0000000001300121

AUTHOR

Jorge Gascon

showing 27 related works from this author

Unlocking mixed oxides with unprecedented stoichiometries from heterometallic metalorganic frameworks for the catalytic hydrogenation of CO 2

2021

[EN] Their complex surface chemistry and high oxygen lattice mobilities place mixed-metal oxides among the most important families of materials. Modulation of stoichiometry in mixed-metal oxides has been shown to be a very powerful tool for tuning optical and catalytic properties. However, accessing different stoichiometries is not always synthetically possible. Here, we show that the thermal decomposition of the recently reported metal-organic framework MUV-101(Fe, Ti) results in the formation of carbon-supported titanomaghemite nanoparticles with an unprecedented Fe/Ti ratio close to 2, not achievable by soft-chemistry routes. The resulting titanomaghemite phase displays outstanding catal…

titanomaghemiteMaterials scienceRWGSNanoparticle02 engineering and technology010402 general chemistry01 natural sciencesReverse water-gas shiftWater-gas shift reactionMixed oxidesCatalysisTitanomaghemitePhase (matter)[CHIM.CRIS]Chemical Sciences/CristallographyPhysical and Theoretical Chemistrymixed oxidesOrganic ChemistryThermal decomposition[CHIM.MATE]Chemical Sciences/Material chemistry[CHIM.CATA]Chemical Sciences/Catalysis021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringChemistry (miscellaneous)reverse water-gas shiftMetal-organic framework0210 nano-technologySelectivityMOF-mediated synthesisStoichiometry
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PBI mixed matrix hollow fiber membrane: Influence of ZIF-8 filler over H2/CO2 separation performance at high temperature and pressure

2020

High performance and commercially attractive mixed-matrix membranes were developed for H2/CO2 separation via a scalable hollow fiber spinning process. Thin (~300 nm) and defect-free selective layers were successfully created with a uniform distribution of the nanosized (~60 nm) zeolitic-imidazole framework (ZIF-8) filler within the polymer (polybenzimidazole, PBI) matrix. These membranes were able to operate at high temperature (150 °C) and pressure (up to 30 bar) process conditions required in treatment of pre-combustion and syngas process gas streams. Compared with neat PBI hollow fibers, filler incorporation into the polymer matrix leads to a strong increase in H2 permeance from 65 GPU t…

Materials scienceFiltration and Separation02 engineering and technologyPermeance021001 nanoscience & nanotechnologyCO2 capturePre-combustionH2/CO2 separationH/CO separationAnalytical ChemistryAdsorptionMembrane020401 chemical engineeringChemical engineeringHollow fiber membraneMixed matrix membraneGas separationFiber0204 chemical engineering0210 nano-technologyCO captureHollow fiber spinningSyngasBar (unit)
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Cation influence in adsorptive propane/propylene separation in ZIF-8 (SOD) topology

2019

Separation of propylene/propane is one of the most challenging and energy consuming processes in the chemical industry. Propylene demand is increasing and a 99.5% purity is required for industrial purposes. Adsorption based solutions are the most promising alternatives to improve the economical/energetic efficiency of the process. Zeolitic Imidazolate Frameworks (ZIFs) combine the desired characteristics from both MOFs and zeolites: tunability and flexibility from metal organic frameworks, and exceptional thermal and chemical stability from zeolites. In order to enlighten the role of the cation in the sodalite ZIF-8 framework for propane/propylene separation, dynamic breakthrough measuremen…

Materials scienceSolucions polimèriquesGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesIndustrial and Manufacturing EngineeringSeparationchemistry.chemical_compoundAdsorptionPropaneEnvironmental ChemistrySelective gas adsorptionMaterialschemistry.chemical_classificationZeolitic Imidazolate Framework (ZIFs)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesZIF-67HydrocarbonchemistryChemical engineeringMUV-3Chemical stabilityMetal-organic framework0210 nano-technologySelectivityZIF-8CobaltZeolitic imidazolate frameworkChemical Engineering Journal
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The oxamate route, a versatile post-functionalization for metal incorporation in MIL-101(Cr): Catalytic applications of Cu, Pd, and Au

