Effects of Metal Ions and N-Donor Ligands with Different Coordination Characters on the Construction of d10 Metal-organic Complexes with Selective Photocatalytic Activities

2014 ◽  
Vol 69 (6) ◽  
pp. 681-690
Author(s):  
Guo-Cheng Liu ◽  
Nai-Li Chen ◽  
Ju-Wen Zhang ◽  
Yun Qu ◽  
Hong-Yan Lin ◽  
...  
Keyword(s):  
Metal Ions ◽  
Donor Ligands ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
Organic Complexes ◽  
D10 Metal ◽  
Photocatalytic Activities ◽  
Metal Organic ◽  
Supramolecular Networks

Four new d10 metal-organic coordination polymers, [Zn(L)(phen)(H2O)] (1), [Cd(L)(phen)] (2), [Zn(L)(bppdc)]·3H2O (3), and [Cd(L)(bppdc)]·3H2O (4) [L=2-carboxymethylsulfanyl nicotinic acid, phen=1,10-phenanthroline, bppdc=N;N`-bis(pyridin-3-yl)pyridine-2,6-dicarboxamide], have been obtained from hydrothermal reactions of zinc(II)=cadmium(II) nitrates with the semi-rigid N-= S-containing dicarboxylate L, and the two structurally disparate neutral N-donor ligands phen and bppdc. Single-crystal X-ray diffraction analysis has revealed that compound 1 is a one-dimensional (1- D) helical coordination polymer linked by ZnII atoms and L spacers. Compound 2 features a doublechain structure connected via binuclear CdII units and pairs of L linkers. Adjacent chains of 1 and 2 are packed into 3-D supramolecular networks by hydrogen bonds and p-p stacking interactions. Compounds 3 and 4 exhibit similar 2-D (4,4)-connected wave-like networks based on linear [M-L]n and zigzag [M-bppdc]n metal-organic chains (M=ZnII for 3 and CdII for 4). The effects of metal ions and N-donor ligands with different coordination characters are discussed. Moreover, the photoluminescence properties and photocatalytic activities of compounds 1 - 4 were investigated.

A New Organic-Inorganic Hybrid Based on L-Arginine and Polyoxoanion

2015 ◽  
Vol 1105 ◽  
pp. 335-338
Author(s):  
Qiong Wu ◽  
Jing Lu ◽  
Xiao Lin Ji ◽  
Tao Yu Zou ◽  
Zhen Fang Qiao ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Sodium Cation ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Inorganic Hybrid ◽  
X Ray ◽  
Hydrogen Bonding Interactions ◽  
Photocatalytic Activities ◽  
Metal Organic ◽  
Supramolecular Networks

Modifying polyoxometalates with organic and/or metal-organic moieties is a widely adopted method for broading the range of properties. In this work a new polyoxometalate constructed from Anderson-type polyoxoanions and L-arginine (Arg =L-arginine) molecules Na [CrMo6(OH)6O18]}(H2Arg)2·8H2O(1) has been synthesized via conventional method and characterized by routine techniques. Single-crystal X-Ray diffraction analysis shows that compound 1 is constructed by chiralL-arginine grafted Anderson-type clusters, sodium cation and water molecules which are further stabilized by hydrogen bonding interactions constitute 3D supramolecular networks. In addition, both antitumor behavior and photocatalytic activities of compound 1 were investigated.

Two 3D ZnII Metal–Organic Frameworks with 3- and 8-Fold Interpenetration: Syntheses, Structures, Photodegradation, and Photoluminescent Properties

2017 ◽  
Vol 70 (3) ◽  
pp. 314 ◽  
Author(s):  
Chuan-Bin Fan ◽  
Xiang-Min Meng ◽  
Yu-Hua Fan ◽  
Zi-Ao Zong ◽  
Xiao-Yin Zhang ◽  
...  
Keyword(s):  
Single Crystal ◽  
Metal Organic Frameworks ◽  
Xrd Analysis ◽  
Donor Ligands ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metal Organic ◽  
Solvothermal Conditions ◽  
Single Crystal Xrd Analysis

Two novel coordination polymers, namely {[Zn(sbdc)(bmib)]·0.4H2O}n (1) and {[Zn(sbdc)(bibd)]·DMF}n (2) (H2sbdc = 4,4′-stilbenedicarboxylic, bmib = 1,4-bis(2-methylimidazol-1-yl)butane, bibd = 1,1′-(1,4-butanediyl)bis(imidazole), DMF = N,N-dimethylformamide), have been acquired under solvothermal conditions, and have been characterised by elemental analysis, infrared spectra, thermogravimetric analysis, and single-crystal X-ray diffraction (XRD). Single-crystal XRD analysis reveals that 1 shows eight-fold interpenetrating 3D frameworks with a four-connected (66) sqc6 topology and 2 displays four-connected three-fold interpenetrating 3D frameworks. The flexible N-donor ligands play an important role in the construction of the final topological structures for 1 and 2. Furthermore, 1 and 2 exhibit good photodegradation capability and photoluminescence properties.

