Synthesis, structure and photocatalytic degradation of organic dyes of a copper(II) metal–organic framework (Cu–MOF) with a 4-coordinated three-dimensional CdSO4 topology

2019 ◽  
Vol 75 (8) ◽  
pp. 1053-1059 ◽  
Author(s):  
Lin-Lu Qian ◽  
Zhi-Xiang Wang ◽  
Hai-Xin Tian ◽  
Min Li ◽  
Bao-Long Li ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Crystal Engineering ◽  
Photoelectron Spectroscopy ◽  
Organic Dyes ◽  
Metal Organic Framework ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metal Organic ◽  
And Storage

Metal–organic frameworks (MOFs) have attracted much interest in the fields of gas separation and storage, catalysis synthesis, nonlinear optics, sensors, luminescence, magnetism, photocatalysis gradation and crystal engineering because of their diverse properties and intriguing topologies. A Cu–MOF, namely poly[[(μ2-succinato-κ2 O:O′){μ2-tris[4-(1,2,4-triazol-1-yl)phenyl]amine-κ2 N:N′}copper(II)] dihydrate], {[Cu(C4H4O4)(C24H18N10)]·2H2O} n or {[Cu(suc)(ttpa)]·2H2O} n , (I), was synthesized by the hydrothermal method using tris[4-(1,2,4-triazol-1-yl)phenyl]amine (ttpa) and succinate (suc2−), and characterized by IR, powder X-ray diffraction (PXRD), luminescence, optical band gap and valence band X-ray photoelectron spectroscopy (VB XPS). Cu–MOF (I) shows a twofold interpenetrating 4-coordinated three-dimensional CdSO4 topology with point symbol {65·8}. It presents good photocatalytic degradation of methylene blue (MB) and rhodamine B (RhB) under visible-light irradiation. A photocatalytic mechanism was proposed and confirmed.

Ferromagnetic interactions in a dicyanamide-bridged multinuclear metal-organic framework [Pr3NH]+ [Mn(dca)3]−·H2O

2019 ◽  
Vol 74 (6) ◽  
pp. 485-489
Author(s):  
Yuan Huang ◽  
Xiu-feng Yu ◽  
Zhen Rong ◽  
Yi-chun Ai ◽  
Kun Qian ◽  
...  
Keyword(s):  
Magnetic Susceptibility ◽  
Magnetic Measurements ◽  
Metal Organic Framework ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Magnetic Susceptibility Data ◽  
X Ray ◽  
Susceptibility Data ◽  
Metal Organic ◽  
Ferromagnetic Interactions

AbstractA new complex [Pr3NH]+ [Mn(dca)3]− · H2O (dicyanamide = dca−) was synthesized, in which the Mn2+ cations are bridged by end-to-end dca anions to form three-dimensional [Mn(dca)3]nn− networks and tripropylammonium cations reside in the cavities of these networks. The complex has been characterized by single-crystal X-ray diffraction, infrared spectroscopy, elemental analysis, and magnetic measurements. Magnetic susceptibility data indicate ferromagnetic interactions among the MnII ions.

scholarly journals Metal-Organic Framework MIL-101: Synthesis and Photocatalytic Degradation of Remazol Black B Dye

2019 ◽  
Vol 2019 ◽  
pp. 1-15 ◽  
Author(s):  
Pham Dinh Du ◽  
Huynh Thi Minh Thanh ◽  
Thuy Chau To ◽  
Ho Sy Thang ◽  
Mai Xuan Tinh ◽  
...  
Keyword(s):  
Photocatalytic Degradation ◽  
Photoelectron Spectroscopy ◽  
Metal Organic Framework ◽  
Nitrogen Adsorption ◽  
X Ray ◽  
Remazol Black B ◽  
Metal Organic ◽  
Degradation Reaction ◽  
Remazol Black ◽  
Organic Framework