2013

Abstract A new consecutive post-functionalization method has been developed for the inclusion of additional metal functionalities in Metal Organic Frameworks (MOFs) through oxamate as chelating agent. This may result in catalytic centers of metal–organic complexes or in controlled formation of metal nanoparticles, demonstrated for Cu, Pd and Au, in the highly stable MIL-101(Cr) framework. In a first post-synthesis step, reduction of the NO 2 -MIL-101(Cr) leads to the formation of NH 2 -MIL-101(Cr). The second functionalization consists of a straightforward condensation of the amino groups of the ligand with ethyl chloro-oxoacetate resulting in the formation of free oxamates attached to the …

Heterogeneous catalysisChemistryInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisCopperPost-functionalizationCatalysisCoupling reactionCatalysisMetalMetal complexMetal organic frameworkColloidal goldNH2-MIL-101(Cr)visual_artvisual_art.visual_art_mediumNanoparticlesMetal-organic frameworkOxamateGoldPhysical and Theoretical ChemistryPalladiumCopperPalladium
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The MOF-driven synthesis of supported palladium clusters with catalytic activity for carbene-mediated chemistry

2016

The development of catalysts able to assist industrially important chemical processes is a topic of high importance. In view of the catalytic capabilities of small metal clusters, research efforts are being focused on the synthesis of novel catalysts bearing such active sites. Here we report a heterogeneous catalyst consisting of Pd4 clusters with mixed-valence 0/+1 oxidation states, stabilized and homogeneously organized within the walls of a metal-organic framework (MOF). The resulting solid catalyst outperforms state-of-the-art metal catalysts in carbene-mediated reactions of diazoacetates, with high yields (>90%) and turnover numbers (up to 100,000). In addition, the MOF-supported Pd4 c…

Chemical processMechanical Engineeringchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsHeterogeneous catalysis01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryMechanics of MaterialsOrganic chemistryGeneral Materials ScienceMetal catalyst0210 nano-technologyCarbenePalladiumMetal clustersNature Materials
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Insights into the Dynamics of Grotthuss Mechanism in a Proton-Conducting Chiral bioMOF

2016

Proton conduction in solids attracts great interest, not only because of possible applications in fuel cell technologies, but also because of the main role of this process in many biological mechanisms. Metal–organic frameworks (MOFs) can exhibit exceptional proton-conduction performances, because of the large number of hydrogen-bonded water molecules embedded in their pores. However, further work remains to be done to elucidate the real conducting mechanism. Among the different MOF subfamilies, bioMOFs, which have been constructed using biomolecule derivatives as building blocks and often affording water-stable materials, emerge as valuable systems to study the transport mechanisms involve…

chemistry.chemical_classificationMaterials scienceProtonGeneral Chemical EngineeringBiomoleculeNanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistryMaterials ChemistryMoleculeFuel cellsGrotthuss mechanism0210 nano-technologyPorosityChemistry of Materials
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Fe-MOF Materials as Precursors for the Catalytic Dehydrogenation of Isobutane.

2022

We investigate the use of a series of iron-based metal–organic frameworks as precursors for the manufacturing of isobutane dehydrogenation catalysts. Both the as-prepared and spent catalysts were characterized by PXRD, XPS, PDF, ICP-OES, and CHNS+O to determine the physicochemical properties of the materials and the active phases responsible for the catalytic activity. In contrast to the previous literature, our results indicate that (i) the formation of metallic Fe under reaction conditions results in secondary cracking and coke formation; (ii) the formation of iron carbide only contributes to coke formation; and (iii) the stabilization of the Fe2+ species is paramount to achieve sta…

General ChemistryQuímicaCatalysis
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Highly selective chemical sensing in a luminescent nanoporous magnet.

