Search results for "Metal-organic framework"

showing 10 items of 194 documents

Trimesic acid on Cu in ethanol: Potential-dependent transition from 2-D adsorbate to 3-D metal-organic framework

2017

We report the potential-dependent interactions of trimesic acid with Cu surfaces in EtOH. CV experiments and electrochemical surface-enhanced Raman spectroscopy show the presence of an adsorbed trimesic acid layer on Cu at potentials lower than 0 V vs Cu. The BTC coverage increases as the potential increases, reaching a maximum at 0 V. Based on molecular dynamics simulations, we report adsorption geometries and possible structures of the organic adlayer. We find that, depending on the crystal facet, trimesic acid adsorbs either flat or with one or two of the carboxyl groups facing the metal surface. At higher coverages, a multi-layer forms that is composed mostly of flat-lying trimesic acid…

General Chemical EngineeringInorganic chemistrySelf-assembled monolayers02 engineering and technology010402 general chemistryElectrochemistry01 natural sciencesAnalytical ChemistryMetalMolecular dynamicschemistry.chemical_compoundAdsorptionOrganic electrolytesElectrochemistryMoleculeQuímica FísicaChemistryCu UPDSelf-assembled monolayerMetal-organic frameworks021001 nanoscience & nanotechnology0104 chemical sciencesvisual_artvisual_art.visual_art_mediumMetal-organic frameworkTrimesic acid0210 nano-technologyJournal of Electroanalytical Chemistry
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Expanding the Variety of Zirconium‐based Inorganic Building Units for Metal–Organic Frameworks

2019

Two new zirconium-based metal-organic frameworks with the composition [Zr6 O4 (OH)4 (OAc)6 (BDC)3 ] (CAU-26) and [Zr5 O4 (OH)4 (OAc)4 (BDC)2 ] (CAU-27) are reported, which were synthesized from acetic acid, a rarely utilized but green and sustainable solvent (BDC2- : 1,4-benzenedicarboxylate). Structure determination aided by automated electron diffraction tomography revealed that CAU-26 is composed of layers of well-known {Zr6 O8 } clusters interconnected by terephthalate ions. In contrast CAU-27 exhibits a three-dimensional structure with a so far unknown type of one-dimensional inorganic building unit (IBU), which can be rationalized as condensed polyhedron-sharing chains of {Zr6 O8 } cl…

Green chemistryMaterials scienceChemistry MultidisciplinaryCATALYZED BORYLATIONchemistry.chemical_element010402 general chemistryHIGHLY EFFICIENTBorylation01 natural sciencesTOXICITYCatalysisCatalysisAUTOMATED DIFFRACTION TOMOGRAPHYPolymer chemistryMoleculeZR-MOFGreen ChemistryZirconiumScience & TechnologySTABILITY010405 organic chemistryDirect C-H borylationGeneral ChemistryGeneral MedicineElectron DiffractionORGANOSILICA0104 chemical sciencesSolventChemistrychemistryPhysical SciencesARENESMetal-organic frameworkChemical stabilityZirconiumCLUSTERSMetal-organic FrameworksGREEN SYNTHESISAngewandte Chemie
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The oxamate route, a versatile post-functionalization for metal incorporation in MIL-101(Cr): Catalytic applications of Cu, Pd, and Au

2013

Abstract A new consecutive post-functionalization method has been developed for the inclusion of additional metal functionalities in Metal Organic Frameworks (MOFs) through oxamate as chelating agent. This may result in catalytic centers of metal–organic complexes or in controlled formation of metal nanoparticles, demonstrated for Cu, Pd and Au, in the highly stable MIL-101(Cr) framework. In a first post-synthesis step, reduction of the NO 2 -MIL-101(Cr) leads to the formation of NH 2 -MIL-101(Cr). The second functionalization consists of a straightforward condensation of the amino groups of the ligand with ethyl chloro-oxoacetate resulting in the formation of free oxamates attached to the …