In the present paper, the synthesis of metal-organic framework MIL-101 and its application in the photocatalytic degradation of Remazol Black B (RBB) dye have been demonstrated. The obtained samples were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption/desorption isotherms at 77 K. It was found that MIL-101 synthesized under optimal conditions exhibited high crystallinity and specific surface area (3360 m2·g-1). The obtained MIL-101 possessed high stability in water for 14 days and several solvents (benzene, ethanol, and water at boiling temperature). Its catalytic activities were evaluated by measuring the degradation of RBB in an aqueous solution under UV radiation. The findings show that MIL-101 was a heterogeneous photocatalyst in the degradation reaction of RBB. The mechanism of photocatalysis was considered to be achieved by the electron transfer from photoexcited organic ligands to metallic clusters in MIL-101. The kinetics of photocatalytic degradation reaction were analyzed by using the initial rate method and Langmuir-Hinshelwood model. The MIL-101 photocatalyst exhibited excellent catalytic recyclability and stability and can be a potential catalyst for the treatment of organic pollutants in aqueous solutions.

scholarly journals Quinone-modified metal-organic frameworks MIL-101(Fe) as heterogeneous catalysts of persulfate activation for degradation of aqueous organic pollutants

2019 ◽  
Vol 79 (12) ◽  
pp. 2357-2365 ◽  
Author(s):  
Huaisu Guo ◽  
Weilin Guo ◽  
Yang Liu ◽  
Xiaohua Ren
Keyword(s):  
Photoelectron Spectroscopy ◽  
Heterogeneous Catalysts ◽  
Electrochemical Impedance ◽  
Metal Organic Framework ◽  
Optimum Conditions ◽  
X Ray Diffraction ◽  
Heterogeneous Fenton ◽  
X Ray ◽  
Metal Organic ◽  
Persulfate Activation

Abstract In this work, quinone-modified metal-organic framework MIL-101(Fe)(Q-MIL-101(Fe)), as a novel heterogeneous Fenton-like catalyst, was synthesized for the activation of persulfate (PS) to remove bisphenol A (BPA). The synthetic Q-MIL-101(Fe) was characterized via X-ray diffraction, scanning electron microscope, Fourier transform infrared, electrochemical impedance spectroscopy, cyclic voltammetry and X-ray photoelectron spectroscopy. As compared to the pure MIL-101(Fe), Q-MIL-101(Fe) displayed better catalytic activity and reusability. The results manifested that the Q-MIL-101(Fe) kept quinone units, which successfully promoted the redox cycling of Fe3+/Fe2+ and enhanced the removal efficiency. In addition, the reaction factors of Q-MIL-101(Fe) were studied (e.g. pH, catalyst dosage, PS concentration and temperature), showing that the optimum conditions were [catalyst] = 0.2 g/L, [BPA] = 60 mg/L, [PS] = 4 mmol/L, pH = 6.79, temperature = 25 °C. On the basis of these findings, the probable mechanism on the heterogeneous activation of PS by Q-MIL-101(Fe) was proposed.

A new three-dimensional twofold interpenetrated cadmium(II) metal–organic framework: synthesis, structure and photoluminescence properties

2021 ◽  
Vol 77 (11) ◽  
Author(s):  
Hong-Tao Zhang ◽  
Xiao-Long Wang
Keyword(s):  
Metal Organic Framework ◽  
Three Dimensional ◽  
Fluorescence Emission ◽  
Functional Materials ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Design And Synthesis ◽  
Metal Organic ◽  
Organic Framework

The design and synthesis of metal–organic frameworks (MOFs) have attracted much interest due to the aesthetics of their crystalline architectures and their potential applications as new functional materials. A new twofold interpenetrated three-dimensional (3D) MOF, namely, poly[[triaqua(μ4-(2R,2′R)-2,2′-{[1,4-phenylenebis(carbonyl)]bis(azanediyl)}dipropionato-κ7 O 1:O 1,O 1′:O 4:O 4,O 4′,O 4′′)(μ3-(2R,2′R)-2,2′-{[1,4-phenylenebis(carbonyl)]bis(azanediyl)}dipropionato-κ3 O 1:O 4:O 4)dicadmium(II)] dihydrate], {[Cd2(C14H14N2O6)2(H2O)3]·2H2O} n , (I), has been synthesized by the reaction of Cd(CH3COO)2·2H2O with the synthesized ligand (2R,2′R)-2,2′-{[1,4-phenylenebis(carbonyl)]bis(azanediyl)}dipropionic acid (H2 L). Single-crystal X-ray diffraction analysis reveals that the carboxylate groups from two crystallographically independent L 2− dianions link the cadmium cations into a one-dimensional helical secondary building unit (SBU). The resulting SBUs are extended into a 3D metal–organic framework via the terephthalamide moiety of the ligand as a spacer. In the crystal, two independent MOFs interpenetrate each other, thus producing a twofold interpenetrated 3D architecture, which shows an unprecedented 2-nodal (7,9)-connected net with the point (Schläfli) symbol (37·46·58)(38·411·516·6). MOF (I) was further characterized by elemental analysis, IR spectroscopy, powder X-ray diffraction and thermogravimetric analysis. The photoluminescence properties and UV–Vis absorption spectrum of (I) have also been investigated. The MOF exhibits enhanced fluorescence emission with a high photoluminescence quantum yield of 31.55% and a longer lifetime compared with free H2 L.

