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Structure and Luminescent Property of a New Cd(II) Coordination Polymer With (3,6)-Connected ant Topology 一种新型(3,6)连接蚂蚁结构的Cd(II)配位聚合物的结构和发光性能
Pub Date : 2016-05-24 DOI: 10.1080/15533174.2015.1136962
Zhuo-wen Fan, Long Li, K. Cui, Shuangbing Yang, Fusan Han
Solvothermal reactions of Cd(NO3)2, H3btc, and HBTA afforded a new Cd(II) compound, namely (NH3)2[Cd3(btc)2(BTA)(DMA)]n (1 H3btc = 1,3,5-benzenetricarboxylic acid, HBTA = 1,2,3- benzenetriazole, DMA = N, N′-dimethylacetamide). Single-crystal X-ray analysis reveals that 1 is a complicated three-dimensional (3D) framework based on benzotriazole-controlled trinuclear Cd(II) clusters, which can be simplified into a (3,6)-connected ant-type topological network. Moreover, the luminescent properties of this compound were also investigated at room temperature.
Cd(NO3)2、H3btc和HBTA的溶剂热反应生成新的Cd(II)化合物(NH3)2[Cd3(btc)2(BTA)(DMA)]n (1 H3btc = 1,3,5-苯三羧酸,HBTA = 1,2,3-苯三唑,DMA = n, n ' -二甲基乙酰胺)。单晶x射线分析表明,1是基于苯并三唑控制的三核Cd(II)团簇的复杂三维(3D)框架,可以简化为(3,6)连接的蚁型拓扑网络。此外,还研究了该化合物在室温下的发光性能。
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引用次数: 2
Gas Adsorption and Luminescent Properties of a Porous pcu-Type Zn(II) Coordination Polymer 一种多孔pcu型Zn(II)配位聚合物的气体吸附和发光性能
Pub Date : 2016-05-23 DOI: 10.1080/15533174.2015.1137061
Z. An, Jian Wang
A new Zn(II) compound, namely {Zn2(tdc)2(pi)}n (1 H2tdc = 2,5-thiophenedicarboxylic acid, pi = piperazine), has been synthesized via the solvothermal reactions of Zn(NO3)2·6H2O, H2tdc and pi. Single-crystal X-ray analysis reveals that compound 1 crystallizes in orthorhombic Pnma space group with cell parameters a = 20.734(6), b = 20.994(6), c = 18.539(6), and β = 90. The title compound features a three-dimensional (3D) pillar-layered framework. The gas adsorption and luminescent properties of 1 were investigated in the solid state at room temperature.
通过Zn(NO3)2·6H2O、H2tdc和pi的溶剂热反应,合成了新的Zn(II)化合物{Zn2(tdc)2(pi)}n (1 H2tdc = 2,5-噻吩二羧酸,pi =哌嗪)。单晶x射线分析表明,化合物1在正交Pnma空间群中结晶,晶胞参数a = 20.734(6), b = 20.994(6), c = 18.539(6), β = 90。标题化合物具有三维(3D)柱状分层框架。研究了1在室温下的固态气体吸附和发光性能。
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引用次数: 2
A New Mn(II) Coordination Polymer Based on Mixed 2-Aminoterephthalic Acid and 2,6-Bis(1-imdazoly)pyridine Ligands: Synthesis, Structure, and Luminescent Property 基于2-氨基对苯二甲酸和2,6-双(1-咪唑)吡啶的新型Mn(II)配位聚合物:合成、结构和发光性能
Pub Date : 2016-05-19 DOI: 10.1080/15533174.2015.1137072
Qifeng Liu, Wei Liu
A new Mn(II) coordination polymer, namely [Mn(impy)(NH2-pbc)]n (1 NH2-H2pbc = 2-aminoterephthalic acid, impy = 2,6-bis(1-imdazoly)pyridine), has been synthesized through solvothermal reactions of MnCl2, NH2-H2pbc and impy. Single X-ray structural analysis reveals that compound 1 features a 2D layered structure, and these 2D sheets are further stacked into a 3D supramolecular framework via weak van der Waals interactions. In addition, the luminescent properties of compound 1 and free impy ligand were also investigated at room temperature.
