2024
Tuning Metal–Organic Framework Linker Chemistry for Transition Metal Ion Separations
Violet C, Parkinson M, Ball A, Kulik H, Fortner J, Elimelech M. Tuning Metal–Organic Framework Linker Chemistry for Transition Metal Ion Separations. ACS Applied Materials & Interfaces 2024, 17: 1911-1921. PMID: 39682030, DOI: 10.1021/acsami.4c16173.Peer-Reviewed Original ResearchMetal-organic frameworksUiO-66-XTransition metal ionsIon separationMetal ionsSolvent-assisted linker exchangeParent metal-organic frameworkDensity functional theory calculationsFunctional groupsBinding energyUiO-66-(COOH)<sub>2</subIon binding energiesMetal ion separationUiO-66-COOHUiO-66 derivativesLinker chemistryPost-synthetic modificationCarboxylic acid groupsIncorporation of carboxylic acid groupsQuartz crystal microbalanceLinker exchangeUiO-66Pore windowsHigh selectivityMaterials chemistry
2008
Acetylacetonate Anchors for Robust Functionalization of TiO2 Nanoparticles with Mn(II)−Terpyridine Complexes
McNamara WR, Snoeberger RC, Li G, Schleicher JM, Cady CW, Poyatos M, Schmuttenmaer CA, Crabtree RH, Brudvig GW, Batista VS. Acetylacetonate Anchors for Robust Functionalization of TiO2 Nanoparticles with Mn(II)−Terpyridine Complexes. Journal Of The American Chemical Society 2008, 130: 14329-14338. PMID: 18831585, DOI: 10.1021/ja805498w.Peer-Reviewed Original ResearchMeSH KeywordsComputer SimulationElectron Spin Resonance SpectroscopyElectronsHydroxybutyratesLightManganeseMembranes, ArtificialModels, ChemicalModels, MolecularMolecular StructureNanoparticlesOrganometallic CompoundsOxidation-ReductionParticle SizePentanonesPhotochemistryPorosityPyridinesSensitivity and SpecificitySpectrophotometry, UltravioletSurface PropertiesTime FactorsTitaniumWaterConceptsInterfacial electron injectionTiO2 nanoparticlesRobust functionalizationTransition metal ionsVisible light sensitizationElectron injectionInterfacial electron transferColloidal thin filmsTerpy complexesPhotocatalytic complexesOxidation chemistryEffective catalystCoupling reactionElectron transferNanoparticlesVariety of scaffoldsComplex of caPhotovoltaic devicesFunctionalizationSubpicosecond time scaleAqueous suspensionOxidative conditionsThin filmsComplexesTransient measurements
2005
Advanced Glycosylation of LDL: Role in Oxidative Modification and Diabetic Complications
Bucala R, Makita Z, Cerami A, Vlassara H, Koschinsky T. Advanced Glycosylation of LDL: Role in Oxidative Modification and Diabetic Complications. 2005, 286-291. DOI: 10.1533/9781845698393.4.286.Peer-Reviewed Original ResearchTransition metal ionsAmine-containing phospholipidsRedox reactionsMetal ionsFree metalFacile mechanismOxidative modificationOxidationLipid oxidationApoprotein componentsMoietyGlycosylationAcid oxidationIonsAbsorbanceReactionModificationMetalsAGE moietiesFluorescencePhospholipidsPropertiesAdvanced glycosylationImmunochemical propertiesFormation
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