A fivefold interpenetrating diamondoid three-dimensional metal–organic framework constructed from benzene-1,4-diacetic acid and flexible triazole derivatives: poly[[(μ2-benzene-1,4-diacetato-κ2O:O){μ2-1,4-bis[(1H-1,2,4-triazol-1-yl)methyl]benzene-κ2N4:N4′}zinc(II)] monohydrate]

2013 ◽  
Vol 70 (1) ◽  
pp. 28-30 ◽  
Author(s):  
Hong Shen
Keyword(s):  
Metal Organic Framework ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Polymeric Compound ◽  
X Ray ◽  
Twofold Axis ◽  
Carboxylate Groups ◽  
Metal Organic ◽  
Methyl Benzene ◽  
Organic Framework

In the title mixed-ligand metal–organic polymeric compound, {[Zn(C10H8O4)(C12H14N6)]·H2O}n, the asymmetric unit contains a divalent ZnIIcation lying on a twofold axis, one half of a fully deprotonated benzene-1,4-diacetate (PBEA) ligand, one half of a 1,4-bis[(1H-1,2,4-triazol-1-yl)methyl]benzene (BTX) ligand and a water molecule, also lying on a twofold axis. Each ZnIIcentre is surrounded by two O-donor atoms from monodentate carboxylate groups belonging to two different PBEA2−ligands and by two triazole N-donor atoms from two different BTX ligands. Single-crystal X-ray diffraction analysis revealed that the compound has a fivefold interpenetrating diamondoid three-dimensional metal–organic framework.

scholarly journals New Topologically Unique Metal-Organic Architectures Driven by a Pyridine-Tricarboxylate Building Block

Crystals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 353 ◽  
Author(s):  
Jinzhong Gu ◽  
Yan Cai ◽  
Min Wen ◽  
Zhijun Ge ◽  
Alexander Kirillov
Keyword(s):  
Building Block ◽  
Terephthalic Acid ◽  
Metal Organic Framework ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Topological Features ◽  
Metal Organic ◽  
Opening Up ◽  
Luminescent Behavior

Two new three-dimensional (3D) coordination compounds, namely a lead(II) coordination polymer (CP) {[Pb3(µ5-cpta)(µ6-cpta)(phen)2]·2H2O}n (1) and a zinc(II) metal-organic framework (MOF) {[Zn2(µ4-cpta)(µ-OH)(µ-4,4′-bipy)]·6H2O}n (2), were hydrothermally assembled from 2-(5-carboxypyridin-2-yl)terephthalic acid (H3cpta) as an unexplored principal building block and aromatic N,N-donors as crystallization mediators. Both products were isolated as air-stable microcrystalline solids and were fully characterized by IR spectroscopy, elemental and thermogravimetric analysis, and powder and single-crystal X-ray diffraction. Structural and topological features of CP 1 and MOF 2 were analyzed in detail, allowing to identify a topologically unique 4,5,5,6-connected net in 1 or a very rare 4,4-connected net with the isx topology in 2. Thermal stability and solid-state luminescent behavior of 1 and 2 were also investigated. Apart from revealing a notable topological novelty, both compounds also represent the first structurally characterized Pb(II) and Zn(II) derivatives assembled from H3cpta, thus opening up the application of this unexplored pyridine-tricarboxylate block in the design of new metal-organic architectures.