Synthesis, structure, and fluorescence properties of two metal-organic complexes based on a tripodal carboxamide-containing ligand

2020 ◽  
Vol 44 (7-8) ◽  
pp. 453-459
Author(s):  
Yan Wang ◽  
Xiner Xu ◽  
Yong Zhao ◽  
Hai Yu ◽  
Yanyan Zhang ◽  
...  
Keyword(s):  
Three Dimensional ◽  
Luminescent Properties ◽  
Dimensional Structure ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
Hydrogen Bond Interactions ◽  
Organic Complexes ◽  
Metal Organic ◽  
Complex Features

Two novel ZnII complexes based on a tripodal carboxamide-containing ligand, [Formula: see text] and [Formula: see text] (where LL-2 = N′, N″, N′″-tris(pyrid-2-ylmethyl)-1,3,5-benzenetricarboxamide) are synthesized and structurally characterized. The first complex is a zero-dimensional structure which was further connected into a three-dimensional structure via hydrogen bond interactions, while the second complex features a one-dimensional tube-like structure, where the structural diversities were mainly caused by the different anions. The solid-state luminescent properties of the complexes were investigated and powder X-ray diffraction and thermal gravimetric analysis were performed.

Crystal Structures and Luminescence Behaviour of d10 Metal - Organic Complexes with Multipyridine Ligands

2011 ◽  
Vol 64 (1) ◽  
pp. 104 ◽  
Author(s):  
Chunfeng Yan ◽  
Qihui Chen ◽  
Lian Chen ◽  
Rui Feng ◽  
Xiaochen Shan ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Layer Structure ◽  
Emission Spectra ◽  
Blue Shift ◽  
X Ray Diffraction ◽  
Organic Complexes ◽  
Ligand Charge Transfer ◽  
D10 Metal ◽  
Metal Organic ◽  
Hydrogen Bonded

Six d10 metal–organic complexes with multipyridine ligands, [Cd(terpy)2](NO3)2·2H2O (1), [Cd(terpy)(NO3)2(H2O)] (2), [Hg(terpy)I2] (3), [Zn(tpt)(NO3)(H2O)2]NO3 (4), [Zn2(tpt)2(4,4′-bipy)(4H2O)](NO3)4·4H2O (5), [Zn(tpt)(OAc)2]·5H2O (6) (terpy = 2,2′:6′,2′-terpyridine, tpt = 2,4,6-tri(2-pyridyl)-1,3,5-triazine, 4,4′-bipy = 4,4′-bipyridine) were synthesized and structurally characterized. The abundant hydrogen-bonding interactions extend complex 2 into ladder-like 1D chains, discrete molecules of 4 into a 2D layer structure, complex 5 into a 2D hydrogen-bonded network through linking the hydrogen-bonded ribbons with hexagonal and four-sided rings, and complex 6 into a 3D hydrogen-bonded network through combining water helical chains. Fluorescence analyses of 1–6 in the solid state are investigated at both room temperature and 10 K. The emission spectra of 1–2 show a large red shift, which is ascribed to ligand-to-ligand charge transfer combined with ligand-to-metal charge transfer, whereas emissions of 4–6 all originate from intraligand π-π* transitions. In organic solvents, 1–6 behave very differently and their emission spectra exhibit various luminescences, with an obvious blue shift indicating strong solvent effects. The X-ray diffraction and thermal gravimetric analyses for complexes 1–6 are also reported.