2012

Among the wide variety of properties of interest that a given material can exhibit, luminescence is attracting an increasing attention due to its potential application in optical devices for lighting equipment and optical storage, [ 1a − c] optical switching, [ 1d ,e] and sensing. [ 1f − i ] At this respect, many scientists, working in the multidisciplinary fi eld of the materials science, have directed their efforts to the obtention of luminescent materials with potential sensing applications. For instance, sensitive and selective detection of gas and vapor phase analytes can result specially interesting because of the variety of applications that can be found in many different fi elds. A …

FabricationMaterials scienceNanotechnologyOptical storagePhotochemistryOptical switchNanoporesMolecular recognitionGeneral Materials ScienceManganesebusiness.industryNanoporousMechanical EngineeringMolecular electronicsCarbon DioxideSpectrometry FluorescenceMechanics of MaterialsMagnetsSolventsQuantum TheoryMetal-organic frameworkAdsorptionGasesPhotonicsbusinessMethaneCopperAdvanced materials (Deerfield Beach, Fla.)
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Postsynthetic Improvement of the Physical Properties in a Metal-Organic Framework through a Single Crystal to Single Crystal Transmetallation

2015

As ingle crystal to single crystal transmetallation process takes place in the three-dimensional (3D) metal- organic framework (MOF) of formula Mg II 2{Mg II 4(Cu II 2- (Me3mpba)2)3}·45 H2 O( 1 ;M e 3mpba 4¢ = N,N'-2,4,6-trimethyl- 1,3-phenylenebis(oxamate)). After complete replacement of the Mg II ions within the coordination network and those hosted in the channels by either Co II or Ni II ions, 1 is transmetallated to yield two novel MOFs of formulae Co2 II {Co II 4(Cu II 2(Me3- mpba)2)3}·56 H2 O( 2 )a nd Ni2 II {Ni II 4(Cu II 2(Me3mpba)2)3}· 54 H2 O( 3). This unique postsynthetic metal substitution affords materials with higher structural stability leading to enhanced gas sorption and m…

ChemistryLigandStereochemistryMetal ions in aqueous solutionSupramolecular chemistryGeneral MedicineGeneral ChemistryCatalysisMetalCrystalTransmetalationCrystallographyvisual_artYield (chemistry)visual_art.visual_art_mediumSingle crystalAngewandte Chemie International Edition
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Cover Picture: Solid-State Molecular Nanomagnet Inclusion into a Magnetic Metal-Organic Framework: Interplay of the Magnetic Properties (Chem. Eur. J…

2015

ChemistryOrganic ChemistrySolid-stateMetal-organic frameworkNanotechnologyCover (algebra)General ChemistryInclusion (mineral)NanomagnetCatalysisChemistry - A European Journal
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Selective Gas and Vapor Sorption and Magnetic Sensing by an Isoreticular Mixed-Metal–Organic Framework

2012

A novel isoreticular oxamato-based manganese(II)-copper(II) open metal-organic framework H(2)O@iso1 featuring a pillared square/octagonal layer structure with alternating open and closed octagonal pores has been rationally prepared. The open-framework topology is responsible for a large selectivity in the separation of small gas (CO(2) over CH(4)) and vapor molecules (CH(3)OH over CH(3)CN and CH(3)CH(2)OH). H(2)O@iso1 displays a long-range three-dimensional ferromagnetic ordering with a drastic variation of the critical temperature as a function of the guest molecule [T(C)2.0 K (CO(2)@iso1 and CH(4)@iso1) and T(C) = 6.5 (CH(3)OH@iso1) and 21.0 K (H(2)O@iso1)].

Mixed metalChemistryInorganic chemistrychemistry.chemical_elementSorptionGeneral ChemistryManganeseBiochemistryCatalysisColloid and Surface ChemistryFerromagnetismMoleculePhysical chemistrySelectivityLayer (electronics)Topology (chemistry)Journal of the American Chemical Society
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Solid-State Molecular Nanomagnet Inclusion into a Magnetic Metal-Organic Framework: Interplay of the Magnetic Properties.

