Search results for "Metal-Organic Framework"

showing 10 items of 194 documents

Metal-Organic Frameworks as Versatile Heterogeneous Solid Catalysts for Henry Reactions

2021

Metal–organic frameworks (MOFs) have become one of the versatile solid materials used for a wide range of applications, such as gas storage, gas separation, proton conductivity, sensors and catalysis. Among these fields, one of the more well-studied areas is the use of MOFs as heterogeneous catalysts for a broad range of organic reactions. In the present review, the employment of MOFs as solid catalysts for the Henry reaction is discussed, and the available literature data from the last decade are grouped. The review is organized with a brief introduction of the importance of Henry reactions and structural properties of MOFs that are suitable for catalysis. The second part of the review dis…

Nitroaldol reactionMaterials sciencePharmaceutical ScienceReviewHeterogeneous catalysisCatalysisAnalytical ChemistryCatalysislcsh:QD241-441metal–organic frameworkslcsh:Organic chemistryCatalytic DomainDrug DiscoveryUreaGas separationAminesPhysical and Theoretical ChemistryMetal-Organic FrameworksHeterogeneous catalysisPrimary (chemistry)Organic ChemistryAmidesOrganic reactionChemical engineeringChemistry (miscellaneous)Molecular MedicineMetal-organic frameworkAmine gas treatingHenry reactionCopperMolecules
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Synthesis of rigid ethynyl-bridged polytopic picolinate ligands for MOF applications

2015

Abstract Segmented homopolytopic ligands that consist of a rigid central arylene platform, ethynylene spacers, and terminal chelating picolinate subunits have been synthesized in good yields in a two-step procedure involving a Sonogashira-type cross coupling reaction between the ester methyl 5-bromopyridine-2-carboxylate and several arylacetylenes, followed by hydrolysis of the resulting methyl picolinates. A similar strategy has been employed for the preparation of heteroditopic ligands containing picolinate and a second non-chelating pyridine or benzoate unit. The compounds are potential candidates for organic linkers in metal–organic frameworks (MOFs).

Organic ChemistryAryleneSonogashira couplingBiochemistryCombinatorial chemistryCoupling reactionchemistry.chemical_compoundHydrolysischemistryDrug DiscoveryPyridineOrganic chemistryMetal-organic frameworkChelationTetrahedron Letters
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Metal-Organic Frameworks as Unique Platforms to Gain Insight of σ-Hole Interactions for the Removal of Organic Dyes from Aquatic Ecosystems.

2022

The combination of high crystallinity and rich host-guest chemistry in metal-organic frameworks (MOFs), have situated them in an advantageous position, with respect to traditional porous materials, to gain insight on specific weak noncovalent supramolecular interactions. In particular, sulfur σ-hole interactions are known to play a key role in the biological activity of living beings as well as on relevant molecular recognitions processes. However, so far, they have been barely explored. Here, we describe both how the combination of the intrinsic features of MOFs, especially the possibility of using single-crystal X-ray crystallography (SCXRD), can be an extremely valuable tool to gain insi…

Organic ChemistryWaterGeneral ChemistryAdsorptionColoring AgentsCatalysisEcosystemMetal-Organic FrameworksSulfurChemistry (Weinheim an der Bergstrasse, Germany)
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Incorporation of metal-organic framework amino-modified MIL-101 into glycidyl methacrylate monoliths for nano LC separation.

