibits an interesting one-dimensional chain structure.Furthermore,the luminescent property of 1 has also been investigated.

A Two-dimensional Anthracene-9,10-dicarboxylate Zinc(Ⅱ) Coordination Polymer Based on Binuclear [Zn_2Cl_2] Nodes: Synthesis, Characterization and Luminescent Properties

A two-dimensional（2D） 44 topological ZnⅡ coordination polymer {[Zn2Cl2（L）（4bpy）2]}∞（H2L = anthracene-9,10-dicarboxylic acid, 4bpy = 4,4ˊ-bipyridine） based on binuclear [Zn2Cl2] nodes has been synthesized and characterized by IR, elemental analysis, X-ray powder diffraction and single-crystal X-ray diffraction analysis. Moreover, the luminescent properties of the correspon- ding compound have been briefly investigated.

Hydrothermal Synthesis and Crystal Structure of a New 2D Zinc(Ⅱ) Coordination Polymer with 2-Aminoethanesulfonic Acid

A new 2D Zn（Ⅱ） coordination polymer [Zn（TAU）2]n （1, HTAU=2-aminoethane- sulfonic acid） constructed by 2-aminoethanesulfonic acid ligand has been hydrothermally synthesized by the reaction of Zn（CH3COO）2 and 2-aminoethanesulfonic acid with a 1：2 mole ratio and characterized by single-crystal X-ray diffraction, elemental analysis, infrared spectroscopy and thermogravimetric analysis. Crystal structural analysis reveals it crystallizes in monoclinic, space group P21/c with a=8.672（4）, b=6.523（3）, c=9.134（5） , β=115.441（5）°, V=466.6（4） 3, Mr=313.65, Z=2, Dc=2.232 Mg·m-3, F（000） =320, μ（MoKα）=3.091 mm-1, the final R=0.0358 and wR=0.0919 for 2026 observed reflections with Ⅰ 〉 2σ（Ⅰ）. In the structure, each zinc（Ⅱ） ion is coordinated in a slightly distorted octahedron, and each μ3-TAU– acts as a bridge to bond three neighboring Zn（Ⅱ） ions to form an infinite 2D network structure.

Synthesis and Crystal Structure of a 1D Alternate Chain Polymer [Zn_2(NBA)_2(4,4'-bipy)]_n

A one-dimensional zinc-containing coordination polymer, [Zn2（NBA）2（4,4′-bipy）]n （NBA = 3-nitrobenzoic acid, 4,4′-bipy = 4,4′-bipyrindine）, has been solvothermally synthesized and characterized by single-crystal X-ray diffraction, IR and elemental analysis. The crystal structure is of monoclinic, space group C2/c with a = 24.6478（2）, b = 14.0964（3）, c = 11.4275（2）A, β=108.7870（10）°, V = 3758.89（11） ,A^3, C38H20N6O16Zn2, Mr = 947.34, Z = 4, De = 1.674 g/cm^3 μ= 1.363 mml, F（000） = 1912, R = 0.0720 and wR = 0.2277 for 2841 observed reflections （I 〉 2σ（I）. In this compound, NBA in syn-syn coordination mode bridges zinc centers into dimericzinctetracarboxylate [Zn2（COO）4] secondary building units （SBUs） which are linked through μ-4,4′-bpy affording 1D alternating chains. These adjacent chains are further stacked through intermolecular π...π interactions to form a 3D framework.

Synthesis and Crystal Structure of a New One-dimensional Double Helical-chain Polymer, {Zn(O_2CC_(12)H_8CO_2)(H_2O)}_n

A new zinc polymer, {Zn（O2CC12H8CO2）（H2O）}, or {Zn（DPHA）（H2O）}n （O2CC12H8CO2, DPHA = 1,1′ -biphenyl-2,2′-dicarboxylate dianion） has been synthesized under hydrothermal conditions. The crystal is of monoclinic, space group P21/c with a = 12.8418（5）, b = 5.9505（2）, c = 17.2989（5） A, β = 104.020（2）°, V = 1282.52（8） A^3, C14H10O5Zn, Mr= 323.61, Z = 4, Dc = 1.676 g/cm^3,μ = 1.930 mm^-1, F（000） = 656, R = 0.0766 and wR = 0.1871 for 1775 observed reflections （I 〉 2σ（I））. It consists of Zn2（DPHA）2（H2O）2 units, which are further extended into a one-dimensional double helical-chain polymer via Zn-O bonding. The hydrogen bonding interactions extend the helical chains into a two-dimensional layer structure.