通过MnCl2、NH2-H2pbc和impy的溶剂热反应合成了一种新的Mn(II)配位聚合物[Mn(impy)(NH2-pbc)]n (1 NH2-H2pbc = 2-氨基对苯二甲酸,impy = 2,6-双(1-咪唑)吡啶)。单x射线结构分析表明,化合物1具有二维层状结构,这些二维层状结构通过弱范德华相互作用进一步堆叠成三维超分子框架。此外,还研究了化合物1和自由隐含配体在室温下的发光特性。
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引用次数: 2
Synthesis, Crystal Structure, and Thermal Analysis of a New Dy(III) Compound Based on Pyridinecarboxylate Ligand 一种新型吡啶羧酸配体Dy(III)化合物的合成、晶体结构和热分析
Pub Date : 2016-05-16 DOI: 10.1080/15533174.2015.1137066
Hui-min Liu
A new compound, namely [Dy4(L)6(H2O)4]n (1 H2L = 5-(pyridin-4-ylmethoxy)-isophthalic acid), has been hydrothermally synthesized and further characterized by the single-crystal X-ray diffraction, elemental analysis, infrared spectroscopy. Single-crystal X-ray diffraction analysis reveals that compound 1 crystallizes in monoclinic P21/n space group with a = 24.0566(5), b = 14.3950(3), c = 26.0162(6), and β = 92.146(2)°. In the compound, there are two different 1D chains constructed by L2− ligands and Dy(III) ions, which are further bridged by the L2− ligands into a complicated 3D framework.
用水热法合成了一个新化合物[Dy4(L)6(H2O)4]n (1 H2L = 5-(吡啶-4-基甲氧基)-间苯二甲酸),并用单晶x射线衍射、元素分析、红外光谱对其进行了表征。单晶x射线衍射分析表明,化合物1在单斜P21/n空间群中结晶,a = 24.0566(5), b = 14.3950(3), c = 26.0162(6), β = 92.146(2)°。在该化合物中,有由L2 -配体和Dy(III)离子构成的两个不同的1D链,它们被L2 -配体进一步桥接成一个复杂的3D框架。
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引用次数: 0
Development of New Fluorescent Dyes by Using Amine Modified Nanoparticles for Immunostaining 胺修饰纳米颗粒免疫染色荧光染料的研制
Pub Date : 2016-05-16 DOI: 10.1080/15533174.2015.1137062
E. Maltaş, Mustafa Ozmen, H. Ucan
Fluorescent labeling of DNA was studied by using two newly synthesized ligands, which are 4-(2-hydroxybenzylidinamino) benzoic acid (PHBA) and 4-(2-hydroxybenzylidinamino) phthalic acid (PHPA). Their binding capacity to calf-thymus DNA was determined on functionalized superparamagnetic iron oxide nanoparticles (SPIONs). 23.1 µg of DNA was immobilized on 25 mg of nanoparticles. Binding capacity of fluorescent ligands to DNA-APTS-SPIONs was also found as 2.36 µM for PHBA and 1.97 for PHPA at 25 mg of the nanoparticles. Binding of the DNA to the ligands were examined by scanning electron microscopy, transmission electron microscopy, infrared spectroscopy, and confocal microscopy.
采用新合成的4-(2-羟基苄基氨基)苯甲酸(PHBA)和4-(2-羟基苄基氨基)邻苯二甲酸(PHPA)两种配体对DNA的荧光标记进行了研究。在功能化的超顺磁性氧化铁纳米颗粒(SPIONs)上测定了它们与小牛胸腺DNA的结合能力。23.1µg DNA固定在25mg纳米颗粒上。荧光配体与DNA-APTS-SPIONs的结合能力在25 mg时,PHBA和PHPA的结合能力分别为2.36µM和1.97µM。通过扫描电子显微镜、透射电子显微镜、红外光谱和共聚焦显微镜检查DNA与配体的结合。
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引用次数: 0
UV-Assisted Synthesis of White Emissive CdS Nanocrystals at Room Temperature 室温下紫外辅助合成白光发光CdS纳米晶体
Pub Date : 2016-05-16 DOI: 10.1080/15533174.2015.1137063
M. Molaei, S. Salehi, M. Karimipour
In this work CdS nanocrystals (NCs) were synthesized by a simple UV-assisted method. Prepared NCs were characterized by means of XRD, FTIR, TEM, UV-vis, and PL analyses. Synthesized NCs was in hexagonal phase with an average size about 3.5 nm. The NCs bandgap shorten from 3.6 to 3.2 eV only by increasing the illumination from 3 to 12 min. PL spectra showed a white emission and PL peak shifted from near 518 nm to 540 nm by increasing illumination time from 3 to 12 min.