2018

Metal-organic frameworks consisting of amino-modified MIL-101(M: Cr, Al, and Fe) crystals have been synthesized and subsequently incorporated to glycidyl methacrylate monoliths to develop novel stationary phases for nano-liquid chromatography. Two incorporation approaches of these materials in monoliths were explored. The metal-organic framework materials were firstly attached to the pore surface through reaction of epoxy groups present in the parent glycidyl methacrylate-based monolith. Alternatively, NH2 -MIL-101(M) were admixed in the polymerization mixture. Using short time UV-initiated polymerization, monolithic beds with homogenously dispersed metal-organic frameworks were obtained. T…

Organic polymergeographyGlycidyl methacrylategeography.geographical_feature_categoryMaterials science010401 analytical chemistryFiltration and Separation02 engineering and technologyEpoxy021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryNano liquid chromatographychemistry.chemical_compoundPolymerizationchemistryChemical engineeringvisual_artvisual_art.visual_art_mediumMetal-organic frameworkMonolith0210 nano-technologyJournal of separation science
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Highly stable and porous porphyrin-based zirconium and hafnium phosphonates – electron crystallography as an important tool for structure elucidation

2018

The Ni-metallated porphyrin-based tetraphosphonic acid (Ni-tetra(4-phosphonophenyl)porphyrin, Ni-H8TPPP) was used for the synthesis of highly porous metal phosphonates containing the tetravalent cations Zr4+ and Hf4+. The compounds were thoroughly characterized regarding their sorption properties towards N2 and H2O as well as thermal and chemical stability. During the synthesis optimization the reaction time could be substantially decreased under stirring from 24 to 3 h in glass vials. M-CAU-30, [M2(Ni-H2TPPP)(OH/F)2]·H2O (M = Zr, Hf) shows exceptionally high specific surface areas for metal phosphonates of aBET = 1070 and 1030 m2 g-1 for Zr- and Hf-CAU-30, respectively, which are very clos…

PORESMaterials scienceChemistry Multidisciplinarychemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesAQUEOUS-SOLUTIONMETAL-ORGANIC FRAMEWORKSchemistry.chemical_compoundDESIGNAUTOMATED DIFFRACTION TOMOGRAPHYFormula unitMoleculeCRYSTAL-STRUCTUREZirconiumScience & TechnologySTABILITYGeneral Chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencesChemistryMANGANESE PORPHYRINSCrystallographychemistryElectron diffractionPhysical SciencesLIGANDSChemical stabilityCyclic voltammetry0210 nano-technologySYSTEMChemical Science
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High-Quality Metal–Organic Framework Ultrathin Films for Electronically Active Interfaces

2016

Currently available methodologies arguably lack the exquisite control required for producing metal-organic framework (MOF) thin films of sufficient quality for electronic applications. By directing MOF transfer with self-assembled monolayers (SAMs), we achieve very smooth, homogeneous, highly oriented, ultrathin films across millimeter-scale areas that display moderate conductivity likely due to electron hopping. Here, the SAM is key for directing the transfer thereby enlarging the number and nature of the substrates of choice. We have exploited this versatility to evolve from deposition onto standard Si and Au to nonconventional substrates such as ferromagnetic Permalloy. We believe that t…

PermalloyChemistryNanotechnology02 engineering and technologyGeneral ChemistryConductivity010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysis0104 chemical sciencesColloid and Surface ChemistryFerromagnetismMonolayerDeposition (phase transition)Metal-organic frameworkElectronicsThin film0210 nano-technologyJournal of the American Chemical Society
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Novel bimetallic MOF phosphors with an imidazolium cation: structure, phonons, high- pressure phase transitions and optical response

2018

We report the synthesis, crystal structure, phonons and luminescence properties of three novel heterometallic metal organic frameworks (MOFs) with perovskite-like topology of the following formulas: [C3H5N2]Na0.5Cr0.5(HCOO)3 (ImNaCr), [C3H5N2]Na0.5Al0.5(HCOO)3 (ImNaAl) and [C3H5N2]Na0.5Al0.475Cr0.025(HCOO)3 (ImNaAlCr with 5 mol% of Cr3+). ImNaCr crystallizes in a monoclinic system (P2/n space group) with one imidazolium cation (Im+) in an asymmetric unit forming six N–H⋯O and four C–H⋯O hydrogen bonds. In contrast to other known heterometallic MOFs, the complete substitution of Cr3+ ions with smaller Al3+ ions leads to a change of the crystal symmetry. ImNaAl adopts a monoclinic P21/n space…

