Search results for "Metals"

showing 10 items of 2013 documents

Isomorphous replacement of MII ions in MII–GdIII dimers (MII = CuII, MnII, NiII, CoII, ZnII): magnetic studies of the products

2011

Complexes [M(II)Gd(III){pyCO(OEt)pyC(OH)(OEt)py}₃](ClO₄)₂·EtOH [M(II) = Cu(II) (1), Mn(II) (2), Ni(II) (3), Co(II) (4) and Zn(II) (5)] crystallize in the monoclinic Cc space group and contain one hexacoordinate M(II) ion and one enneacoordinate Gd(III) ion, bridged by three {pyCO(OEt)pyC(OH)(OEt)py}⁻ ligands. Magnetic susceptibility measurements indicate a ferromagnetic interaction for 1 and antiferromagnetic interactions for 2-4. Using the Ĥ = -JŜ(Gd(III))Ŝ(M(II)) spin Hamiltonian formalism, fits to the magnetic susceptibility data yielded J values of +0.32 cm⁻¹ for 1, -1.7 cm⁻¹ for 2, and -0.22 cm⁻¹ for 3. In complex 4, the orbital contributions of Co(II) precluded the determination of th…

ManganeseChemistryStereochemistryMolecular ConformationHexacoordinateSpin hamiltonianGadoliniumCobaltCrystallography X-RayMagnetic susceptibilityInductive couplingIonInorganic ChemistryMagneticsZincCrystallographyFerromagnetismCoordination ComplexesMetalsNickelAntiferromagnetismDimerizationCopperMonoclinic crystal systemDalton Transactions
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Manganese(iv) oxamato-catalyzed oxidation of secondary alcohols to ketones by dioxygen and pivalaldehyde

1998

A new manganese(IV) oxamato complex possessing a bis(moxo) dimanganese core has been synthesized, magnetically and structurally characterized, and found to catalyze the aerobic oxidation of secondary alcohols to ketones with cooxidation of pivalaldehyde to pivalic acid with good yields and high selectivities. Ruiz Garcia, Rafael, Rafael.Ruiz@uv.es ; Fernandez Picot, Isabel, Isabel.Fernandez@uv.es ; Pedro Llinares, Jose Ramon, Jose.R.Pedro@uv.es ; Rosello Arce, Antonio Luis, Antonio.L.Rosello@uv.es ; Castro Bleda, Isabel, Isabel.Castro@uv.es

ManganesePivalic acidDioxygenUNESCO::QUÍMICA::Química inorgánicaUNESCO::QUÍMICAMetals and Alloyschemistry.chemical_elementGeneral ChemistryManganeseKetones:QUÍMICA::Química inorgánica [UNESCO]:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundchemistryAlcoholsOxidationMaterials ChemistryCeramics and CompositesOxidation of secondary alcohols to ketonesOrganic chemistryManganese ; Oxidation ; Alcohols ; Ketones ; Dioxygen
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Sunscreen Products as Emerging Pollutants to Coastal Waters

2013

A growing awareness of the risks associated with skin exposure to ultraviolet (UV) radiation over the past decades has led to increased use of sunscreen cosmetic products leading the introduction of new chemical compounds in the marine environment. Although coastal tourism and recreation are the largest and most rapidly growing activities in the world, the evaluation of sunscreen as source of chemicals to the coastal marine system has not been addressed. Concentrations of chemical UV filters included in the formulation of sunscreens, such as benzophehone 3 (BZ-3), 4-methylbenzylidene camphor (4-MBC), TiO2 and ZnO, are detected in nearshore waters with variable concentrations along the day a…

Marine ChemistryMarine and Aquatic Scienceslcsh:MedicineHeavy MetalsOceanographyWater ChemistryAnalytical Chemistryvisual_art.visual_artistWater AnalysisWater QualityMicroalgaeWater pollutionlcsh:ScienceTitaniumMultidisciplinarySunbathingEcologyChemistryEcologyChemical OceanographyMarine EcologyChemical oceanographyZincChemistryEnvironmental chemistryvisual_artCoastal EcologyResearch ArticlePollutantsAlgal bloomPhosphatesBenzophenonesInhibitory Concentration 50Chemical AnalysisSunbathingMediterranean SeaHumansEnvironmental ChemistrySeawaterMarine ecosystemBiological oceanographyBiologyDiatomsPollutantBiological Oceanographylcsh:RKineticsSpainEarth SciencesSeawaterlcsh:QSunscreening AgentsWater Pollutants ChemicalEnvironmental Protection
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A lap joint simulant laboratory test method of aluminium alloys

2015

A lap joint simulant cavity (LJSC) with a gap thickness of 200 μm has been developed to test corrosion of assembled coated aluminium alloys. The LJSC was instrumented with electrodes allowing simultaneous pH and potential measurements in 0.5 M NaCl solution. Assuming the outer part of the LJSC is electrochemically inactive (painted sheet) it was confirmed that in free corroding conditions the pH inside the LJSC tends more towards alkalinisation. On the opposite, if the outer part of the LJSC is electrochemically active (unpainted sheet) the pH inside the LJSC tends towards an acidic value.