本文采用一种简单的紫外辅助法制备了CdS纳米晶体。采用XRD、FTIR、TEM、UV-vis、PL等方法对制备的纳米碳纳米管进行了表征。合成的纳米颗粒呈六方相,平均尺寸约为3.5 nm。当光照时间从3分钟增加到12分钟时,NCs带隙从3.6 eV缩短到3.2 eV。当光照时间从3分钟增加到12分钟时,PL光谱呈现白色发射,PL峰从518 nm附近移到540 nm附近。
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引用次数: 1
A New Trinodal (3,4,6)-Connected Ni(II) Coordination Polymer Based on the Mixed Ligands of 6-(3′,4′-Dicarboxyl-Phenoxy) Isophthalic Acid and 4,4′-Bipyridine 基于6-(3′,4′-二羧基-苯氧基)间苯二甲酸和4,4′-联吡啶混合配体的新型三节(3,4,6)连接镍(II)配位聚合物
Pub Date : 2016-05-16 DOI: 10.1080/15533174.2015.1137064
C. Song, Xiaohui Li, Wei Liu, Ziqing Cao, Yuanyuan Ren, Qichao Zhou, Li Zhang
Reported here is a new Ni(II) compound, namely {Ni2(L)(bipy)2(H2O)2}n (1 H4L = 6-(3′,4′-dicarboxyl-phenoxy)isophthalic acid, bipy = 4,4′-bipyridine), which has been synthesized via the solvothermal reactions of Ni(NO3)2·6H2O, H4L and bipy. Single crystal X-ray analysis reveals that compound 1 crystallizes in triclinic P-1 space group with cell parameters a = 9.8887(6), b = 9.9884(4), c = 19.2310(11), α = 79.187(4), β = 83.862(5), γ = 80.708(4). The title compound features a three-dimensional (3D) framework and can be simplified into a trinodal (3,4,6)-connected topological network. Moreover, the thermal and luminescent properties of compound 1 were also investigated.
本文报道了一种新的Ni(II)化合物{Ni2(L)(bipy)2(H2O)2}n (1h4l = 6-(3′,4′-二羧基-苯氧基)间苯二甲酸,bipy = 4,4′-联吡啶),通过Ni(NO3)2·6H2O、H4L和bipy的溶剂热反应合成。单晶x射线分析表明,化合物1在三斜P-1空间群中结晶,胞元参数为a = 9.8887(6), b = 9.9884(4), c = 19.2310(11), α = 79.187(4), β = 83.862(5), γ = 80.708(4)。标题化合物具有三维(3D)框架,可简化为三节(3,4,6)连接的拓扑网络。此外,还研究了化合物1的热性能和发光性能。
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引用次数: 1
Syntheses, Characterization, and Crystal Structures of Schiff Base Zinc(II) Complexes With Tetrahedral Coordination 具有四面体配位的席夫碱锌(II)配合物的合成、表征和晶体结构
Pub Date : 2016-05-16 DOI: 10.1080/15533174.2015.1137065
J. Qin, Z. Xia, Yu Zhang, F. Niu, Z. You, Hailiang Zhu
Two new mononuclear Schiff base zinc(II) complexes, [ZnClL1(N3)]·2MeOH (1) and [ZnBr2(L2)]·MeOH (2) (L1 = 4-methyl-2-[(2-piperazinium-1-ylethylimino)methyl]phenolate; L2 = 2-[(2-diethylammonioethylimino)methyl]-4-methylphenolate), have been prepared and characterized by elemental analyses, infrared and UV-vis spectroscopy, and single-cyrstal X-ray diffraction. Complex 1 crystallizes in the orthorhombic space group Pbca with unit cell dimensions a = 18.703(1), b = 11.8643(6), c = 19.081(1) Å, V = 4234.0(4) Å3, Z = 8, R1 = 0.0475, and wR2 = 0.1046. Complex 2 crystallizes in the orthorhombic space group P212121 with unit cell dimensions a = 8.863(2), b = 13.360(2), c = 17.066(3) Å, V = 2020.7(7) Å3, Z = 4, R1 = 0.0803, and wR2 = 0.1859. The Zn atoms in the complexes are four-coordinated in tetrahedral geometry by the phenolate O and imine N atoms of the Schiff base ligands, and two halide or pseudohalide ligands. Crystals of the complexes are stabilized by hydrogen bonds.