2015

Single-ion magnets (SIMs) are the smallest possible magnetic devices and are a controllable, bottom-up approach to nanoscale magnetism with potential applications in quantum computing and high-density information storage. In this work, we take advantage of the promising, but yet insufficiently explored, solid-state chemistry of metal-organic frameworks (MOFs) to report the single-crystal to single-crystal inclusion of such molecular nanomagnets within the pores of a magnetic MOF. The resulting host-guest supramolecular aggregate is used as a playground in the first in-depth study on the interplay between the internal magnetic field created by the long-range magnetic ordering of the structur…

010405 organic chemistryMagnetismChemistryOrganic ChemistrySupramolecular chemistryPhysics::OpticsNanotechnologyGeneral Chemistry010402 general chemistry01 natural sciencesNanomagnetCatalysis0104 chemical sciencesMagnetic fieldMagnetMetal-organic frameworkNanoscopic scaleQuantum computerChemistry (Weinheim an der Bergstrasse, Germany)
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Tuning the selectivity of light hydrocarbons in natural gas in a family of isoreticular MOFs

2017

Purification of methane from other light hydrocarbons in natural gas is a topic of intense research due to its fundamental importance in the utilization of natural gas fields. Porous materials have emerged as excellent alternative platforms to conventional cryogenic methodologies to perform this task in a cost- and energy-efficient manner. Here we report a new family of isoreticular chiral MOFs, prepared from oxamidato ligands derived from natural amino acids L-alanine, L-valine and L-leucine, where, by increasing the length of the alkyl residue of the amino acid, the charge density of the MOF's channels can be tuned (1 > 2 > 3), decreasing the adsorption preference towards methane over lig…

Inorganic chemistry02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyMethaneIsoreticularchemistry.chemical_compoundAdsorptionLight hydrocarbonsNatural gasGeneral Materials ScienceAlkylchemistry.chemical_classificationQuímica InorgánicaRenewable Energy Sustainability and the Environmentbusiness.industryRational designCharge densityGeneral ChemistryNatural gas021001 nanoscience & nanotechnologyMOFs0104 chemical scienceschemistryChemical engineering13. Climate action0210 nano-technologySelectivityPorous mediumbusiness
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Selective Gold Recovery and Catalysis in a Highly Flexible Methionine-Decorated Metal–Organic Framework

2016

A novel chiral 3D bioMOF exhibiting functional channels with thio-alkyl chains derived from the natural amino acid l-methionine (1) has been rationally prepared. The well-known strong affinity of gold for sulfur derivatives, together with the extremely high flexibility of the thioether "arms" decorating the channels, account for a selective capture of gold(III) and gold(I) salts in the presence of other metal cations typically found in electronic wastes. The X-ray single-crystal structures of the different gold adsorbates Au(III)@1 and Au(I)@1 suggest that the selective metal capture occurs in a metal ion recognition process somehow mimicking what happens in biological systems and protein r…

chemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesBiochemistrySulfurCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryThioetherchemistryvisual_artvisual_art.visual_art_mediumOrganic chemistryMetal-organic framework0210 nano-technologyHybrid materialHydroalkoxylationJournal of the American Chemical Society
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CCDC 1451174: Experimental Crystal Structure Determination

2017

Related Article: Thais Grancha, Jesús Ferrando-Soria, Joan Cano, Pedro Amoros , Beatriz Seoane, Jorge Gascon, Montse Bazaga-García, Enrique R. Losilla, Aurelio Cabeza, Donatella Armentano, Emilio Pardo|2016|Chem.Mater.|28|4608|doi:10.1021/acs.chemmater.6b01286

catena-[tris(mu-NN'-bis((S)-2-propanoato)oxamide)-(mu-aqua)-bis(mu-hydroxy)-calcium(ii)-hexa-copper(ii) hydrate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1530550: Experimental Crystal Structure Determination

2017

Related Article: Thais Grancha, Marta Mon, Jesús Ferrando-Soria, Jorge Gascon, Beatriz Seoane, Enrique V. Ramos-Fernandez, Donatella Armentano, Emilio Pardo|2017|J.Mater.Chem.A|5|11032|doi:10.1039/C7TA01179B

Space GroupCrystallographycatena-[tris(mu-22'-[(12-dioxoethane-12-diyl)bis(azanidediyl)]bis(4-methylpentanoate))-bis(mu-hydroxo)-(mu-aqua)-calcium-hexa-copper unknown solvate undecahydrate]Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1432054: Experimental Crystal Structure Determination