Mass transportMaterials scienceMechanical EngineeringMetallurgyMetals and AlloysLaboratory Test Methodchemistry.chemical_elementGeneral MedicineSurfaces Coatings and FilmsCorrosionLap jointchemistryMechanics of MaterialsAluminiumElectrodeMaterials ChemistryEnvironmental ChemistryComposite materialMaterials and Corrosion
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Metal–organic frameworks as chemical nanoreactors for the preparation of catalytically active metal compounds

2023

Since the emergence of metal-organic frameworks (MOFs), a myriad of thrilling properties and applications, in a wide range of fields, have been reported for these materials, which mainly arise from their porous nature and rich host-guest chemistry. However, other important features of MOFs that offer great potential rewards have been only barely explored. For instance, despite the fact that MOFs are suitable candidates to be used as chemical nanoreactors for the preparation, stabilization and characterization of unique functional species, that would be hardly accessible outside the functional constrained space offered by MOF channels, only very few examples have been reported so far. In par…

Materials ChemistryMetals and AlloysCeramics and CompositesGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical Communications
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Bis[cyclic (alkyl)(amino)carbene] isomers: Stable trans -bis(CAAC) versus facile olefin formation for cis -bis(CAAC)

2022

A trans-bis(CAAC) was isolated and shown to be a ditopic ligand for rhodium and iridium. The cis-isomer is unstable towards intramolecular CC-bond formation, however, its formal insertion products into the bonds of H2O and NH3 were identified.

Materials ChemistryMetals and AlloysCeramics and CompositesGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical Communications
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pH Feedback Systems to Program Autonomous Self-Assembly and Material Lifecycles

2022

pH-responsive systems have gained importance for the development of smart materials and for biomedical applications because they can switch between different states by simple acid/base triggers. However, such equilibrium systems lack the autonomous behavior that is so ubiquitous in living systems that self-regulate out of equilibrium. As a contribution to the emerging field of autonomous chemical systems, we have developed pH feedback systems (pH-FS) based on the coupling of acid- and base-producing steps in chemical reaction networks. The resulting autonomous nonlinear pH curves can be coupled with a variety of pH-sensitive building blocks to program the life cycles of the associated trans…

Materials ChemistryMetals and AlloysCeramics and CompositesGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials
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Epoxidation vs. dehydrogenation of allylic alcohols: heterogenization of the VO(acac)2 catalyst in a metal–organic framework

2022

Allylic alcohol epoxidation and dehydrogenation reactivity is distinguished when VO(acac)2 is used in solution or anchored in a metal–organic framework (MOF). The chemical mechanism depends on the electronic profile of alkene substituents when the vanadyl complex is used in the homogenous phase. However, confinement effects imparted by MOF channels allow gaining control of the chemoselectivity toward the dehydrogenation product.

Materials ChemistryMetals and AlloysCeramics and CompositesGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical Communications
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Chiral carbonyl hypoiodites

2023

Three chiral carbonyl hypoiodites, R–C(O)OI, have been prepared from N-protected (S)-valine to give the ligand-stabilised (S)-valinoyl hypoiodite complexes with 4-dimethylaminopyridine, 4-pyrrolidinopyridine, and 4-morpholinopyridine as the stabilising ligands. The identity of the complexes was established by NMR (1H, 13C, 1H–15N HMBC) and single crystal X-ray diffraction analysis. peerReviewed

Materials ChemistryMetals and AlloysCeramics and CompositesGeneral ChemistryCatalysiskarbonyylitSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials
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Chemistry of two-dimensional pnictogens: emerging post-graphene materials for advanced applications

2023

The layered allotropes of group 15 (P, As, Sb and Bi), also called two-dimensional (2D) pnictogens, have emerged as one of the most promising families of post-graphene 2D-materials. This is mainly due to the great variety of properties they exhibit, including layer-dependent bandgap, high charge-carrier mobility and current on/off ratios, strong spin-orbit coupling, wide allotropic diversity and pronounced chemical reactivity. These are key ingredients for exciting applications in (opto)electronics, heterogeneous catalysis, nanomedicine or energy storage and conversion, to name a few. However, there are still many challenges to overcome in order to fully understand their properties and brin…

Materials ChemistryMetals and AlloysCeramics and CompositesGeneral ChemistryMaterialsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical Communications
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