Synthesis, Structure and Luminescent Property of a New Zn(Ⅱ) Coordination Polymer Based on 1,3,5-Benzenetricarboxylate and 4,4'-Bipyridine Ligands

A new Zn（II） coordination polymer [Zn3（BTC）2（4,4＇-bpy）（CO）2]n （1, H3BTC = 1,3,5-benzenetricarboxylic acid, 4,4＇-bpy = 4,4＇-bipyridine） has been prepared through urothermal reaction of zinc nitrate hexahydrate with 1,3,5-benzenetricarboxylic acid and 4,4＇-bipyridine, and characterized by elemental analysis, IR spectroscopy, TGA and powder XRD, and its crystal structure was determined by single-crystal X-ray diffraction analysis. The title compound crystallizes in the monoclinic system, space group C2/c, with a = 10.262（3）, b = 18.838（5）, c = 15.083（4）/k, fl = 99.203（4）°, V = 2878.3（14） A3, C30H14Zn3N2O14, Mr= 822.54, Z = 4, Dc = 1.898 g/cm3,μ = 2.561 mm-1,F（000） = 1640, R = 0.0363 and wR = 0.0932 for 2828 observed reflections （I 〉 2σ（I））. X-ray analysis shows that the asymmetric unit of the title compound contains two crystallographically unique Zn（lI） atoms which are connected by BTC3- ligands and 4,4＇-bpy coligands to form a 3D framework with 1D channels. The solid luminescence of ligand and the title complex was also studied at room temperature.

Ionothermal Synthesis and Characterization of a Threedimensional Anionic Zinc-5-sulfoisophthalate Framework Charge-balanced with the 1-Ethyl-3-methylimidazolium

The ionothermal reaction of Zn（NO3）2·6H2O with 5-sulfoisophthalic acid monosodium salt（NaH2SIP） and 1,2,4-triazole in 1-ethyl-3-methylimidazolium tetrafluoroborate（EMIM-BF4） ionic liquid has afforded the compound {（EMIM）[Zn（SIP）]}n（1）.The Zn（Ⅱ） ions are linked by the carboxylate groups of SIP^3- ligands to give a two-dimensional layered structure featuring the centrosymmetric dinuclear Zn2（μ2-COO）2 units.The adjacent two-dimensional layers are further linked by the Zn-0 bonds between the Zn（Ⅱ） ions and the sulfonate O atoms to generate a three-dimensional anionic[Zn（SIP）]n^n- framework featuring one-dimensional open channels propagating along the a axis.The imidazolium cations[EMIM]^＋ derived from ionic liquid act as extraframework charge-balancing species for the anionic[Zn（SIP）]n^n- framework and occupy the void space of the one-dimensional open channels.The rich ionic environments of the ionic liquid may be particularly helpful in the formation of the ionic compound 1.The roles of the ionic liquid in ionothermal synthesis and crystallization of the compound are briefly discussed.Furthermore,compound 1 displays a photoluminescent emission at 490 nm upon excitation at 406 nm.

Two Metal-organic Coordination Polymers with Rigid Bis(triazole) Ligand： Assembly, Structures, and Fluorescence Properties

Two new coordination polymers containing rigid bis（triazole）, namely, [Ni（btb）_（0.5）（nph）（H_2O）]_n（1） and [Zn（btb）（SO_4）]_n（2）（btb = 4,4a-bis（1,2,4-triazolyl-1-yl）-biphenyl, H_2nph = 3-nitrophthalic acid） have been synthesized and characterized by elemental analysis, IR spectra, and single-crystal X-ray diffraction. Complex 1 shows a 3D trinodal（3,4,4）-connected sqc69 topology. Complex 2 presents a 2D uninodal 4-connected sql network, which is further packed into a 3D supramolecular framework by C-H···O hydrogen bonds. Thermal stabilities and fluorescence properties of two complexes have been discussed in detail.

