Search results for "Química organometàl·lica"

showing 10 items of 36 documents

Multivariate Metal-Organic Frameworks for the Simultaneous Capture of Organic and Inorganic Contaminants from Water

2019

We report a new water-stable multivariate (MTV) Metal-Organic Framework (MOF) prepared by combining two different oxamide-based metalloligands derived from the natural amino acids L-serine and L-methionine. This unique material features hexagonal channels decorated with two types of flexible and functional 'arms' (-CH2OH and -CH2CH2SCH3) capable to act, synergistically, for the simultaneous and efficient removal of both inorganic (heavy metals like Hg2+, Pb2+ and Tl+) and organic (dyes such as Pyronin Y, Auramine O, Brilliant Green and Methylene Blue) contaminants and, in addition, this MTV-MOF is completely reusable. Single-crystal X-ray diffraction (SCXRD) measurements allowed to solve th…

Aigua ContaminacióAuramine OChemistryOxamideInorganic chemistryfungiQuímica organometàl·licaHeavy metalsGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryBrilliant greenInorganic contaminantsMetal-organic frameworkMethylene blue
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Magnetic functionalities in MOFs: from the framework to the pore

2017

In this review, we show the different approaches so far developed to prepare Metal-Organic Frameworks (MOFs) presenting electronic functionalities, with particular attention to magnetic properties. We will cover the chemical design of the framework necessary for the incorporation of different magnetic phenomena, as well as the encapsulation of functional species in the pores leading to hybrid multifunctional MOFs combining an extended lattice with a molecular lattice.

Camps magnèticsMaterials scienceQuímica organometàl·licaNanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesEncapsulation (networking)Magnetic PhenomenaLattice (order)0210 nano-technologyChemical designChemical Society Reviews
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Homochiral Metal-Organic Frameworks for Enantioselective Separations in Liquid Chromatography

2020

Selective separation of enantiomers is a substantial challenge for the pharmaceutical industry. Chromatography on chiral stationary phases is the standard method, but at a very high cost for industrial-scale purification due to the high cost of the chiral stationary phases. Typically, these materials are poorly robust, expensive to manufacture, and often too specific for a single desired substrate, lacking desirable versatility across different chiral analytes. Here, we disclose a porous, robust homochiral metal–organic framework (MOF), TAMOF-1, built from copper(II) and an affordable linker prepared from natural l-histidine. TAMOF-1 has shown to be able to separate a variety of model…

ChromatographyMolecular StructureChemistryIndustrial scaleEnantioselective synthesisQuímica organometàl·licaWaterStereoisomerismStereoisomerismGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryHigh-performance liquid chromatography54Catalysis0104 chemical sciencesColloid and Surface ChemistryMoleculeWater chemistryMetal-organic frameworkEnantiomerChromatography High Pressure LiquidCopperMetal-Organic Frameworks
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Pauson-Khand reaction of internal dissymmetric trifluoromethyl alkynes. Influence of the alkene on the regioselectivity.

2014

Abstract: The scope of the Pauson-Khand reaction (PKR) of internal trifluoromethyl alkynes, previously described with norbornadiene, is expanded to norbornene and ethylene. A thorough structural analysis of the resulting PK adducts has been carried out to unveil that α-trifluoromethylcyclopentenones are preferred in all cases, independently of the electronic properties of the alkyne. The regioselectivity observed with norbornadiene and ethylene is higher than in the case of norbornene.

Ciclització (Química)EthyleneHydrocarbons FluorinatedStereochemistryNorbornadieneQuímica organometàl·licaPharmaceutical ScienceAlkynetrifluoromethylalkynesCrystallography X-RayArticlecyclopentenonesAnalytical ChemistryRing formation (Chemistry)cycloadditionslcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryPhysical and Theoretical ChemistryNorbornenechemistry.chemical_classificationPauson-Khand reactionTrifluoromethylMolecular StructureAlkenePauson–Khand reactionOrganic ChemistryRegioselectivityStereoisomerismCobaltEthylenesNorbornaneschemistryOrganometallic chemistryChemistry (miscellaneous)AlkynesregioselectivityMolecular MedicineMolecules (Basel, Switzerland)
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Controlling magnetism with light in zero orbital angular momentum antiferromagnet

