Search results for "Paramagnetism"

showing 10 items of 354 documents

Coexistence of metamagnetism and slow relaxation of magnetization in ammonium hexafluoridorhenate.

2020

The (NH4)2[ReF6] (1) salt was studied by X-ray diffraction, Raman spectroscopy, theoretical calculations, and magnetic measurements. 1 crystallizes in the trigonal space group Pm1 (Re–F = 1.958(5) A). In the Raman spectrum of 1, splitting of the observed peaks was observed and correlated to the valence frequencies of vibration of the [ReF6]2− anion. The study of the magnetic properties of 1, through DC and AC magnetic susceptibility measurements, reveals the coexistence of metamagnetism and slow relaxation of magnetization at low temperature, which is unusual in the molecular systems based on the paramagnetic 5d metal ions reported so far.

Valence (chemistry)Materials scienceCondensed matter physicsGeneral Chemical EngineeringRelaxation (NMR)General ChemistryMagnetic susceptibilityIonMagnetizationParamagnetismsymbols.namesakesymbolsCondensed Matter::Strongly Correlated ElectronsRaman spectroscopyMetamagnetismRSC advances
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Modelling electric field control of the spin state in the mixed-valence polyoxometalate [GeV14O40]8−

2013

International audience; : The two-electron reduced mixed-valence polyoxometalate [GeV14O40](8-) presents an unusual paramagnetic behaviour as a consequence of the partial trapping of these electrons. The effect of applying an electric field is that of inducing antiferromagnetic coupling between the two delocalized electronic spins.

Valence (chemistry)SpinsSpin statesCondensed matter physicsChemistryMetals and Alloys02 engineering and technologyGeneral ChemistryElectron010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDelocalized electronParamagnetismElectric fieldPolyoxometalateMaterials ChemistryCeramics and CompositesCondensed Matter::Strongly Correlated Electrons[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyChemical Communications
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Electrically switchable magnetic molecules: inducing a magnetic coupling by means of an external electric field in a mixed-valence polyoxovanadate cl…

2015

International audience; Herein we evaluate the influence of an electric field on the coupling of two delocalized electrons in the mixed-valence polyoxometalate (POM) [GeV14 O40 ](8-) (in short V14 ) by using both a t-J model Hamiltonian and DFT calculations. In absence of an electric field the compound is paramagnetic, because the two electrons are localized on different parts of the POM. When an electric field is applied, an abrupt change of the magnetic coupling between the two delocalized electrons can be induced. Indeed, the field forces the two electrons to localize on nearest-neighbors metal centers, leading to a very strong antiferromagnetic coupling. Both theoretical approaches have…

Valence (chemistry)SpintronicsCondensed matter physicsChemistryOrganic ChemistrySpin transitionGeneral ChemistryElectronInductive couplingCatalysis[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryParamagnetismDelocalized electronNuclear magnetic resonanceElectric field
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Biferrocene Amino Acid, a Ferrocenylogoue of Ferrocene Amino Acid: Synthesis, Cross-Linking, and Redox Chemistry

2010

Access of the novel biferrocene amino acid 7 is provided by two different routes, namely, via desymmetrization of a biferrocene and via palladium-catalyzed cross-coupling of two substituted ferrocenes. The dissymmetric biferrocene 7 is head−head coupled to ureylene-bridged bis(biferrocene) 9 and also head−tail coupled to amide-bridged bis(biferrocene) 14. The monomer 7 and the dimers 9 and 14 are oxidized to mixed-valent cations 7+, 9+, 92+, and 142+. The valencies are trapped in the solid state as shown by Mossbauer and EPR spectroscopy and by X-ray diffraction analysis of [7](I3). Paramagnetic NMR shift studies (7 → 7+) suggest that the hole is localized at the N-substituted ferrocene uni…

Valence (chemistry)StereochemistryOrganic ChemistryDesymmetrizationRedoxlaw.inventionInorganic Chemistrychemistry.chemical_compoundParamagnetismCrystallographyMonomerchemistryFerrocenelawMössbauer spectroscopyPhysical and Theoretical ChemistryElectron paramagnetic resonanceOrganometallics
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Iso-valence Co(II) and mixed-valence Co(II/III) tetranuclear complexes: Synthesis, structure, magnetic properties and DFT study

2013

Abstract The reaction of Co(ClO4)2·6H2O with symmetrical N4O3 coordinating heptadentate ligand (H3L) in presence of triethylamine yielded cobalt(II) tetranuclear complexes [Co4(L)2](ClO4)2, 1. When the same reaction is carried out with sodium azide instead of triethylamine afforded tetranuclear mixed-valence Co(II/III) species, [Co4(L)2(μ1,3–N3)2](ClO4)2, 2. Here L3− is the deprotonated form of 2,6-bis[{{(1-hydroxy-2-methylpropan-2-yl)(pyridine-2-ylmethyl)}amino}methyl]-4-methylphenol. Complex 1 crystallizes in the cubic system, space group Fd-3c, with unit-cell parameters a = b = c = 43.320(5) A, Z = 48, whereas complex 2 crystallizes in the space group I41/a in the tetragonal crystal syst…

Valence (chemistry)Stereochemistrychemistry.chemical_elementCrystal structureInorganic Chemistrychemistry.chemical_compoundTetragonal crystal systemParamagnetismCrystallographyDeprotonationchemistryMaterials ChemistryDensity functional theoryPhysical and Theoretical ChemistryTriethylamineCobaltPolyhedron
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Magnetic Control over the Fractal Dimension of Supramolecular Rod Networks