Assembly of 1,2,3,4-Benzenetetracarboxylic Acid and Zinc(II) Metal Centers to a Chiral 3D Metal-organic Framework: Syntheses, Structure and Properties

2011 ◽  
Vol 66 (5) ◽  
pp. 533-537
Author(s):  
Can Ji ◽  
Shuang-Quan Zang ◽  
Jun-Yi Liu ◽  
Jia-Bin Li ◽  
Hong-Wei Hou
Keyword(s):  
Second Harmonic ◽  
Bulk Material ◽  
Metal Organic Framework ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Metal Centers ◽  
X Ray ◽  
Metal Organic ◽  
The Individual ◽  
Organic Framework

A new three-dimensional metal-organic framework {[Zn(mpda)0.5(bix)]·(H2O)1.5}n (1) (H4mpda = 1,2,3,4-benzenetetracarboxylic acid, m-bix = 1,3-bis(imidazol-1-ylmethyl)-benzene) has been synthesized and characterized by single-crystal X-ray diffraction and IR spectra. In 1, homochiral helical chains are formed in the Zn-mpda layer through spontaneous resolution by mpda4−. Such layers are further connected through the second m-bix ligand to form a 3D chiral metal-organic framework. The individual (4,4)-connected net in 1 can be specified by the Schläfli symbol (66)2(64.82). Bulk material of 1 has good second-harmonic generation (SHG) activity, approximately 0.4 times that of urea. In addition, a thermogravimetric analysis was carried out, and the photoluminescent behavior of the complex was also investigated

Enhanced Microwave Absorption Properties of Metal Organic Framework (MOF)-Derived Carbonaceous ZnO Incorporated Reduced Graphene Oxide Composites

NANO ◽  
2019 ◽  
Vol 14 (01) ◽  
pp. 1950005 ◽  
Author(s):  
Zhongfei Liu ◽  
Jiangtao Yuan ◽  
Hui Zhang ◽  
Kuangwei Xiong ◽  
Shaowei Jin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Metal Organic Framework ◽  
X Ray Diffraction ◽  
Microwave Absorption Properties ◽  
X Ray ◽  
Transmission Electron ◽  
Reduced Graphene ◽  
Metal Organic ◽  
Oxide Composites

In this paper, the MOFs-derived carbonaceous ZnO and RGO (carbonaceous ZnO/RGO) composites have been prepared by the wet chemical method and carbonization process. The as-prepared products are characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy (TEM), Raman spectra, thermogravimetric (TG) analysis and X-ray photoelectron spectroscopy (XPS). The electromagnetic parameters of carbonaceous ZnO/RGO composites are investigated by the vector network analyzer. The results exhibit carbonaceous ZnO/RGO composites have a maximum absorption of [Formula: see text][Formula: see text]dB at 6[Formula: see text]GHz with thickness of 3.5[Formula: see text]mm and the effective absorption (below [Formula: see text][Formula: see text]dB) bandwidth is up to 1.92[Formula: see text]GHz (from 5.28 to 7.2[Formula: see text]GHz). Thus, the carbonaceous ZnO/RGO composites have great potential in the field of electromagnetic wave absorption.

Construction of CuII Cluster-Based Magnetic Metal–Organic Framework Derived from a V-Shaped Aromatic Dicarboxylate Ligand

2015 ◽  
Vol 68 (3) ◽  
pp. 416 ◽  
Author(s):  
Yong-Qiang Chen ◽  
Yuan Tian ◽  
Jun Li
Keyword(s):  
Rational Design ◽  
Metal Organic Framework ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Magnetic Metal ◽  
Metal Organic ◽  
Coordination Framework ◽  
Systematic Synthesis

In our efforts towards rational design and systematic synthesis of cluster-based metal–organic frameworks, a new CuII coordination framework derived from the V-shaped aromatic dicarboxylate with formula [Cu4(µ4-O)(L)3]∞ (1), H2L = (4-phenyl)-2,6-bis(4-carboxyphenyl)pyridine) was synthesised under hydrothermal conditions and structurally characterised by single-crystal X-ray diffraction, powder X-ray diffraction, elemental analysis, and infrared spectroscopy. Structure analysis shows that complex 1 has a three-dimensional framework based on [Cu8] cluster with 8-connected bcu topology. Magnetic investigation suggests that anti-ferromagnetic coupling exists between CuII ions in the [Cu8] cluster.

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