Search results for "Metal-organic Frameworks"

showing 10 items of 68 documents

Hybrid Inorganic‐Organic White Light Emitting Diodes

2020

This chapter reviews the state of the art of materials, technologies, characterizations, process and challenges concerning hybrid white light‐emitting diodes (LEDs). Here, for a “hybrid LED” we mean a device based on a layer of organic phosphors (or a mix of inorganic and organic ones) pumped by a high‐energy inorganic LED. Light is emitted by a frequency down‐conversion (sometimes simply named color‐conversion) process. Benefits and weak spots of this technology are investigated with a special attention for the materials involved into the process of frequency down‐conversion, in order to envisage the future impact of the hybrid lighting technology among the well‐established inorganic ones.

Materials sciencebusiness.industryWhite lightOptoelectronicsMetal-organic frameworkInorganic organicbusinessHybrid Inorganic-Organic White Light Emitting Diodes (HWLEDs) Frequency-down conversion Luminescent polymers and molecular dyes Biomaterials and biomolecules Metal-Organic Frameworks Carbon dots Color tuning and rendering of HWLEDs Stability of HWLEDsSettore ING-INF/01 - ElettronicaDiode
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Tetrazine Linkers as Plug-and-Play Tags for General Framework Functionalization and C60 Conjugation

2022

The value of covalent post-synthetic modification in expanding the chemistry and pore versatility of reticular solids is well documented. Here we use mesoporous crystals of UiO-68-TZDC to demonstrate the value of tetrazine connectors for all-purpose inverse electron-demand Diels-Alder ligation chemistry. Our results suggest a positive effect of tetrazine reticulation over its reactivity for quantitative one-step functionalization with a broad scope of alkene or alkyne dienophiles into pyridazine and dihydropyridazine frameworks. This permits generating multiple pore environments with diverse chemical functionalities and the expected accessible porosities, that is also extended to the synthe…

Metal-Organic Frameworks • tetrazine tags • Click chemistry • Diels-Alder • Fullerene
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Chemical Engineering of Photoactivity in Heterometallic Titanium–Organic Frameworks by Metal Doping

2018

[EN] We report a new family of titanium-organic frameworks that enlarges the limited number of crystalline, porous materials available for this metal. They are chemically robust and can be prepared as single crystals at multi-gram scale from multiple precursors. Their heterometallic structure enables engineering of their photoactivity by metal doping rather than by linker functionalization. Compared to other methodologies based on the post-synthetic metallation of MOFs, our approach is well-fitted for controlling the positioning of dopants at an atomic level to gain more precise control over the band-gap and electronic properties of the porous solid. Changes in the band-gap are also rationa…

Metal-organic frameworks PhotocatalysisMaterials scienceQuímica organometàl·licachemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisMetalQUIMICA ORGANICATitaniumDopant010405 organic chemistryDopingGeneral MedicineTitaniGeneral Chemistry0104 chemical sciencesMetal dopingChemical engineeringchemistryvisual_artvisual_art.visual_art_mediumPhotocatalysisSurface modificationBand-gap engineeringMetal-organic frameworkPorous mediumTitaniumAngewandte Chemie International Edition
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Bioinspired Metal-Organic Frameworks in Mixed Matrix Membranes for Efficient Static/Dynamic Removal of Mercury from Water

2020

The mercury removal efficiency of a novel metal-organic framework (MOF) derived from the amino acid S-methyl-L-cysteine is presented and the process is characterized by single-crystal X-ray crystallography. A feasibility study is further presented on the performance of this MOF and also that of another MOF derived from the amino acid L-methionine when used as the sorbent in mixed matrix membranes (MMMs). These MOF-based MMMs exhibit high efficiency and selectivity in both static and dynamic regimes in the removal of Hg2+ from aqueous environments, due to the high density of thioalkyl groups decorating MOF channels. Both MMMs are capable to reduce different concentration of the pollutant to …

Mixed matrixMaterials scienceGroundwater remediationchemistry.chemical_element02 engineering and technology010402 general chemistryAigua potable Depuració01 natural sciencesBiomaterialscapture devicemercury(II)ElectrochemistryMaterialsmetal-organic frameworksfungiwater remediation021001 nanoscience & nanotechnologyCondensed Matter Physics6. Clean water0104 chemical sciencesElectronic Optical and Magnetic MaterialsMercury (element)MembranechemistryChemical engineeringMetal-organic frameworkmixed matrix membranes0210 nano-technology
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A Biocompatible Aspartic-Decorated Metal–Organic Framework with Tubular Motif Degradable under Physiological Conditions

