Search results for "cobalt."

showing 10 items of 969 documents

Compensation of steric demand by cation–π interactions, cobaltocenium cations as guests in tetraurea calix[4]arene dimers

2003

The affinities of ferrocene (2) and the cobaltocenium cation (3+), which have roughly the same size and differ in their charge, towards the inner cavity of the dimeric capsule formed by tetraurea calix[4]arene (1) were studied in C2D4Cl2 solutions. While 3+, which occupies more than 75% of the internal volume of the dimer, is readily encapsulated this is not the case for 2. This is probably due to cation-pi interactions, which operate only between 3+ and the aromatic rings of the calix[4]arene dimer. We found that the affinity of the cobaltocenium cation is higher than that of the tropylium cation (4+) and is only 2-3 times less than that of the tetraethylammoniun cation (5+). From the vari…

Steric effectsMagnetic Resonance SpectroscopyMetallocenesTropylium cationStereochemistryDimerBiochemistryDiffusionchemistry.chemical_compoundPhenolsCationsCalixareneOrganometallic CompoundsUreaFerrous CompoundsPhysical and Theoretical ChemistryBenzeneOrganic ChemistryTetraethylammoniumHydrogen BondingAromaticityCobaltCrystallographychemistryFerroceneProton NMRCalixarenesDimerizationOrg. Biomol. Chem.
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Planar-Chiral 1,1 '-Diboryl Metallocenes: Diastereoselective Synthesis from Boryl Cyclopentadienides and Spin Density Analysis of a Diborylcobaltocene

2017

International audience; The reaction of nonsubstituted alkali metal cyclopentadienides with haloboranes leads to similar to 90:10 mixtures of isomeric diene products that can be deprotonated to give simple boryl cyclopentadienides. We extended this transformation to the sterically hindered lithium tert-butylcyclopentadienide 1 using FBMe(s)2 (Mes = 2,4,6-trimethylphenyl) and ClBCy2 as electrophiles. The boryl group is selectively introduced in the remote position to minimize steric congestion. The new boryl dienes are obtained as mixtures of isomers, and subsequent deprotonation with MeLi or LiHMDS affords the lithium 1,3-disubstituted cyclopentadienides Sa,b in yields over 95%. Direct asse…

Steric effectselectronDienechemistry.chemical_elementanion recognition[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryPhotochemistryligand01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundDeprotonationredox chemistryCobaltocenePhysical and Theoretical ChemistryConformational isomerismbidentate lewis-acids010405 organic chemistryChemistryDiastereomercrystal-structure[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry0104 chemical sciencessubstituted ferrocenesElectrophileLithiumactivationolefin polymerizationboron
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CCDC 989261: Experimental Crystal Structure Determination

2014

Related Article: Maria-Gabriela Alexandru, Diana Visinescu, Nadia Marino, Giovanni De Munno, Julia Vallejo, Francesc Lloret, Miguel Julve|2014|Eur.J.Inorg.Chem.||4564|doi:10.1002/ejic.201402190

Tetraphenylphosphonium tricyano-(29-dimethyl-110-phenanthroline)-cobalt(ii) trihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Magnetic properties of Co–Al, Ni–Al, and Mg–Al hydrotalcites and the oxides formed upon their thermal decomposition

2002

The magnetic behaviour of Co–Al, Ni–Al, and Mg–Al hydrotalcites (HTlc) with a M2+/Al3+ molar ratio of 3 and carbonates in the interlayer, as well as the mixed oxides obtained after calcination at 823 K for 5 h, has been investigated by DC and AC magnetic susceptibility measurements and isothermal magnetisation. The samples were also characterised by ICP-OES and XRD. The magnetic measurements show that Co–Al and Ni–Al HTlcs behave as ferromagnets, with ordering temperatures of approximately 6–7 K in both cases, and displaying hysteresis loops at 2 K with coercive fields of 4.2 and 5.5 mT, respectively, whereas the Mg–Al-HTlc shows the expected diamagnetic behaviour. A solid solution of cobal…

Thermal decompositionAnalytical chemistrychemistry.chemical_elementGeneral ChemistryMagnetic susceptibilitylaw.inventionMagnetizationNuclear magnetic resonanceFerromagnetismchemistrylawMaterials ChemistryDiamagnetismCalcinationCobaltSolid solutionJ. Mater. Chem.
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Ionic liquid-cobalt complexes: a thermochromic interaction

Thermochromism Ionic Liquids Cobalt complexesSettore CHIM/06 - Chimica Organica
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Reversible solvatomagnetic switching in a single-ion magnet from an entatic state

2016

We have developed a new strategy for the design and synthesis of multifunctional molecular materials showing reversible magnetic and optical switching.