Synthesis, crystal structure, luminescence, and photocatalytic properties of a 2D Cu(II) metal-organic frameworks based on 3,5-di(1H-benzimidazol-1-yl)pyridine and 4,4′-oxybis(benzoate) ligands

2020 ◽  
Vol 75 (8) ◽  
pp. 727-732
Author(s):  
Chen Zhang ◽  
Jian-Qing Tao
Keyword(s):  
Crystal Structure ◽  
Thermal Analysis ◽  
Uv Light ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Light Irradiation ◽  
Photocatalytic Activities ◽  
Metal Organic

AbstractA new Cu(II) metal-organic framework, [Cu(L)(OBA)·H2O]n (1) [H2OBA = 4,4′-oxybis(benzoic acid), L = 3,5-di(1H-benzimidazol-1-yl)pyridine] was hydrothermally synthesized and characterized through IR spectroscopy, elemental and thermal analysis and single-crystal X-ray diffraction. Complex 1 is a four-connected uni-nodal 2D net with a (44·62) topology which shows an emission centered at λ ∼393 nm upon excitation at λ = 245 nm. Moreover, complex 1 possesses high photocatalytic activities for the decomposition of Rhodamine B (RhB) under UV light irradiation.

scholarly journals Four Novel d10 Metal-Organic Frameworks Incorporating Amino-Functionalized Carboxylate Ligands: Synthesis, Structures, and Fluorescence Properties

2021 ◽  
Vol 9 ◽  
Author(s):  
Wang Xie ◽  
Jie Wu ◽  
Xiaochun Hang ◽  
Honghai Zhang ◽  
Kang shen ◽  
...  
Keyword(s):  
Metal Organic Frameworks ◽  
Three Dimensional ◽  
Fluorescence Properties ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Quenching Effect ◽  
D10 Metal ◽  
Metal Organic ◽  
Point Symbol

By employment of amino-functionalized dicarboxylate ligands to react with d10 metal ions, four novel metal-organic frameworks (MOFs) were obtained with the formula of {[Cd(BCPAB)(μ2-H2O)]}n (1), {[Cd(BDAB)]∙2H2O∙DMF}n (2), {[Zn(BDAB)(BPD)0.5(H2O)]∙2H2O}n (3) and {[Zn(BDAB)(DBPB)0.5(H2O)]∙2H2O}n (4) (H2BCPAB = 2,5-bis(p-carbonylphenyl)-1-aminobenzene; H2BDAB = 1,2-diamino-3,6-bis(4-carboxyphenyl)benzene); BPD = (4,4′-bipyridine); DBPB = (E,E-2,5-dimethoxy-1,4-bis-[2-pyridin-vinyl]-benzene; DMF = N,N-dimethylformamide). Complex 1 is a three-dimensional (3D) framework bearing seh-3,5-Pbca nets with point symbol of {4.62}{4.67.82}. Complex 2 exhibits a 4,4-connected new topology that has never been reported before with point symbol of {42.84}. Complex 3 and 4 are quite similar in structure and both have 3D supramolecular frameworks formed by 6-fold and 8-fold interpenetrated 2D coordination layers. The structures of these complexes were characterized by single crystal X-ray diffraction (SC-XRD), thermal gravimetric analysis (TGA) and powder X-ray diffraction (PXRD) measurements. In addition, the fluorescence properties and the sensing capability of 2–4 were investigated as well and the results indicated that complex 2 could function as sensor for Cu2+ and complex 3 could detect Cu2+ and Ag+via quenching effect.

Two Novel One-dimensional Inorganic-Organic Hybrids Constructed from [H2W12O40]6– Clusters and Lanthanide-organic Complexes: [(C5H5N-CO2)2Ln(H2O)3]2[H2W12O40]·nH2O (C5H5N-CO2 = Pyridine-4-carboxylate; Ln = La3+, n = 5; Ce3+, n = 7)

2008 ◽  
Vol 63 (1) ◽  
pp. 16-22 ◽  
Author(s):  
Hai-jun Pang ◽  
Ya-guang Chen ◽  
Fan-xia Meng ◽  
Dong-mei Shi
Keyword(s):  
Lanthanide Complexes ◽  
Rare Earth Compounds ◽  
Bidentate Ligands ◽  
X Ray Diffraction ◽  
Electrolytic Solution ◽  
One Dimensional ◽  
X Ray ◽  
Notable Effect ◽  
Organic Complexes ◽  
Elemental Analyses

Two novel polyoxotungstate-based rare earth compounds, [(C5H5N-CO2)2Ln(H2O)3]2- [H2W12O40] · nH2O (C5H5N-CO2 = pyridine-4-carboxylate; Ln = La3+ (1), n = 5; Ce3+ (2), n = 7), have been synthesized in aqueous solution and characterized by single-crystal X-ray diffraction, elemental analyses, IR spectra and TG analyses. The isostructural compounds 1 and 2 exhibit onedimensional (1D) zig-zag chains, in which the dinuclear lanthanide complexes act as bridging linkers and the [H2W12O40]6− groups serve as bidentate ligands. The results of cyclic voltammetry (CV) show that compounds 1 and 2 undergo two two-electron redox processes, similar to that of the parent (NH4)6[H2W12O40] ·3H2O, and also reveal that the pH of the supporting electrolytic solution has a notable effect on the electrochemical behavior of compound 2.

