Search results for "Propietats magnètiques"

showing 7 items of 7 documents

Special Issue 'Spin Crossover (SCO) Research'

2016

This special issue, entitled “Spin Crossover (SCO) Research”, illustrates the current relevance of a focused topic, which is inturn highly versatile. Indeed, the collection of papers presented constitutes a sampler that shows the topical importance of this area by attracting the interest of many top researchers and how it is approached under a multidisciplinary perspective.[...]

Computer sciencePropietats magnètiquesMagnetoquímicaNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyLigands01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsLligandsChemistry (miscellaneous)Multidisciplinary approachSpin crossoverMagnetic propertiesMaterials ChemistryRelevance (information retrieval)Engineering ethics0210 nano-technologyMagnetochemistry
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Antiferromagnetic Interactions in Copper(II) µ-Oxalato Dinuclear Complexes: The Role of the Counterion

2018

We report the preparation, crystal structure determination, magnetic properties and DFT calculations of five oxalato-bridged dicopper(II) complexes of formula [Cu-2(bpy)(2-)(H2O)(2)(C2O4)](CF3SO3)(2) (1), [Cu-2(bpy)(2)(C2O4)](PF6)(2) (2), [Cu-2(bpy)(2)(C2O4)](ClO4)(2) (3), [Cu-2(bpy)(2)Cl-2(C2O4)]center dot H2O (4) and [Cu-2(bpy)(2)(NO2)(2)(C2O4)] (5) (bpy = 2,2'-bipyridine and C2O42-= oxalate). Compounds 1, 2, 4 and 5 crystallize in the monoclinic system and 3 crystallizes in the triclinic system. The oxalate ligands in 1-5 adopt the bis-bidentate coordination mode and the two bpy molecules act as terminal ligands. The coordination of the counterions and the surroundings of the copper(II) …

Dinuclear complexesMatériauxFerromagnetismechemistry.chemical_elementCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistryTriclinic crystal system010402 general chemistry01 natural sciencesOxalateInorganic Chemistrychemistry.chemical_compoundOxalatoMagnetic propertiesAntiferromagnetismMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryGénie des procédéschemistry.chemical_classificationCoure010405 organic chemistryPropietats magnètiquesCopper0104 chemical sciences3. Good healthCrystallographyDensity functional calculationschemistryFerromagnetismCounterionCopperMonoclinic crystal system
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Structural and magnetic studies of mononuclear lanthanide complexes derived from Ν-rich chiral Schiff bases.

2021

Zn(II) complexes containing N, N,N and N,N,N pyridine (dPy) ligands tend to display improved fluorescence efficiencies in comparison with their starting ligands benefiting from the chelation enhanced effect (CHEF) and preventing photoinduced electron transfer (PET) mechanisms by the coordination of their lone pair electrons. Nevertheless, the size of Zn(II) makes steric crowding an important factor to be considered, since it can promote the elongation of the coordination bonds that weakens their strength and favors the reduction of fluorescence efficiencies through PET processes. For that reason, in this contribution we have performed a systematic study of Zn(II) compounds based on α-acetam…

Inorganic ChemistryLanthanideMagnetizationCrystallographyMaterials sciencePropietats magnètiquesQuiralitatMagnetic propertiesRelaxation (physics)ChiralitySingle crystalPowder diffraction
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Chiral Oxazolidine Complexes Derived from Phenolic Schiff Bases

2020

Schiff bases derived from pyridyl- or salicyl-aldehydes and aminoalcohols can evolve to heterocyclic oxazolidines, which in the presence of cations allow the formation of uncommon coordination compounds. In this work, we report new NiII and mixed valence MnII/ MnIV complexes derived from pyridyl oxazolidines and the unprecedented characterization of enantiomerically pure oxazolidines derived from the condensation of o-vanillin with phenylglycinol in the presence of NiII cations. The different reactivity of the pyridinic or phenolic Schiff bases has been compared, and the new systems have been structurally, optically, and magnetically characterized.

OxazolidinePropietats magnètiques010405 organic chemistryLigands (Biochemistry)Lligands (Bioquímica)General Chemistry010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryAlcoholsMagnetic propertiesPolymer chemistryGeneral Materials ScienceCrystal Growth & Design
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Giant barocaloric effects over a wide temperature range in superionic conductor AgI

2017

Current interest in barocaloric effects has been stimulated by the discovery that these pressure-driven thermal changes can be giant near ferroic phase transitions in materials that display magnetic or electrical order. Here we demonstrate giant inverse barocaloric effects in the solid electrolyte AgI, near its superionic phase transition at ~420 K. Over a wide range of temperatures, hydrostatic pressure changes of 2.5 kbar yield large and reversible barocaloric effects, resulting in large values of refrigerant capacity. Moreover, the peak values of isothermal entropy change (60 J K−1 kg−1 or 0.34 J K−1 cm−3) and adiabatic temperature changes (18 K), which we identify for a starting tempera…

Phase transitionMaterials scienceThermal propertiesScienceHydrostatic pressureGeneral Physics and Astronomy02 engineering and technologyElectrolytePropietats tèrmiques7. Clean energy01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyIsothermal processArticle0103 physical sciencesThermalMagnetic propertiesFast ion conductorlcsh:Science010306 general physicsAdiabatic processMultidisciplinaryCondensed matter physicsPropietats magnètiquesQGeneral ChemistryAtmospheric temperature rangeCiència dels materials021001 nanoscience & nanotechnologyMaterials science0403 Geologylcsh:Q0210 nano-technologyNature Communications
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Pulsed-field studies of the magnetization reversal in molecular nanomagnets

2004

We report experimental studies of crystals of Mn12 molecular magnetic clusters in pulsed magnetic fields with sweep rates up to 4x10^3 T/s. The steps in the magnetization curve are observed at fields that are shifted with respect to the resonant field values. The shift systematically increases as the rate of the field sweep goes up. These data are consistent with the theory of the collective dipolar relaxation in molecular magnets.

PhysicsCondensed matter physicsField (physics)Molecular magnetsPropietats magnètiquesEnergy level splittingMagnetization reversalFOS: Physical sciences02 engineering and technologyNanostructured materials021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesElectronic Optical and Magnetic MaterialsMagnetic fieldCondensed Matter - Other Condensed MatterTunnel effectMagnet0103 physical sciencesMagnetic propertiesMaterials nanoestructurats010306 general physics0210 nano-technologySingle crystalOther Condensed Matter (cond-mat.other)
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From Bowls to Capsules: Assembly of Hexanuclear Ni II Rings Tailored by Alkali Cations

2020

An anionic hexanuclear NiII metallamacrocycle with endo and exo linking sites has been employed as a building block to generate a series of capsules and bowls of nanometric size. The supramolecular arrangement of the {Ni6 } rings was tailored by the size of the alkali cations, showing the transition from {Ni6 -M2 -Ni6 } capsules (M=LiI and NaI ) to {Ni6 -M} bowls (M=KI and CsI ). The alkyl co-cations are determinant to stabilize the assemblies by means of CH⋅⋅⋅π interactions on the exo side of the metallamacrocycles. The effect on the topology of the supramolecular assemblies of the cation size, cation charge, Et3 NH+ or Me4 N+ counter cations has been analyzed. Magnetic measurements reveal…

chemistry.chemical_classificationNíquelPropietats magnètiques010405 organic chemistryOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryBlock (periodic table)Alkali metal01 natural sciencesCatalysisAnàlisi de conglomerats0104 chemical sciencesCrystallographyNickelCluster analysischemistryNickelMagnetic propertiesAntiferromagnetismSelf-assemblyGround stateAlkylChemistry – A European Journal
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