Heterogeneous catalysisChemistryInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisCopperPost-functionalizationCatalysisCoupling reactionCatalysisMetalMetal complexMetal organic frameworkColloidal goldNH2-MIL-101(Cr)visual_artvisual_art.visual_art_mediumNanoparticlesMetal-organic frameworkOxamateGoldPhysical and Theoretical ChemistryPalladiumCopperPalladium
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Stabilized Ru[(H2O)(6)](3+) in Confined Spaces (MOFs and Zeolites) Catalyzes the lmination of Primary Alcohols under Atmospheric Conditions with Wide…

2018

[EN] Imines are ubiquitous intermediates in organic synthesis, and the metal-mediated imination of alcohols is one of the most direct and simple methods for their synthesis. However, reported protocols lack compatibility with many other functional groups since basic supports/media, pure oxygen atmospheres, and/or released hydrogen gas are required during reaction. Here we show that, in contrast to previous metal-catalyzed methods, hexa-aqueous Ru(III) catalyzes the imination of primary alcohols with very wide functional group tolerance, at slightly acid pH and under low oxygen atmospheres. The inorganic metal complex can be supported and stabilized, integrally, within either faujasite-type …

HydrogenMetal-organic frameworkIminechemistry.chemical_element02 engineering and technology010402 general chemistryHeterogeneous catalysis01 natural sciencesRutheniumCatalysisCatalysischemistry.chemical_compoundQUIMICA ORGANICAImineZeoliteZeoliteGeneral Chemistry021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesRutheniumchemistryMetal-organic frameworkOrganic synthesis0210 nano-technology
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Spin‐Crossover 2D Metal–Organic Frameworks with a Redox‐Active Ligand: [Fe(ttf‐adpy) 2 M(CN) 4 ]· n H 2 O (ttf‐adpy = 4‐Tetrathiafulvalenylcarboxamid…

2008

A new ttf (tetrathiofulvalene) ligand containing an amidopyridine moiety was synthesized and characterized. The electrochemical study of the 4-tetrathiofulvalenylcarboxamidopyridine (ttf–adpy) ligand showed two reversible oxidation processes at EI′1/2 = 0.08 V/Fc+–Fc and EII′1/2 = 0.26 V/Fc+–Fc. The crystal structure of [(ttf–adpyH)2Pt(CN)4] (1) was solved at 293 K, where 1 displays the triclinic space group P. The ttf–adpyH+ molecule is planar, and the bond lengths within the ttf core are in the usual range for neutral ttf moieties. The ttf–adpyH+ molecules and the [Pt(CN)4]2– anions organize in a three-dimensional network by means of hydrogen bonds and short S···S contacts. In the network…

Inorganic ChemistryCrystallographyChemistryHydrogen bondLigandSpin crossoverInorganic chemistrySpin transitionMoleculeMetal-organic frameworkCrystal structureAcceptorEuropean Journal of Inorganic Chemistry
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Mixed component metal-organic frameworks: Heterogeneity andcomplexity at the service of application performances

2022

The synthesis of mixed-component metal-organic frameworks (MOFs) –including multivariate MOFs (MTV-MOFs), multicomponent MOFs, mixed-metals MOFs and mixed-ligands and metals MOFs– is becoming a very active research field. This is mainly based on the unique possibilities these materials offer to incorporate multiple functionalities and in how this heterogenity and complexity is translated in unexpected properties, which are not just the sum of each component. This review critically encompasses the progress made in this field, covering the synthetic approaches, and specially focusing on the current reported applications –such as gas storage and separation, catalysis, luminescence, conductivit…

Inorganic ChemistryService (systems architecture)010405 organic chemistryChemistryComponent (UML)Materials ChemistryNanotechnologyMetal-organic frameworkPhysical and Theoretical Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesCoordination Chemistry Reviews
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Highly Efficient Removal of Neonicotinoid Insecticides by Thioether-Based (Multivariate) Metal–Organic Frameworks