A new one-dimensional Cd(II) coordination polymer with a two-dimensional supramolecular architecture: synthesis, structural characterization and fluorescence properties

2019 ◽  
Vol 74 (4) ◽  
pp. 341-345
Author(s):  
Kai-Long Zhong ◽  
Wei Song ◽  
Chao Ni ◽  
Guo-Qing Cao
Keyword(s):  
Coordination Polymer ◽  
Fluorescence Properties ◽  
Gravimetric Analysis ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
Organic Structure ◽  
Distorted Octahedral ◽  
Metal Organic ◽  
Crystal Structural

AbstractA new coordination polymer [Cd(C10H8N2)2 (C10H4O8)]n (C10H8N2 = 2,2′-bipyridine and C10H4O8 = 2,5-dicarboxybenzene-1,4-dicarboxylate) has been hydrothermally synthesized and characterized by elemental analysis, infrared spectroscopy, thermal gravimetric analysis and single-crystal X-ray diffraction. Crystal structural analysis reveals that the CdII cation is coordinated by two 2,5-dicarboxybenzene-1,4-dicarboxylate ligands and two 2,2′-bipyridine molecules, forming a distorted octahedral CdN4O2 coordination geometry. The 2,5-dicarboxybenzene-1,4-dicarboxylate ligands link the CdII cations to generate a one-dimensional metal-organic structure running along the [0 1 0] direction. Adjacent chains are further connected by carboxyl-carboxyl O–H···O hydrogen bonds, resulting in a two-dimensional supermolecular architecture running parallel to the (1 0 0) plane in the solid state. The fluorescence properties of the complex were investigated.

scholarly journals A new one-dimensional NiIIcoordination polymer with a two-dimensional supramolecular architecture

2017 ◽  
Vol 73 (2) ◽  
pp. 192-195
Author(s):  
Kai-Long Zhong
Keyword(s):  
Hydrogen Bonds ◽  
Water Molecule ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Sulfate Ions ◽  
Sulfate Anion ◽  
One Dimensional ◽  
X Ray ◽  
Distorted Octahedral ◽  
Metal Organic

A new one-dimensional NiIIcoordination polymer of 1,3,5-tris(imidazol-1-ylmethyl)benzene, namelycatena-poly[[aqua(sulfato-κO)hemi(μ-ethane-1,2-diol-κ2O:O′)[μ3-1,3,5-tris(1H-imidazol-1-ylmethyl)benzene-κ3N3,N3′,N3′′]nickel(II)] ethane-1,2-diol monosolvate monohydrate], {[Ni(SO4)(C18H18N6)(C2H6O2)0.5(H2O)]·C2H6O2·H2O}n, was synthesized and characterized by elemental analysis, IR spectroscopy and single-crystal X-ray diffraction. The NiIIcation is coordinated by three N atoms of three different 1,3,5-tris(imidazol-1-ylmethyl)benzene ligands, one O atom of an ethane-1,2-diol molecule, by a sulfate anion and a water molecule, forming a distorted octahedral NiN3O3coordination geometry. The tripodal 1,3,5-tris(imidazol-1-ylmethyl)benzene ligands link the NiIIcations, generating metal–organic chains running along the [100] direction. Adjacent chains are further connected by O—H...O hydrogen bonds, resulting in a two-dimensional supermolecular architecture running parallel to the (001) plane. Another water molecule and a second ethane-1,2-diol molecule are non-coordinating and are linked to the coordinating sulfate ionsviaO—H...O hydrogen bonds.

Porous Supramolecular Networks Constructed of One-Dimensional Metal–Organic Chains: Carbon Dioxide and Iodine Capture

2015 ◽  
Vol 54 (4) ◽  
pp. 1655-1660 ◽  
Author(s):  
Fei Yu ◽  
Dan-Dan Li ◽  
Lin Cheng ◽  
Zheng Yin ◽  
Ming-Hua Zeng ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
One Dimensional ◽  
Metal Organic ◽  
Supramolecular Networks
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