0000000001301716

AUTHOR

José J. Calvino

showing 7 related works from this author

Selective oxidative dehydrogenation of ethane over SnO2-promoted NiO catalysts

2012

[EN] Ni-Sn-O mixed oxides catalysts have been investigated for the oxidative dehydrogenation of ethane. The catalysts were prepared through the evaporation of aqueous solutions of nickel nitrate and tin oxalate and finally calcined in air at 500 degrees C for 2 h. These materials have been characterized by several techniques (N-2-adsorption, X-ray diffraction, High-Resolution Electron Microscopy, temperature programmed reduction, X-Ray Photoelectron Spectroscopy, Fourier Transformed Infrared Spectroscopy of adsorbed CO and O-18/O-16 isotope exchange). The addition of just a tiny amount of tin highly increases the selectivity to ethylene (from ca. 40% to 80-90%). Thus, high selectivity to et…

SnO2-promotedInorganic chemistrychemistry.chemical_elementInfrared spectroscopyTin oxideCatalysisOxalateCatalysisEthane ODHNiO catalystsEthane oxidationchemistry.chemical_compoundNickelEthyleneTin oxidechemistryDehydrogenationPhysical and Theoretical ChemistryTemperature-programmed reductionTinOxidative dehydrogenation of ethaneNickel oxideCatalyst characterization (XPS HREM oxygen isotope exchange FTIR CO adsorbed)
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Synthesis of Densely Packaged, Ultrasmall Pt02Clusters within a Thioether-Functionalized MOF: Catalytic Activity in Industrial Reactions at Low Tempe…

2018

The gram-scale synthesis, stabilization, and characterization of well-defined ultrasmall subnanometric catalytic clusters on solids is a challenge. The chemical synthesis and X-ray snapshots of Pt02 clusters, homogenously distributed and densely packaged within the channels of a metal-organic framework, is presented. This hybrid material catalyzes efficiently, and even more importantly from an economic and environmental viewpoint, at low temperature (25 to 140 °C), energetically costly industrial reactions in the gas phase such as HCN production, CO2 methanation, and alkene hydrogenations. These results open the way for the design of precisely defined catalytically active ultrasmall metal c…

Materials science02 engineering and technologyHeterogeneous catalysis010402 general chemistryChemical synthesis01 natural sciencesCatalysisCatalysisCatalysimetal–organic frameworkchemistry.chemical_compoundmetal–organic frameworksThioetherMethanationheterogeneous catalysis; metal clusters; metal–organic frameworks; platinum; structural flexibility; Catalysis; Chemistry (all)platinumchemistry.chemical_classificationAlkene010405 organic chemistrystructural flexibilityChemistry (all)General ChemistryGeneral Medicinemetal cluster021001 nanoscience & nanotechnology0104 chemical sciencesheterogeneous catalysismetal clusterschemistryChemical engineeringheterogeneous catalysiMetal-organic framework0210 nano-technologyHybrid material
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Silver Clusters of Five Atoms as Highly Selective Antitumoral Agents Through Irreversible Oxidation of Thiols

2022

Low atomicity clusters present properties dependent on the size, due to the quantum confinement, with well-defined electronic structures and high stability. Here it is shown that Ag5 clusters catalyze the complete oxidation of sulfur to S+6. Ag5 catalytic activity increases with different oxidant species in the order O2 ≪ H2O2 < OH•. Selective oxidation of thiols on the cysteine residues of glutathione and thioredoxin is the primary mechanism human cells have to maintain redox homeostasis. Contingent upon oxidant concentration, Ag5 catalyzes the irreversible oxidation of glutathione and thioredoxin, triggering apoptosis. Modification of the intracellular environment to a more oxidized state…

Cancer therapycatalysissilver clusterssulfur oxidationCondensed Matter PhysicsCatalysisSulfur oxidationElectronic Optical and Magnetic MaterialsBiomaterialsLow atomicity clustersSettore CHIM/03 - Chimica Generale E InorganicaElectrochemistrycancer therapylow atomicity clustersSilver clusters
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Confined Pt-1(1+) Water Clusters in a MOF Catalyze the Low-Temperature Water-Gas Shift Reaction with both CO2 Oxygen Atoms Coming from Water

2018

[EN] The synthesis and reactivity of single metal atoms in a low-valence state bound to just water, rather than to organic ligands or surfaces, is a major experimental challenge. Herein, we show a gram-scale wet synthesis of Pt-1(1+) stabilized in a confined space by a crystallographically well-defined first water sphere, and with a second coordination sphere linked to a metal-organic framework (MOF) through electrostatic and H-bonding interactions. The role of the water cluster is not only isolating and stabilizing the Pt atoms, but also regulating the charge of the metal and the adsorption of reactants. This is shown for the low-temperature water-gas shift reaction (WGSR: CO + H2O CO2 + H…

PhysicsWater–gas shift reactionQuímica Inorgánicabiology010405 organic chemistryWater-gas shift reactionSingle atom catalystGeneral MedicineGeneral ChemistryMetal-organic frameworks010402 general chemistrybiology.organism_classification01 natural sciencesCatalysisWater-gas shift reactionSingle-atom catalyst0104 chemical sciencesOxygen atomWater clustersPhysical chemistryValenciaMetal-organic frameworks (MOFs)Platinum
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CCDC 1587822: Experimental Crystal Structure Determination

2018

Related Article: Marta Mon, Miguel A. Rivero-Crespo, Jesffls Ferrando-Soria, Alejandro Vidal-Moya, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan C. Hernandez-Garrido, Miguel Lopez-Haro, José J. Calvino, Giulio Ragazzon, Alberto Credi, Donatella Armentano, Emilio Pardo|2018|Angew.Chem.,Int.Ed.|57|6186|doi:10.1002/anie.201801957

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[bis((mu-aqua)-tris(mu-2-[(2-{[1-carboxylato-3-(methylsulfanyl)propyl]azanidyl}-1-oxidanidyl-2-oxoethylidene)amino]-4-(methylsulfanyl)butanoato)-bis(mu-hydroxo)-calcium(ii)-hexa-copper(ii)) bis(dichloro-platinum(ii)) di-platinum(0) unknown solvate triacontahydrate]Experimental 3D Coordinates
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CSD 1409698: Experimental Crystal Structure Determination

2018

Related Article: Marta Mon, Miguel A. Rivero-Crespo, Jesffls Ferrando-Soria, Alejandro Vidal-Moya, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan C. Hernandez-Garrido, Miguel Lopez-Haro, José J. Calvino, Giulio Ragazzon, Alberto Credi, Donatella Armentano, Emilio Pardo|2018|Angew.Chem.,Int.Ed.|57|6186|doi:10.1002/anie.201801957

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1587821: Experimental Crystal Structure Determination

2018

Related Article: Marta Mon, Miguel A. Rivero-Crespo, Jesffls Ferrando-Soria, Alejandro Vidal-Moya, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan C. Hernandez-Garrido, Miguel Lopez-Haro, José J. Calvino, Giulio Ragazzon, Alberto Credi, Donatella Armentano, Emilio Pardo|2018|Angew.Chem.,Int.Ed.|57|6186|doi:10.1002/anie.201801957

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[(mu-aqua)-tris(mu-2-{[{[1-azanidylidene-4-(methylsulfanyl)-1-oxidobutan-2-yl]oxy}(oxo)acetyl]azanidyl}-4-(methylsulfanyl)butanoato)-bis(mu-hydroxo)-calcium(ii)-hexa-copper(ii) bis(dichloro-platinum(ii)) unknown solvate tridecahydrate]Experimental 3D Coordinates
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