2023

Antiferromagnetic materials feature intrinsic ultrafast spin dynamics, making them ideal candidates for future magnonic devices operating at THz frequencies. A major focus of current research is the investigation of optical methods for the efficient generation of coherent magnons in antiferromagnetic insulators. In magnetic lattices endowed with orbital angular momentum, spin-orbit coupling enables spin dynamics through the resonant excitation of low-energy electric dipoles such as phonons and orbital resonances which interact with spins. However, in magnetic systems with zero orbital angular momentum, microscopic pathways for the resonant and low-energy optical excitation of coherent spin …

Condensed Matter - Other Condensed MatterCondensed Matter - Materials ScienceUltrafast Spectroscopy of Correlated MaterialsSpectroscopy of Solids and InterfacesQuímica organometàl·licaGeneral Physics and AstronomyMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesCondensed Matter::Strongly Correlated ElectronsMaterialsOther Condensed Matter (cond-mat.other)
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Bottom‐Up Fabrication of Semiconductive Metal-Organic Framework Ultrathin Films

2018

Though generally considered insulating, recent progress on the discovery of conductive porous metal-organic frameworks (MOFs) offers new opportunities for their integration as electroactive components in electronic devices. Compared to classical semiconductors, these metal-organic hybrids combine the crystallinity of inorganic materials with easier chemical functionalization and processability. Still, future development depends on the ability to produce high-quality films with fine control over their orientation, crystallinity, homogeneity, and thickness. Here self-assembled monolayer substrate modification and bottom-up techniques are used to produce preferentially oriented, ultrathin, con…

FabricationMaterials sciencebusiness.industryMechanical EngineeringQuímica organometàl·licaNanotechnologySelf-assembled monolayer02 engineering and technologyConductivitat elèctrica010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCrystallinitySemiconductorMechanics of MaterialsMonolayerGeneral Materials ScienceMetal-organic framework0210 nano-technologybusinessPorosityElectrical conductor
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Chemical Design and Magnetic Ordering in Thin Layers of 2D Metal–Organic Frameworks (MOFs)

2021

Through rational chemical design, and thanks to the hybrid nature of metal−organic frameworks (MOFs), it is possible to prepare molecule-based 2D magnetic materials stable at ambient conditions. Here, we illustrate the versatility of this approach by changing both the metallic nodes and the ligands in a family of layered MOFs that allows the tuning of their magnetic properties. Specifically, the reaction of benzimidazole-type ligands with different metal centers (MII = Fe, Co, Mn, Zn) in a solventfree synthesis produces a family of crystalline materials, denoted as MUV-1(M), which order antiferromagnetically with critical temperatures that depend on M. Furthermore, the incorporation o…

FabricationThin layersChemistryQuímica organometàl·lica02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysisArticle0104 chemical sciencesCrystallinitysymbols.namesakeColloid and Surface ChemistryChemical physicsMagnetsymbolsMoleculeMetal-organic frameworkvan der Waals force0210 nano-technologyMaterialsTopology (chemistry)Journal of the American Chemical Society
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Structural reorganization in a hydrogen-bonded organic framework

2018

Self-recognition of 3,3′,5,5′-azobenzenetetracarboxylic acid drives the formation of a grid-like anionic hydrogen-bonded framework with channels occupied by organic cations. This supramolecular solid is capable of reorganizing its connectivity in the presence of specific guests into a different crystalline architecture by sequential dissolution and recrystallization.

Hydrogen010405 organic chemistryChemistrySupramolecular chemistryQuímica organometàl·licaRecrystallization (metallurgy)chemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesChemical engineeringMaterials ChemistryCristallsDissolution
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Characterization of the laccase-mediated oligomerization of 4-hydroxybenzoic acid

2016

Modifying inert poly(ethersulfone) membranes using laccase has proven to be an environmentally benign and easily applicable process to alter the membrane's surface properties. By this method phenolic acid monomers such as 4-hydroxybenzoic acid are grafted from the membrane surface to make it anti-fouling. In order to enhance the anti-fouling capabilities even further it is important to study the molecular details of this reaction. However, the nature of the products of laccase modification, either on a surface or in solution, has been studied only poorly. In this paper we report the formation of C3–C3′, C3–O and C1–C3′ linked dimers as the first products of the solution-phase laccase-mediat…

Laccase010405 organic chemistryGeneral Chemical EngineeringDimerOrganic ChemistryQuímica organometàl·licaGeneral Chemistry010402 general chemistryReactivitat (Química)01 natural sciencesOrganische Chemie0104 chemical scienceschemistry.chemical_compoundMonomerMembrane4-Hydroxybenzoic acidchemistryPolymerizationOrganic chemistryLigninLife SciencePhenolsVLAGRSC Advances : An international journal to further the chemical sciences
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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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