Phase transitionMaterials science010405 organic chemistrySpectrochemical seriesCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCrystalsymbols.namesakeCrystallographysymbolsMetal-organic frameworkRaman spectroscopyLuminescenceMonoclinic crystal systemDalton Transactions
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Confined crystallization of a HKUST-1 metal–organic framework within mesostructured silica with enhanced structural resistance towards water

2017

A HKUST-1 metal–organic framework was crystallized in the NH2-modified mesostructured silica FDU-12 in order to improve its structural stability upon water exposure. In-depth structural characterization studies of the designed composite confirmed successful formation of the MOF phase within the ordered spherical mesopores of the silica matrix. In spite of the confinement within the cavities, MOF exhibits full accessibility for the adsorbed gas molecules. In contrast to the bulk HKUST-1, which undergoes slow phase transition in a humid environment, the structural integrity of the HKUST-1 in the humid-protective matrix remains unchanged even after immersion and stirring in water at elevated t…

Phase transitionMaterials scienceRenewable Energy Sustainability and the EnvironmentComposite numberEngineering controlled terms: Crystalline materialsOrganometallicsStability Compendex keywords Confined crystallizationElevated temperatureMesostructured silicaMetal organic frameworkSpherical mesoporesStructural characterizationStructural resistanceStructural stabilities Engineering main heading: SilicaNanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionAdsorptionChemical engineeringlawPhase (matter)MoleculeGeneral Materials ScienceMetal-organic frameworkCrystallization0210 nano-technologyMesoporous material
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Multitechnique Analysis of the Hydration in Three Different Copper Paddle-Wheel Metal-Organic Frameworks

2019

The structural instability in a humid environment of the majority of metal-organic frameworks (MOFs) is a challenging obstacle for their industrial-scale development. Recently, two water-resistant MOFs have been synthetized, STAM-1 and STAM-17-OEt. They both contain copper paddle wheels, like the well-known water-sensitive HKUST-1, but different organic linkers. The crystal lattice of both the MOFs undergoes a phase transition upon interaction with water molecules. Their unusual flexibility allows the controlled breaking of some interpaddle wheel Cu-O interactions in the so-called crumple zones, with a mechanism called hemilability, which is considered to have a crucial role for the stabili…

Phase transitionMaterials sciencemetal-organic-framework mof electroma paramagnetic resonance epr esr stability hydrationchemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCopper0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionGeneral EnergyPaddle wheelchemistryHemilabilityChemical physicslawMoleculeMetal-organic frameworkPhysical and Theoretical Chemistry0210 nano-technologyElectron paramagnetic resonance
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Mechanism of water adsorption in the large pore form of the gallium-based MIL-53 metal-organic framework

2016

Abstract Water adsorption in the large pore ( lp_empty ) form of Ga-MIL-53 was studied by TGA, DSC and in situ XRD and FTIR at 298 K. The large pore form can be stabilized at room temperature after activation under vacuum at 553 K. The isotherm of water adsorption in this large pore form (pore dimensions: 1.67 × 1.33 nm) is very similar to that measured on the narrow pore ( np_empty ) form (pore dimensions: 1.97 × 0.76 nm). Such a similarity is rather unusual given that the pore sizes of these two phases are very different. In order to understand the origin of this effect in situ XRD and FTIR measurements were particularly helpful. It was found that the adsorption of even small amount of wa…

Phase transitionchemistry.chemical_elementMineralogy02 engineering and technology010402 general chemistry01 natural sciencesAdsorptionPhase (matter)AtomMolecule[CHIM]Chemical SciencesGeneral Materials ScienceGalliumFourier transform infrared spectroscopyComputingMilieux_MISCELLANEOUSGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryChemical engineeringMechanics of MaterialsMetal-organic framework0210 nano-technology
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