0000000000424220

AUTHOR

María Romero-angel

0000-0002-0365-8209

showing 3 related works from this author

Surfactant-assisted synthesis of titanium nanoMOFs for thin film fabrication

2021

We use dodecanoic acid as a modulator to yield titanium MOF nanoparticles with good control of size and colloid stability and minimum impact to the properties of the framework to enable direct fabrication of crystalline, porous thin films. ispartof: CHEMICAL COMMUNICATIONS vol:57 issue:72 pages:9040-9043 ispartof: location:England status: published

FabricationYield (engineering)Materials scienceChemistry MultidisciplinaryNanoparticlechemistry.chemical_elementGood control02 engineering and technology010402 general chemistry01 natural sciencesCatalysisMETAL-ORGANIC FRAMEWORKSColloidPulmonary surfactantMaterials ChemistryThin filmScience & Technologytechnology industry and agricultureMetals and AlloysGeneral Chemistryequipment and supplies021001 nanoscience & nanotechnologyeye diseases0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemistrySIZEchemistryChemical engineeringPhysical SciencesACIDCeramics and CompositesNH2-MIL-125(TI)sense organs0210 nano-technologyTitaniumChemical Communications
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Heterometallic Titanium-Organic Frameworks as Dual Metal Catalysts for Synergistic Non-Buffered Hydrolysis of Nerve Agent Simulants

2020

Heterometallic metal-organic frameworks (MOFs) can offer important advantages over their homometallic counterparts to enable targeted modification of their adsorption, structural response, electronic structure, or chemical reactivity. However, controlling metal distribution in these solids still remains a challenge. The family of mesoporous titanium-organic frameworks, MUV-101(M), displays heterometallic TiM2 nodes assembled from direct reaction of Ti(IV) and M(II) salts. We use the degradation of nerve agent simulants to demonstrate that only TiFe2 nodes are capable of catalytic degradation in non-buffered conditions. By using an integrative experimental-computational approach, we rational…

General Chemical Engineeringchemistry.chemical_element02 engineering and technology010402 general chemistryHeterogeneous catalysis01 natural sciencesBiochemistryCatalysisMetalchemistry.chemical_compoundHydrolysisMaterials ChemistryEnvironmental ChemistrySynergistic catalysisLewis acids and basesBimetallic stripBiochemistry (medical)General ChemistryPurple acid phosphatases021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryvisual_artvisual_art.visual_art_mediumChemical stabilityTrimesic acid0210 nano-technologyBrønsted–Lowry acid–base theoryTitanium
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Hydroxamate Titanium–Organic Frameworks and the Effect of Siderophore-Type Linkers over Their Photocatalytic Activity

2019

The chemistry of metal–organic frameworks (MOFs) relies on the controlled linking of organic molecules and inorganic secondary building units to assemble an unlimited number of reticular frameworks. However, the design of porous solids with chemical stability still remains limited to carboxylate or azolate groups. There is a timely opportunity to develop new synthetic platforms that make use of unexplored metal binding groups to produce metal–linker joints with hydrolytic stability. Living organisms use siderophores (iron carriers in Greek) to effectively assimilate iron in soluble form. These compounds make use of hard oxo donors as hydroxamate or catecholate groups to coordinate metal Lew…

SiderophoreQuímica organometàl·licachemistry.chemical_elementGeneral ChemistryTitani010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisMetalchemistry.chemical_compoundColloid and Surface Chemistrychemistryvisual_artvisual_art.visual_art_mediumPhotocatalysisChemical stabilityLewis acids and basesCarboxylateTitaniumJournal of the American Chemical Society
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