Zinc Complexes of New Chiral Aminophenolate Ligands: Synthesis, Characterization and Reactivity toward Lactide

The syntheses of a library of new chiral aminophenolate bidentate O,N-type ligands HOC6H4(2-R- 4-R′)CH2N(Me)CH(Me)C6H5 [R = R′ = But, 1;R = R′ = Pent, 2;R = But, R′ = Me, 3;R = Me, R′ = But, 4;R = R′ = Me, 5] and tridentate O,N,O-type ligands HOC6H4(2,4-But)CH = NCH(R′′)C6H5 [R′′ = Me, 6;R′′ = CH2OMe, 7] are reported. These ligands were characterized by elemental analysis, nuclear magnetic resonance spectroscopy (1H & 13C), and single crystal X-ray diffraction. These ligands serve as chiral auxiliaries for inorganic chemists to design chiral metal-based complexes for asymmetric catalysis and stereoselective polymerization reactions. Three new heteroleptic zinc complexes based on these ligands have been synthesized in moderate yields via a ligand-exchange transamination reaction between homoleptic [Zn(N(SiMe3)2)2] and one equivalent of corresponding ligands to afford [L3ZnN- (SiMe3)2] (3a), [L4ZnN(SiMe3)2] (4a), and [L7ZnN(SiMe3)2] (7a). Solvent-free polymerization of raclactide at 130°C using these zinc compounds yielded atactic polylactides with Mw 10,000 g/mol and narrow polydispersity of 1.3.

Syntheses, Structures, and Luminescent Properties of the ZnⅡ and CdⅡ 1-D Chain Polymers Assembled by Salicylhydroxamic Acid

TWO complexes of compositions [Zn（H2shi）（CHsCOO）]. （1） and [Cd（H2shih（H20）]. （2） （H3shi = salicylhydroxamic acid） have been prepared under solvothermal conditions. They are characterized by X-ray single-crystal diffraction, IR and elemental analysis. The crystal of 1 belongs to the tetragonal system, space group I41/a with a = 18.972（3）, b = 18.972（3）, c = 10.938（2） A, V= 3937.1（I） A3, C9H9NOsZn, Mr - 276.54, Z = 16, Dc = 1.866 g/cm3,μ = 2.500 mm-1, F（000） = 2240, the final R = 0.0425 and wR = 0.123. The crystal of 2 belongs to the monoclinic system, space group P2/c with a = 16.647（3）, b = 6.4577（I）, c = 6.5623（I） A, V = 702.4（2） A3, C14H4Cd2N2OT, Mr = 434.68, Z = 2, Dc = 2.055 g/cm3,μ = 1.599 mm-1, F（000） = 432, the final R = 0.0211 and wR = 0.0761. They both possess I-D polymeric chain structures. The luminescent properties of complexes I and 2 have been investigated.

Batch Studies for Sorption of Ga(III), Cu(II), Ni(II) and Zn(II) Ions onto Synthetic Polymeric Resins

Poly(acrylamide-acrylic acid-dimethyl amino ethylmethacrylate), p(AM-AA-DMAEM) and Poly(acrylamide-acrylic acid)-ethylene diamine tetracetic acid disodium, p(AM-AA)-EDTANa2 were prepared by gamma radiation-induced template polymerization technique. The prepared polymeric materials were used for the sorption of Ga(III), Cu(II), Ni(II) and Zn(II) in aqueous solution. The effect of pH, weight of resins, metal ion concentrations and contact time on the sorption of these metal ions were studied.

2-((2,6-二甲基苯基)氨基)乙醇铝和锌配合物的合成、结构及催化活性

研究了AlMe_(3)和ZnEt_(2)与ArNHCH_(2)CH_(2)OH(HL,Ar=2,6-Me_(2)C_(6)H_(3))的反应,合成了一个双核铝配合物[(Me_(2)Al)(L)]_(2)(1)及一个四核锌配合物[EtZn_(2)(L)_(3)]_(2)(2)。通过核磁、元素分析及单晶X射线衍射分析,对化合物1和2进行了详细的结构表征。结果表明,配合物1在固态下是一个中心对称的具有Al_(2)O_(2)骨架的二聚体,而配合物2存在一个Zn_(4)O_(6)核,其可被视为缺少一对相反顶点的2个并排立方体结构。初步的催化活性测试表明,铝配合物1对ε-己内酯的开环聚合反应没有催化活性,但锌配合物2却表现出很好的催化活性,且能很好地控制所得聚合物的分子量分布在较窄的范围。