两个新的单核希夫碱锌(II)配合物,[ZnClL1(N3)]·2MeOH(1)和[ZnBr2(L2)]·MeOH (2) (L1 = 4-甲基-2-[(2-哌嗪-1-基乙基)甲基]酚酸盐;合成了L2 = 2-[(2-二乙基氨基乙基)甲基]-4-甲基苯酚),并通过元素分析、红外、紫外-可见光谱和单晶x射线衍射对其进行了表征。配合物1在正交空间群Pbca中结晶,晶胞尺寸a = 18.703(1), b = 11.8643(6), c = 19.081(1) Å, V = 4234.0(4) Å3, Z = 8, R1 = 0.0475, wR2 = 0.1046。配合物2在正交空间群P212121中结晶,晶胞尺寸a = 8.863(2), b = 13.360(2), c = 17.066(3) Å, V = 2020.7(7) Å3, Z = 4, R1 = 0.0803, wR2 = 0.1859。配合物中的Zn原子与席夫碱配体中的酚O和亚胺N原子以及两个卤化物或假卤化物配体呈四面体四配位。配合物的晶体由氢键稳定。
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引用次数: 3
Manganese(III) Tetraphenylporphyrin Encapsulated by Ion-Modified Hexagonal Mesoporous Silica With Unexpected Enhanced Epoxidation Selectivity 离子修饰六方介孔二氧化硅包封的四苯基卟啉锰具有意想不到的增强环氧化选择性
Pub Date : 2016-05-16 DOI: 10.1080/15533174.2015.1137059
Weijie Zhang, P. Jiang, Ying Wang, Jian Zhang, Pingbo Zhang
Tetraphenylporphyrin manganese (III) chloride (Mn-TPP) was encapsulated into hexagonal mesoporous silica (HMS) modified by different Lewis acid ions Al, Ti, Zr, and W, which have been tested for selective oxidation of unsaturated olefins and more challenged fatty acid esters under mild condition. Pure W-HMS support displayed no epoxidation activity under the present condition; nonetheless, an unexpected enhanced selectivity for Mn-TPP/W-HMS (90%) with respect to the other samples, especially to homogenous Mn-TPP, indicated the promoted role of W ions over the support. In addition, TG analysis and wetting contact angle measurement were determined in order to reveal the hydrophobic nature of heterogeneous materials, which has been preliminarily scrutinized as the factor influencing catalytic selectivity. That is, Mn-TPP/W-HMS exhibited around 90% selectivity because of a better hydrophobic nature.
将四苯基卟啉锰(III)氯(Mn-TPP)包裹在六方介孔二氧化硅(HMS)中,通过不同的Lewis酸离子Al、Ti、Zr和W修饰,在温和条件下对不饱和烯烃和更具挑战性的脂肪酸酯进行了选择性氧化试验。在此条件下,纯W-HMS载体无环氧化活性;然而,相对于其他样品,Mn-TPP/W- hms的选择性出乎意料地提高(90%),特别是对均质Mn-TPP,表明W离子的促进作用超过了载体。此外,通过TG分析和润湿接触角测量,揭示了非均相材料的疏水性质,初步探讨了疏水性质是影响催化选择性的因素。即Mn-TPP/W-HMS由于具有较好的疏水性,表现出90%左右的选择性。
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引用次数: 1
Synthesis of Ag Porous Carbon Nanofiber by Electrospinning and Their Use as Catalyst for Styrene Epoxidation 静电纺丝法合成银多孔碳纳米纤维及其在苯乙烯环氧化反应中的催化作用
Pub Date : 2016-05-16 DOI: 10.1080/15533174.2015.1137067
Qi Wang, Chunping Li, J. Bai, Junzhong Wang
A simple method to prepare the Ag porous carbon nanofiber is reported. Ag porous carbon nanofiber was prepared by electrospinning and high temperature calcination. In this process, AgNO3-PMMA/PAN solution was the precursor solution of electrospinning, and Ag nanoparticles and pores were made by high temperature calcination. The catalytic activity of the Ag porous carbon nanofibers was confirmed by the styrene epoxidation. In the catalytic process, the conversation of styrene was 71% and the selectivity of styrene oxide was 83%.
报道了一种制备银多孔碳纳米纤维的简单方法。采用静电纺丝和高温煅烧法制备了银多孔碳纳米纤维。该工艺以AgNO3-PMMA/PAN溶液为静电纺丝的前驱体溶液,通过高温煅烧制备银纳米颗粒和孔。通过苯乙烯环氧化反应证实了银多孔碳纳米纤维的催化活性。在催化过程中,苯乙烯的转化率为71%,苯乙烯氧化物的选择性为83%。
{"title":"Synthesis of Ag Porous Carbon Nanofiber by Electrospinning and Their Use as Catalyst for Styrene Epoxidation","authors":"Qi Wang, Chunping Li, J. Bai, Junzhong Wang","doi":"10.1080/15533174.2015.1137067","DOIUrl":"https://doi.org/10.1080/15533174.2015.1137067","url":null,"abstract":"A simple method to prepare the Ag porous carbon nanofiber is reported. Ag porous carbon nanofiber was prepared by electrospinning and high temperature calcination. In this process, AgNO3-PMMA/PAN solution was the precursor solution of electrospinning, and Ag nanoparticles and pores were made by high temperature calcination. The catalytic activity of the Ag porous carbon nanofibers was confirmed by the styrene epoxidation. In the catalytic process, the conversation of styrene was 71% and the selectivity of styrene oxide was 83%.","PeriodicalId":22118,"journal":{"name":"Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87094183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
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Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry
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