scholarly journals Magnetism and Luminescence of a MOF with Linear Mn3 Nodes Derived from an Emissive Terthiophene-Based Imidazole Linker

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4286
Author(s):  
Weiran Wang ◽  
Junpeng He ◽  
Hongyu Guo ◽  
Samuel G. Dunning ◽  
Simon M. Humphrey ◽  
...  
Keyword(s):  
Photophysical Properties ◽  
Metal Organic Framework ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
Secondary Building Unit ◽  
X Ray ◽  
Dual Functional ◽  
Metal Organic ◽  
One Step ◽  
Solvothermal Conditions

A new terthiophene-based imidazole luminophore 5,5’-(1H-thieno[3,4-d]imidazole-4,6-diyl)bis(thiophene-2-carboxylic acid) (TIBTCH2, 5) was synthesized in one step from previously reported 4,6-di(thiophen-2-yl)-1H-thieno[3,4-d]imidazole (DTTI, 4), and their photophysical properties were studied and compared accordingly. Under solvothermal conditions, reacting 5 with Mn(OAc)2 yielded a new three-dimensional metal-organic framework (MOF, 6) which was structurally defined by single-crystal X-ray diffraction. In 6, all Mn(II) ions octahedrally bind to carboxylate-O atoms to form a linear Mn3 secondary building unit (SBU) that contains three distinct coordination modes. Importantly, 6 exhibits dual functional properties of ligand-based emission and metal-based magnetic behaviors.

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.

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.

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

scholarly journals Synthesis of a Novel Porphyrin-Based Metal–Organic Framework (Co-Por MOF)

Proceedings ◽  
2019 ◽  
Vol 41 (1) ◽  
pp. 83
Author(s):  
Leyla Tayebi ◽  
Rahmatollah Rahimi ◽  
Mahboubeh Rabbani
Keyword(s):  
Solvothermal Method ◽  
Metal Organic Framework ◽  
Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Covalent Interaction ◽  
Metal Organic ◽  
One Step ◽  
Organic Linker ◽  
Organic Framework

In this study, a novel porphyrin-based metal–organic framework (Co-Por MOF) was successfully synthesized by a simple one-step solvothermal method. We report a metal–organic framework based on the covalent interaction of an organic linker, 5,10,15,20-tetrakis(4-carboxyphenyl) porphyrin (TCPP) with cobalt clusters. The properties of this material were analyzed by powder X-ray diffraction (XRD), ultraviolet visible adsorption spectroscopy (UV–Vis), Fourier-transform infrared spectroscopy (FTIR), and differential reflectance spectroscopy (DRS).

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.

A multifunctional colorimetric sensors originated from a cadmium naphthalene diimide-based metal-organic framework: photochromism, hydrochromism, and vapochromism

CrystEngComm ◽  
2021 ◽  
Author(s):  
Guoshuai Zhang ◽  
Chen Fu ◽  
Heyi Zhang ◽  
Hong Zhang
Keyword(s):  
Ir Spectroscopy ◽  
Metal Organic Framework ◽  
X Ray Diffraction ◽  
X Ray ◽  
Naphthalene Diimide ◽  
Elemental Analyses ◽  
Cadmium Metal ◽  
Metal Organic ◽  
Solvothermal Conditions ◽  
Organic Framework

A new cadmium metal-organic framework [Cd(IsoNDI)(ClO4)·H2O]n (ZH-102, IsoNDI = N,N′-di(4-pyridylacylamino)-1,4,5,8-naphthalene diimide) has been synthesized under solvothermal conditions and characterized systematically by elemental analyses, IR spectroscopy, powder X-ray diffraction, and thermogravimetric...

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