纤维素纳米纤维PAM基混合凝胶对柔性锌空气电池的性能影响

采用自由基聚合法制备具有良好柔性的聚丙烯酰胺(PAM)基凝胶电解质,作为柔性锌空气电池电解质。探究了不同含量的纤维素纳米纤维(CNF)对PAM基凝胶电解质表面形貌、离子电导率、吸液率、保水率等一系列性能的影响,并将含有不同含量CNF的PAM基凝胶电解质组装成锌空气电池,分别对其进行了电化学阻抗、功率密度、恒流放电、放电倍率、充放电循环等电化学性能测试。结果表明:所制纤维素纳米纤维PAM基混合凝胶电解质(PAMC)(以5%含量CNF的PAMC凝胶电解质为例)具有较高的吸液率(4383%)、保水率(79.00%)和离子电导率(340mS/cm),组装的柔性锌空气电池功率密度为19.03mW/cm^(2),在低电流密度和高电流密度(0.25~11mA/cm^(2))下都有较好的放电性能,且稳定性较好,并可连续充放电23.74h,循环效率为57.5%。

氧化锌/聚吡咯复合材料制备及其电化学传感性能

利用水热法制得氧化锌纳米阵列作为形貌导向的模板,在ITO导电玻璃上制备氧化锌纳米棒,再利用电化学法成功合成氧化锌/聚吡咯膜,该复合材料制得的电极比未使用氧化锌阵列制备的电极要灵敏。对合成的氧化锌/聚吡咯膜进行表征、电化学性能测试。得到如下结论:氧化锌/聚吡咯复合材料形貌成网状致密结构;合成电位对制备氧化锌/聚吡咯的影响较大,当用恒电位法聚合吡咯时,其适宜的电位是0.8~1.0 V左右;当循环伏安法测电化学传感性能时,最佳扫描速度为0.5 V/s;氧化锌/聚吡咯复合材料对过氧化氢具有较高的催化还原功能,因此氧化锌/聚吡咯复合材料可做传感器具有更高的灵敏度。

酰胺基官能化氮杂环卡宾锌配合物的合成、表征及催化性能探究

通过溶剂热法,使双齿酰胺基官能化氮杂环卡宾(NHC)配体与ZnCl2反应,合成了一种全新的酰胺基官能化N-杂环卡宾锌配合物L1-Zn。通过单晶X射线衍射(SC-XRD)、红外光谱(FTIR)和能谱(EDX)对其结构和化学组成进行了表征。锌配合物的晶体结构测定揭示了其为零维结构。该配合物可催化丙交酯开环聚合反应,在无溶剂条件下,当反应温度120℃、反应时间3 h、单体与催化剂物质的量比100∶1时,丙交酯的转化率为21%。

原位聚合氧化锌抗菌聚酯纺丝工艺探讨

以自制的原位聚合氧化锌抗菌聚酯切片为原料,合理选择干燥条件、纺丝工艺,生产135 dtex/72 f聚酯纤维,考察原位聚合氧化锌抗菌聚酯的纺丝状况及纤维性能。结果表明:选择原位抗菌切片干燥温度150℃,干燥时间24 h,纺丝温度287~289℃,卷绕速度2 700 m/min,生产的原位抗菌聚酯预取向丝(POY)断裂强度较好,大于2.4 c N/dtex;对POY进行加弹处理,控制假捻变形速度600 m/min,拉伸比1.72,第一热箱温度180℃,第二热箱温度165℃,生产的抗菌拉伸变形丝的卷曲收缩率和稳定度均较好,断裂强度大于3.6 cN/dtex;所织造的抗菌织物对大肠埃希菌、金黄葡萄球菌、白念珠菌的抑菌率均达94%以上。

连续管式工艺生产二氧化碳基聚碳酸酯聚醚多元醇研究

连续管式工艺适合工业化生产二氧化碳基聚碳酸酯聚醚多元醇,通过与间歇釜式工艺对比,发现在相同的保留时间情况下,连续管式工艺的反应体系环氧丙烷转化率更高,聚碳酸酯链节高于58%,多元醇产物的选择性更高,且不同批次产品在投料相同的情况下稳定性较好,分子量分布指数低于1.62,适用于胶粘剂、水性乳液等各类聚氨酯产品。