2016

Related Article: Thais Grancha, Jesús Ferrando-Soria, Joan Cano, Pedro Amoros , Beatriz Seoane, Jorge Gascon, Montse Bazaga-García, Enrique R. Losilla, Aurelio Cabeza, Donatella Armentano, Emilio Pardo|2016|Chem.Mater.|28|4608|doi:10.1021/acs.chemmater.6b01286

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatescatena-(tris(mu-22'-((12-dihydroxyethane-12-diylidene)diazanylylidene)dipropanoato)-tris(mu-hydroxo)-calcium-hexa-copper dotriacontahydrate)
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CCDC 1030505: Experimental Crystal Structure Determination

2015

Related Article: Thais Grancha, Jesús Ferrando-Soria, Hong-Cai Zhou, Jorge Gascon, Beatriz Seoane, Jorge Pasán, Oscar Fabelo, Miguel Julve and Emilio Pardo|2015|Angew.Chem.,Int.Ed.|54|6521|doi:10.1002/anie.201501691

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametershexa-nickel bis(mu-24-bis([carboxylato(oxidanidyl)methylidene]amino)-135-trimethylbenzene)-tetra-aqua-di-copper bis(bis(24-bis([carboxylato(oxidanidyl)methylidene]amino)-135-trimethylbenzene)-diaqua-dicopper) nonahydrateExperimental 3D Coordinates
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CCDC 1530549: Experimental Crystal Structure Determination

2017

Related Article: Thais Grancha, Marta Mon, Jesús Ferrando-Soria, Jorge Gascon, Beatriz Seoane, Enrique V. Ramos-Fernandez, Donatella Armentano, Emilio Pardo|2017|J.Mater.Chem.A|5|11032|doi:10.1039/C7TA01179B

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[tris(mu-22'-[(12-dioxoethane-12-diyl)bis(azanidediyl)]bis(4-methylpentanoate))-bis(mu-hydroxo)-(mu-aqua)-calcium-hexa-copper unknown solvate tridecahydrate]Experimental 3D Coordinates
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CCDC 1478222: Experimental Crystal Structure Determination

2016

Related Article: Marta Mon, Jesús Ferrando-Soria, Thais Grancha, Francisco R. Fortea-Pérez, Jorge Gascon, Antonio Leyva-Pérez, Donatella Armentano, and Emilio Pardo|2016|J.Am.Chem.Soc.|138|7864|doi:10.1021/jacs.6b04635

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[tris(mu-2-((2-((1-carboxylato-3-(methylsulfanyl)propyl)amino)-1-oxy-2-oxoethylidene)amino)-4-(methylsulfanyl)butanoato)-bis(mu-hydroxy)-(mu-aqua)-trichloro-calcium(ii)-hexa-copper(ii)-tri-gold(iii) hexakis(chloride) unknown solvate nonahydrate]Experimental 3D Coordinates
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CCDC 1030506: Experimental Crystal Structure Determination

2015

Related Article: Thais Grancha, Jesús Ferrando-Soria, Hong-Cai Zhou, Jorge Gascon, Beatriz Seoane, Jorge Pasán, Oscar Fabelo, Miguel Julve and Emilio Pardo|2015|Angew.Chem.,Int.Ed.|54|6521|doi:10.1002/anie.201501691

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametershexa-cobalt bis(mu-24-bis([carboxylato(oxidanidyl)methylidene]amino)-135-trimethylbenzene)-tetra-aqua-di-copper bis(bis(24-bis([carboxylato(oxidanidyl)methylidene]amino)-135-trimethylbenzene)-diaqua-dicopper) dodecahydrateExperimental 3D Coordinates
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CCDC 1478221: Experimental Crystal Structure Determination

2016

Related Article: Marta Mon, Jesús Ferrando-Soria, Thais Grancha, Francisco R. Fortea-Pérez, Jorge Gascon, Antonio Leyva-Pérez, Donatella Armentano, and Emilio Pardo|2016|J.Am.Chem.Soc.|138|7864|doi:10.1021/jacs.6b04635