2021

Circumventing the impact of agrochemicals on aquatic environments has become a necessity for health and ecological reasons. Herein, we report the use of a family of five eco-friendly water-stable isoreticular metal-organic frameworks (MOFs), prepared from amino acids, as adsorbents for the removal of neonicotinoid insecticides (thiamethoxam, clothianidin, imidacloprid, acetamiprid, and thiacloprid) from water. Among them, the three MOFs containing thioether-based residues show remarkable removal efficiency. In particular, the novel multivariate MOF {SrIICuII6[(S,S)-methox]1.5[(S,S)-Mecysmox]1.50(OH)2(H2O)}·36H2O (5), featuring narrow functional channels decorated with both -CH2SCH3 and -CH2…

InsecticidesMaterials science02 engineering and technologySulfides010402 general chemistry01 natural sciencesAcetamipridWater PurificationNeonicotinoidschemistry.chemical_compoundMethionineAdsorptionThioetherOrganic chemistryGeneral Materials ScienceCysteineMetal-Organic FrameworksSolid Phase ExtractionNeonicotinoidClothianidin021001 nanoscience & nanotechnologyThiacloprid0104 chemical scienceschemistryMetal-organic frameworkAdsorptionThiamethoxam0210 nano-technologyWater Pollutants Chemicalacs applied materials & interfaces
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Metal–Organic Frameworks as Playgrounds for Reticulate Single-Molecule Magnets

2019

Achieving an accurate control on the final structure of Metal-Organic Frameworks (MOFs) is mandatory to obtain target physical properties. Here we describe how the combination of a metalloligand design strategy and a post-synthetic method is a versatile and powerful approach to success on this extremely difficult task. In a first stage, a novel oxamato-based tetranuclear cobalt(III) complex with a tetrahedron-shape geometry is used, for the first time, as metalloligand toward cal-cium(II) cations to lead a diamagnetic Ca(II)-Co(III) three-dimensional (3D) MOF (1). In a second stage, in a single-crystal to single-crystal manner the calcium(II) ions are replaced by terbium (III), dysprosium(I…

Lanthanide010405 organic chemistryMetal ions in aqueous solutionQuímica organometàl·licachemistry.chemical_elementTerbium010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryCrystallographychemistryDysprosiumMoleculeMetal-organic frameworkPhysical and Theoretical ChemistryIsostructuralInorganic Chemistry
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The construction of open GdIII metal–organic frameworks based on methanetriacetic acid: New objects with an old ligand

2010

11 páginas, 11 figuras, 2 esquemas.-- et al.

LanthanideGadoliniumchemistry.chemical_elementGadoliniumAcetatesCrystallography X-RayLigandsLanthanoid Series ElementsTopologyCatalysisMagnetic propertiesOrganometallic CompoundsMolecular StructureMetal–organic frameworksLigandOrganic ChemistryGeneral ChemistryTrigonal prismatic molecular geometryX-ray diffractionCrystallographychemistryOctahedronTripodal ligandX-ray crystallographyMetal-organic framework
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Divergent Adsorption-Dependent Luminescence of Amino-Functionalized Lanthanide Metal-Organic Frameworks for Highly Sensitive NO2 Sensors

2020

International audience; A novel gas sensing mechanism exploiting lanthanide luminescence modulation upon NO2 adsorption is demonstrated here. Two isostructural lanthanide-based metal–organic frameworks (MOFs) are used, including an amino group as the sensitive recognition center for NO2 molecules. The transfer of energy from the organic ligands to Ln is strongly dependent on the presence of NO2, resulting in an unprecedented photoluminescent sensing scheme. Thereby, NO2 exposition triggers either a reversible enhancement or a decrease in the luminescence intensity, depending on the lanthanide ion (Eu or Tb). Our experimental studies combined with density functional theory and complete activ…

LanthanideIonsPhotoluminescenceLuminescenceChemistryLigandAb initioMetal organic frameworks02 engineering and technology[CHIM.MATE]Chemical Sciences/Material chemistryMolecules010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryLigands01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryAdsorptionGeneral Materials ScienceMetal-organic frameworkPhysical and Theoretical ChemistryIsostructural0210 nano-technologyLuminescence
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