0000000000249674

AUTHOR

Christian W. Lopes

0000-0001-8420-1958

showing 6 related works from this author

Use of alkylarsonium directing agents for the synthesis and study of zeolites

2019

[EN] Expanding the previously known family of -onium (ammonium, phosphonium, and sulfonium) organic structure-directing agents (OSDAs) for the synthesis of zeolite MFI, a new member, the arsonium cation, is used for the first time. The new group of tetraalkylarsonium cations has allowed the synthesis of the zeolite ZSM-5 with several different chemical compositions, opening a route for the synthesis of zeolites with a new series of OSDA. Moreover, the use of As replacing N in the OSDA allows the introduction of probe atoms that facilitate the study of these molecules by powder X-ray diffraction (PXRD), solid-state nuclear magnetic resonance (MAS NMR), and X-ray absorption spectroscopy (XAS)…

X-ray absorption spectroscopyChemistrySulfoniumOrganic ChemistryGeneral ChemistryOniumAlkylarsoniumCatalysislaw.inventionArsenicchemistry.chemical_compoundCrystallographyCompostos orgànics SíntesiStructure-directing agentslawCationsQUIMICA ANALITICAZeolitesMoleculePhosphoniumCrystallizationZeoliteMaterialsPowder diffraction
researchProduct

MOF-Mediated Synthesis of Supported Fe-Doped Pd Nanoparticles under Mild Conditions for Magnetically Recoverable Catalysis**

2020

Metal–organic framework (MOF)-driven synthesis is considered as a promising alternative for the development of new catalytic materials with well-designed active sites. This synthetic approach is used here to gradually transform a new bimetallic MOF, with Pd and Fe as the metal components, by the in situ generation of aniline under mild conditions. This methodology results in a compositionally homogeneous nanocomposite formed by Fe-doped Pd nanoparticles that, in turn, are supported on iron oxide-doped carbon. The nanocomposite has been fully characterized by several techniques such as IR and Raman spectroscopy, TEM, XPS, and XAS. The performance of this nanocomposite as an heterogeneous cat…

Materials scienceIron09.- Desarrollar infraestructuras resilientes promover la industrialización inclusiva y sostenible y fomentar la innovaciónNanoparticle010402 general chemistryHeterogeneous catalysis01 natural sciences7. Clean energyCatalysisCatalysisNitrobenzenechemistry.chemical_compoundLight sourceAnilineCatàlisiQUIMICA ANALITICAmedia_common.cataloged_instanceUser FacilityEuropean unionBimetallic stripmedia_commonX-ray absorption spectroscopyNanocomposite010405 organic chemistryOrganic ChemistryGeneral ChemistryMetal-organic frameworks0104 chemical sciences12.- Garantizar las pautas de consumo y de producción sostenibleschemistryChemical engineeringFe dopedPd nanoparticlesNanoparticlesMaterials nanoestructuratsNational laboratoryHumanitiesPalladium
researchProduct

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
researchProduct

CCDC 1910863: Experimental Crystal Structure Determination

2019

Related Article: Sara Sáez-Ferre, Christian W. Lopes, Jorge Simancas, Alejandro Vidal-Moya, Teresa Blasco, Giovanni Agostini, Guillermo Mínguez Espallargas, Jose L. Jordá, Fernando Rey, Pascual Oña-Burgos|2019|Chem.-Eur.J.|25|16390|doi:10.1002/chem.201904043

Space GroupCrystallographytetraethylarsanium iodide sesquihydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 1841391: Experimental Crystal Structure Determination

2018

Related Article: Miguel A. Rivero-Crespo, Marta Mon, Jesús Ferrando-Soria, Christian W. Lopes, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan C. Hernández-Garrido, Miguel López-Haro, Jose J. Calvino, Enrique V. Ramos-Fernandez, Donatella Armentano, Emilio Pardo|2018|Angew.Chem.,Int.Ed.|57|17094|doi:10.1002/anie.201810251

Space GroupCrystallographycatena-[tetra-aqua-platinum(i) tri-sodium (mu-oxo)-dihydroxy-tetra-ammine-di-platinum(ii) bis(tris(mu-24-bis((carboxylato(oxidanidyl)methylidene)amino)-135-trimethylbenzene)-tetra-aqua-tri-copper(ii)-di-nickel(ii)) heptahexacontahydrate]Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 1841392: Experimental Crystal Structure Determination

2018

Related Article: Miguel A. Rivero-Crespo, Marta Mon, Jesús Ferrando-Soria, Christian W. Lopes, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan C. Hernández-Garrido, Miguel López-Haro, Jose J. Calvino, Enrique V. Ramos-Fernandez, Donatella Armentano, Emilio Pardo|2018|Angew.Chem.,Int.Ed.|57|17094|doi:10.1002/anie.201810251

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatescatena-[(mu-aqua)-hexaammine-di-platinum(ii) tetraammine-platinum(ii) hexakis(mu-24-bis{[carboxylato(oxidanidyl)methylidene]amino}-135-trimethylbenzene)-hexa-copper(ii)-tetra-nickel(ii) pentahexacontahydrate]
researchProduct