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterscatena-[tris(mu-2-((2-((1-carboxylato-3-(methylsulfanyl)propyl)amino)-1-oxy-2-oxoethylidene)amino)-4-(methylsulfanyl)butanoato)-bis(mu-hydroxy)-(mu-aqua)-calcium(ii)-hexa-copper(ii) hexadecahydrate]Experimental 3D Coordinates
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CCDC 1030504: Experimental Crystal Structure Determination

2015

Related Article: Thais Grancha, Jesús Ferrando-Soria, Hong-Cai Zhou, Jorge Gascon, Beatriz Seoane, Jorge Pasán, Oscar Fabelo, Miguel Julve and Emilio Pardo|2015|Angew.Chem.,Int.Ed.|54|6521|doi:10.1002/anie.201501691

Space GroupCrystallographyCrystal Systemhexa-magnesium bis(mu-24-bis([carboxylato(oxidanidyl)methylidene]amino)-135-trimethylbenzene)-tetra-aqua-di-copper bis(bis(24-bis([carboxylato(oxidanidyl)methylidene]amino)-135-trimethylbenzene)-diaqua-dicopper) hexahydrateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1478223: Experimental Crystal Structure Determination

2016

Related Article: Marta Mon, Jesús Ferrando-Soria, Thais Grancha, Francisco R. Fortea-Pérez, Jorge Gascon, Antonio Leyva-Pérez, Donatella Armentano, and Emilio Pardo|2016|J.Am.Chem.Soc.|138|7864|doi:10.1021/jacs.6b04635

Space GroupCrystallographyCrystal SystemCrystal Structurecatena-[tris(mu-2-((2-((1-carboxylato-3-(methylsulfanyl)propyl)amino)-1-oxy-2-oxoethylidene)amino)-4-(methylsulfanyl)butanoato)-bis(mu-hydroxy)-(mu-aqua)-dichloro-calcium(ii)-hexa-copper(ii)-di-gold(i) methanol solvate trihydrate]Cell ParametersExperimental 3D Coordinates
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CCDC 1414395: Experimental Crystal Structure Determination

2016

Related Article: Marta Mon, Alejandro Pascual-Álvarez, Thais Grancha, Joan Cano, Jesús Ferrando-Soria, Francesc Lloret, Jorge Gascon, Jorge Pasán, Donatella Armentano, Emilio Pardo|2016|Chem.-Eur.J.|22|539|doi:10.1002/chem.201504176

catena-[tri-sodium (5101520-tetraphenylporphryinato)-manganese(iii) bis(tris(mu-22'-((246-trimethyl-13-phenylene)diazanylylidene)bis(oxidoacetato))-tetra-aqua-tri-copper(ii)-di-manganese(ii)) unknown solvate pentatriacontahydrate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1517224: Experimental Crystal Structure Determination

2017

Related Article: Francisco R. Fortea-Pérez, Marta Mon, Jesús Ferrando-Soria, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan Manuel Herrera, Dmitrii Osadchii, Jorge Gascon, Donatella Armentano and Emilio Pardo|2017|Nat.Mater|16|760|doi:10.1038/nmat4910

Space GroupCrystallographyCrystal SystemCrystal Structurecatena-[(mu-oxido)-hexa-ammine-di-palladium(ii) tetra-ammine-palladium(ii) bis(tris(mu-22'-((246-trimethyl-13-phenylene)diazanedi-idyl)bis(oxoacetato))-tetra-aqua-tri-copper(ii)-di-nickel(ii)) unknown solvate hydrate]Cell ParametersExperimental 3D Coordinates
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CCDC 1517225: Experimental Crystal Structure Determination

2017

Related Article: Francisco R. Fortea-Pérez, Marta Mon, Jesús Ferrando-Soria, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan Manuel Herrera, Dmitrii Osadchii, Jorge Gascon, Donatella Armentano and Emilio Pardo|2017|Nat.Mater|16|760|doi:10.1038/nmat4910

catena-[tri-sodium hemikis(di-palladium(i)-di-palladium(0)) bis(tris(mu-22'-[(246-trimethyl-13-phenylene)diazanedi-idyl]bis(oxoacetato))-tetra-aqua-tri-copper(ii)-di-nickel(ii)) unknown solvate hexapentacontahydrate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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