2021

Achieving a precise control of the final structure of metal–organic frameworks (MOFs) is necessary to obtain desired physical properties. Here, we describe how the use of a metalloligand design strategy and a judicious choice of ligands inspired from nature is a versatile approach to succeed in this challenging task. We report a new porous chiral MOF, with the formula Ca5II{CuII10[(S,S)-aspartamox]5}·160H2O (1), constructed from Cu2+ and Ca2+ ions and aspartic acid-decorated ligands, where biometal Cu2+ ions are bridged by the carboxylate groups of aspartic acid moieties. The structure of MOF 1 reveals an infinite network of basket-like cages, built by 10 crystallographically distinct Cu(II…

Models MolecularBiocompatibilityMetal ions in aqueous solutionBiocompatible Materials010402 general chemistry01 natural sciencesArticleInorganic Chemistrychemistry.chemical_compoundAdsorptionAspartic acidTumor Cells CulturedHumansCarboxylatePhysical and Theoretical ChemistryMetal-Organic Frameworkschemistry.chemical_classificationAspartic AcidMolecular Structure010405 organic chemistryCombinatorial chemistry0104 chemical sciencesAmino acidchemistryMetal-organic frameworkDrug carrierInorganic Chemistry
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Magnesium Exchanged Zirconium Metal−Organic Frameworks with Improved Detoxification Properties of Nerve Agents

2019

UiO-66, MOF-808 and NU-1000 metal-organic frameworks exhibit a differentiated reactivity toward [Mg(OMe)2(MeOH)2]4 related to their pore accessibility. Microporous UiO-66 remains unchanged while mesoporous MOF-808 and hierarchical micro/mesoporous NU-1000 materials yield doped systems containing exposed MgZr5O2(OH)6 clusters in the mesoporous cavities. This modification is responsible for a remarkable enhancement of the catalytic activity toward the hydrolytic degradation of P-F and P-S bonds of toxic nerve agents, at room temperature, in unbuffered aqueous solutions.

Models MolecularSurface PropertiesQuímica organometàl·licachemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysisColloid and Surface ChemistryPolymer chemistryReactivity (chemistry)MagnesiumParticle SizeMaterialsMetal-Organic FrameworksZirconiumAqueous solutionMagnesiumHydrolysisTemperatureGeneral ChemistryMicroporous material0104 chemical scienceschemistryMetal-organic frameworkZirconiumMesoporous materialNerve AgentsOxidation-ReductionPorosity
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Controlling the molecular diffusion in MOFs with the acidity of monocarboxylate modulators.

2021

The catalytic performance of metal-organic frameworks (MOFs) is related to their physicochemical properties, such as particle size, defect-chemistry and porosity, which synthetic control can be potentially achieved by coordination modulation. By combining PXRD, 1HNMR, FT-IR, N2 uptake measurements we have found insights that the different types of defects (missing linker or missing clusters consequence of the spatial distribution of missing linkers, and the combination of both) could be controlled by the type of modulator employed. We show that the molar percent of defects, either as missing linkers or as part of missing cluster defects, is related to the modulator’s acidity and subse…

Molecular diffusionMetal-Organic Frameworks Defects Coordination modulation Heterogeneous Catalysis010405 organic chemistryChemistry010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisInorganic ChemistryChemical engineeringCluster (physics)Particle sizePorosityMesoporous materialLinkerPowder diffractionDalton transactions (Cambridge, England : 2003)
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Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework

2020

[EN] The exact chemical structure of non-crystallising natural products is still one of the main challenges in Natural Sciences. Despite tremendous advances in total synthesis, the absolute structural determination of a myriad of natural products with very sensitive chemical functionalities remains undone. Here, we show that a metal-organic framework (MOF) with alcohol-containing arms and adsorbed water, enables selective hydrolysis of glycosyl bonds, supramolecular order with the so-formed chiral fragments and absolute determination of the organic structure by single-crystal X-ray crystallography in a single operation. This combined strategy based on a biomimetic, cheap, robust and multigr…

Multidisciplinary010405 organic chemistryChemistryChemical structureScienceQSupramolecular chemistryAbsolute configurationGeneral Physics and AstronomyTotal synthesisGeneral ChemistryMetal-organic frameworks010402 general chemistry01 natural sciencesCombinatorial chemistryGeneral Biochemistry Genetics and Molecular BiologyArticle0104 chemical sciencesCatalysisHydrolysisHydrolaseBiocatalysisMoleculelcsh:Qlcsh:ScienceNature Communications
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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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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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