Thermochromismgenetic structuresSingle ion010405 organic chemistryChemistrychemistry.chemical_elementEntatic stateNanotechnologyGeneral Chemistryequipment and supplies010402 general chemistry01 natural scienceseye diseases0104 chemical sciencesChemistryTransition metalMagnetMagnetic relaxationhuman activitiesCobaltQuantum computerChemical Science
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Ionic Liquids-Cobalt (II) Thermochromic Complexes: How the Structure Tunability Affects "Self-contained" Systems

2021

With the aim of obtaining thermochromic systems with potential applications in solar energy storage, we evaluated the behavior of some sugar-based ionic liquids (ILs)–Co(NTf₂)₂ complexes, in IL solution, as a function of temperature. Different structural changes on the cation, the nature of the anion, and the nature of the IL used as the solvent were considered. The analysis of the above factors was carried out through a combined approach of different techniques, that is, variable temperature UV–vis and NMR spectroscopies, conductivity, and thermal gravimetric analysis. The thermochromic systems were analyzed both as solutions and as thin films, and the data collected highlight the defining…

Thermogravimetric analysisMaterials scienceGeneral Chemical Engineeringchemistry.chemical_element02 engineering and technologyConductivity010402 general chemistry01 natural scienceschemistry.chemical_compoundEnvironmental ChemistryThin filmThermochromismRenewable Energy Sustainability and the EnvironmentGeneral ChemistrySettore CHIM/06 - Chimica OrganicaAtmospheric temperature range021001 nanoscience & nanotechnology0104 chemical sciencesSolventchemistryChemical engineeringIonic liquidIonic liquids Thermochromism0210 nano-technologyCobaltthermochromism ionic liquids polymer films switchable magnetism
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Reaction of thiophene with mono- and bimetallic Ni–Co particles supported on γ-Al2O3 and HDS activities of obtained sulfides

2009

Abstract Reaction between thiophene and M/γ-Al2O3 (20 wt.%, M = Ni, Co, 2Ni–Co and 2Co–Ni) was studied by thermal gravimetric analysis (TGA) and by sulfidation in a fixed bed microreactor. The samples were prepared by incipient wetness impregnation followed by drying and reduction in hydrogen flow at 450 °C. Formation of bimetallic particles in samples containing both Ni and Co was confirmed by HRTEM with EDX analysis. The reaction with thiophene (20 or 40 mbar) was done at 360 °C in hydrogen atmosphere. TGA of the reaction with thiophene revealed that the initial rate of sulfidation drops sharply when going from Ni/γ-Al2O3 to Co/γ-Al2O3 (by a factor of 40 under used conditions). It follows…

Thermogravimetric analysisProcess Chemistry and TechnologyInorganic chemistrySulfidationchemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistry13. Climate actionThiophene0210 nano-technologyBimetallic stripHydrodesulfurizationCobaltIncipient wetness impregnationApplied Catalysis A: General
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Electrosynthesis of Sn-Co nanowires in alumina membranes

2010

A fabrication process of amorphous nanowires of Sn-Co alloys, based on electrodeposition into anodic alumina membranes, is described. It is shown that nanowires of tin-cobalt alloys with different compositions can be produced by varying electrodeposition time and concentration ratio of salts dissolved into the electrolytic bath. Importance of the chelating agent to produce amorphous Sn-Co alloys has also been addressed. Electrodepositions were carried out potentiostatically at -1 V versus Saturated Calomel Electrode and 60 degrees C for times ranging from 10 to 90 minutes; the atomic fraction of Co2+ in the aqueous electrolyte (Co2+/(Co2+ + Sn2+)) was varied from 0.33 to 0.67. Nanowires asp…

Tin–Cobalt Alloys Template Synthesis Alumina Membranes Li-Ion Batteries Tin AnodeMaterials scienceScanning electron microscopeAlloytechnology industry and agricultureBiomedical EngineeringNanowireAnalytical chemistryEnergy-dispersive X-ray spectroscopyBioengineeringGeneral ChemistryElectrolyteengineering.materialequipment and suppliesCondensed Matter PhysicsConcentration ratioAmorphous solidSettore ING-IND/23 - Chimica Fisica ApplicataSaturated calomel electrodeengineeringGeneral Materials Science
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Oral intake of cadmium, cobalt, copper, iron, lead, nickel, manganese and zinc in the university student's diet.

1993

A duplicate diet meal study was carried out with a group of university students living in a hostel, in order to estimate the intake of Zn, Cd, Co, Cu, Fe, Mn, Ni and Pb. Zn, Cu, Fe, Mn and Ni were determined by flame atomic absorption spectrophotometry and Cd, Co and Pb by graphite furnace atomic absorption spectrophotometry after a nitric acid wet digestion procedure. The estimated intake values from the contents of breakfast, lunch, dinner and drinks were compared with the values of the Provisional Tolerable Daily Intake (PTDI) in the case of Cd and Pb, Recommended Dietary Allowances (RDA) of Co, Fe and Zn and Estimated Safe and Adequate Dietetic Daily Intake (ESADDI) of Cu and Mn. Neithe…

Tolerable daily intakeMealCadmiumUniversitiesSpectrophotometry AtomicMetallurgychemistry.chemical_elementNutritional StatusFood ContaminationZincManganeselaw.inventionDietTrace ElementschemistrylawSpainHumansAtomic absorption spectroscopyGraphite furnace atomic absorptionStudentsCobaltFood AnalysisFood ScienceNuclear chemistryDie Nahrung
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