2021

<p>Controlling supramolecular polymerization is of fundamental importance to create advanced materials and devices. Here we show that the thermodynamic equilibrium of Gd<sup>3+</sup>-bearing supramolecular rod networks is shifted reversibly at room temperature in a static magnetic field of up to 2 T. Our approach opens opportunities to control the structure formation of other supramolecular or coordination polymers that contain paramagnetic ions.</p>

[PHYS]Physics [physics]chemistry.chemical_classificationMagnetic energy010405 organic chemistryChemistryThermodynamic equilibriumSupramolecular chemistryAucunGeneral ChemistryPolymer010402 general chemistryMagnetostatics01 natural sciencesBiochemistryCatalysis0104 chemical sciencesParamagnetismColloid and Surface ChemistryPolymerizationChemical physicsSelf-assemblyComputingMilieux_MISCELLANEOUS
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Cubane-Type Mo3CoS4 Molecular Clusters with Three Different Metal Electron Populations: Structure, Reactivity and Their Use in the Synthesis of Hybri…

2004

Heterodimetallic cubane-type complexes coordinated to diphosphanes [Mo(3)CoS(4)(dmpe)(3)Cl(4)](+) ([1](+)) (dmpe=1,2-bis(dimethylphosphanyl)ethane), [Mo(3)CoS(4)(dmpe)(3)Cl(4)] (1) and [Mo(3)CoS(4)(dmpe)(3)Cl(3)(CO)] (2) with 14, 15 and 16 metal electrons, respectively, have been prepared from the [Mo(3)S(4)(dmpe)(3)Cl(3)](+) trinuclear precursor using [Co(2)(CO)(8)] or CoCl(2) as cobalt source. Cluster complexes [1](+) and 1 are easily interconverted chemically and electrochemically. The Co-Cl distance increases upon electron addition and substitution of the chlorine atom coordinated to cobalt with CO only takes place in presence of a reducing agent to give complex 2. Structural changes in…

biologyChemistryOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryZero field splittingMagnetic susceptibilityCatalysisParamagnetismchemistry.chemical_compoundCrystallographyUnpaired electronCubanebiology.proteinAntiferromagnetismCobaltOrganic anionChemistry - A European Journal
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Iron oxide superparamagnetic nanocarriers bearing amphiphilic N-heterocyclic choline analogues as potential antimicrobial agents

2015

Magnetic nanoparticles represent an advanced tool in biomedicine because they can be simultaneously functionalized and guided using a magnetic field. Iron oxide magnetic nanoparticles precoated with oleic acid and bearing novel antimicrobial N-heterocyclic choline analogues, namely O-, N- and O,N-bis-undecyl-substituted N-(2-hydroxyethyl)-1,2,3,4-tetrahydroisoquinolinium derivatives, have been obtained as potential biomedical agents for drug delivery and antimicrobial therapy. Structural and size determinations for the novel synthesized magnetic nanosystems were carried out based upon magnetogranulometry, dynamic light-scattering measurements and X-ray diffraction analysis. The most expecte…

biologyChemistryfungiBacillus cereusNanoparticleGeneral Chemistryequipment and suppliesbiology.organism_classificationAntimicrobialCombinatorial chemistryInorganic ChemistryBiochemistryDrug deliveryAmphiphileMagnetic nanoparticlesNanocarriershuman activitiesSuperparamagnetismApplied Organometallic Chemistry
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Binding Profiles of Self-Assembled Supramolecular Cages from ESI-MS Based Methodology

2018

Confined molecular environments have peculiar characteristics that make their properties unique in the field of biological and chemical sciences. In recent years, advances in supramolecular capsule and cage synthesis have presented the possibility to interpret the principles behind their self‐assembly and functions, which has led to new molecular systems that display outstanding properties in molecular recognition and catalysis. Herein, we report a rapid method based on ESI‐MS to determine the binding profiles for linear saturated dicarboxylic acids in a series of different cages. The cages were obtained by self‐assembly of modified tris(pyridylmethyl)amine (TPMA) complexes and diamines cho…

cage compounds; dynamic covalent chemistry; molecular recognition; supramolecular chemistry; tris(pyridylmethyl)amine; Chemistry (all)Electrospray ionizationSupramolecular chemistry010402 general chemistry01 natural sciencesCatalysissupramolecular chemistryParamagnetismMolecular recognitionComputational chemistrysupramolekulaarinen kemiaSettore CHIM/01 - Chimica AnaliticaSpectroscopyta116010405 organic chemistryChemistryOrganic ChemistryChemistry (all)Dynamic covalent chemistrySettore CHIM/06 - Chimica OrganicaGeneral Chemistry0104 chemical sciencesProton NMRtris(pyridylmethyl)amineAmine gas treatingdynamic covalent chemistrymolecular recognitioncage compounds
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Coordination chemistry of N,N′-bis(coordinating group substituted)oxamides: a rational design of nuclearity tailored polynuclear complexes

1999

Abstract The coordinating properties of N , N ′-bis(coordinating group substituted)oxamides have been thoroughly investigated both in aqueous solution and in the solid state. The easy cis – trans isomerization equilibria that they exhibit together with the great variety of N , N ′-substituents which can be used to play on the overall charge, complexing ability and polarity, make them very suitable ligands in designing homo- and heterometallic species. The knowledge of their complex formation in aqueous solution by potentiometry and using the hydrogen ion concentration as a probe, allowed us to settle the basis of a rational design of oxamidate-containing polynuclear species whose nuclearity…

chemistry.chemical_classificationAqueous solutionChemistryStereochemistryRational designCoordination complexInorganic ChemistryParamagnetismDeprotonationComputational chemistryGroup (periodic table)Materials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryIsomerizationCoordination Chemistry Reviews
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