Search results for "spin crossover"

showing 10 items of 379 documents

Dynamics of BF 4 - anion reorientation in the spin-crossover compound [Fe(1-n-propyl-1H-tetrazole) 6 ](BF 4 ) 2 and in its Zn II analogue

1999

19 F and 11 B spin-lattice relaxation times were measured in [ Zn ( ptz ) 6 ] ( BF 4 ) 2 and in the spin-crossover compound [ Fe ( ptz ) 6 ] ( BF 4 ) 2 . For both compounds BF 4 - anion reorientation is active above 50 K. For [ Zn ( ptz ) 6 ] ( BF 4 ) 2 , the anion-reorientation dynamics is different in the temperature regions of 50-90 K, 90-120 K, and above 150 K; between 120 and 150 K it changes rapidly reflecting a structural change. In [ Fe ( ptz ) 6 ] ( BF 4 ) 2 the mechanism for the paramagnetic relaxation involving the 19 F nuclei is found to be of the diffusion-limited type according to the theory of Lowe and Tse. The present results prove that the spin-crossover takes place in a dy…

Lattice dynamicschemistry.chemical_compoundParamagnetismCrystallographyTetrafluoroborateNuclear magnetic resonancechemistrySpin crossoverSpin–lattice relaxationCrystal structure1H-tetrazoleAtomic and Molecular Physics and OpticsIonThe European Physical Journal D - Atomic, Molecular and Optical Physics
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Charge Mobility and Dynamics in Spin-Crossover Nanoparticles Studied by Time-Resolved Microwave Conductivity

2018

We use the electrode-less time-resolved microwave conductivity (TRMC) technique to characterize spin-crossover (SCO) nanoparticles. We show that TRMC is a simple and accurate mean for simultaneously as-sessing the magnetic state of SCO compounds and charge transport information on the nanometre length scale. In the low-spin state from liquid nitrogen temperature up to 360 K the TRMC measurements present two well-defined regimes in the mobility and in the half-life times, possessing similar transition tempera-tures TR near 225 K. Below TR, an activation-less regime associated with short lifetimes of the charge carri-ers points at the presence of shallow-trap states. Above TR, these states ar…

Length scaleMaterials scienceCondensed Matter - Mesoscale and Nanoscale PhysicsPhononTransition temperatureFOS: Physical sciencesThermal fluctuations02 engineering and technologyActivation energyLiquid nitrogen010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSpin crossoverChemical physicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)General Materials ScienceCharge carrierPhysical and Theoretical Chemistry0210 nano-technologyThe Journal of Physical Chemistry Letters
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Bistability in Iron(II) Spin-Crossover Systems: A Supramolecular Function

2007

Ligand field theoryBistabilityChemical physicsSpin crossoverChemistrySupramolecular chemistryNanotechnologyFunction (mathematics)
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Effect of the metal dilution on the thermal and light-induced spin transition in [FexMn1−x(bpp)2](NCSe)2: When T(LIESST) reaches T1/2

2008

International audience; The thermal and light-induced spin transition in [FexMn1−x(bpp)2](NCSe)2 (bpp = 2,6-bis(pyrazol-3-yl)pyridine) has been investigated by magnetic susceptibility, photomagnetism and diffuse reflectivity measurements. These complexes display a thermal spin transition and exhibit the light-induced excited spin state trapping (LIESST) effect at low temperature. For each mixed-crystal system, the thermal spin transition temperature, T1/2, and the relaxation temperature of the photo-induced high-spin state, T(LIESST), have been systematically determined. It appears that T1/2 decreases with the metal dilution while T(LIESST) remains unchanged, suggesting that the two interco…

Ligand field theoryCondensed matter physicsSpin states010405 organic chemistryChemistryRelaxation (NMR)Spin transition[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistryPhotomagnetismSpin crossover01 natural sciencesMagnetic susceptibilityLIESST0104 chemical sciencesCoordination chemistryInorganic ChemistrySpin crossoverMaterials ChemistryPhysical chemistryPhysical and Theoretical ChemistryMetal dilutionPhotomagnetism
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Guidelines to design new spin crossover materials

2010

International audience; This review focuses on new families of spin crossover (SCO) complexes based on polynitrile anions as new anionic ligands or on polyazamacrocycles as neutral macrocyclic ligands. We have shown that the structural and electronic characteristics (original coordination modes and high electronic delocalization) of the polynitrile anions can be tuned by slight chemical modifications such as substitution of functional groups or variation of the negative charge to design new discrete or polymeric SCO systems.In our ongoing work on the design of new molecular systems based on new ligands that can be fine-tuned via chemical modifications, another promising way which has been r…

Ligand field theoryDenticityStereochemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistryMolecular systemsIron(II) complexes010402 general chemistry01 natural sciencesInorganic ChemistryMetalMacrocyclic ligandsDelocalized electronSpin crossoverNegative chargeMagnetic propertiesMaterials Chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryChemistrySpin crossover0104 chemical sciencesCoordination polymersPolynitrileCrystallographyvisual_artvisual_art.visual_art_mediumCoordination Chemistry Reviews
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Coordination isomerism in spin crossover (SCO) materials

2021

International audience; A new series of three spin crossover (SCO) Fe(II) complexes based on a cyanocarbanion and on the neutral quinolin-8-amine (aqin) ligands, [Fe(aqin)2(tcnsme)2] (1), [Fe(aqin)2(tcnset)2] (2), and [Fe(aqin)2(tcnspr)2] (3), has been studied. The three complexes display similar molecular structures consisting of discrete [Fe(aqin)2(tcnsR)2] complexes [R = Me (1), Et (2), and Pr (3)]. Infrared spectroscopy and magnetic studies, performed on the three complexes, revealed the presence of similar SCO behaviors which strongly differ by their transition temperatures [234 K (1) < 266 K (2) < 360 K (3)]. The increase of the transition temperatures when passing from 1 to 3 may be …

Ligand field theoryMaterials scienceMolecular magnetic propertiesGeneral Physics and AstronomyInfrared spectroscopyElectron donor02 engineering and technologyCrystal structure01 natural scienceschemistry.chemical_compoundIsomerism[CHIM.ANAL]Chemical Sciences/Analytical chemistrySpin crossover0103 physical sciences[CHIM]Chemical SciencesPolymorphismInfrared spectroscopyAlkylLigand fields010302 applied physicschemistry.chemical_classificationCrystal structureTransition temperature[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyIntermolecular forcesMaterials scienceCoordination isomerismCrystallographychemistry0210 nano-technologyJournal of Applied Physics
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A thermal- and light-induced switchable one-dimensional rare loop-like spin crossover coordination polymer

2019

Rare loop-like isostructural one-dimensional coordination polymer (1D-CP) systems formulated as {Fe(DPIP)2(NCSe)2}n·4DMF (1) and {Fe(DPIP)2(NCSe)2}n·4DMF (2) were obtained by self-assembling FeII and pseudohalide NCX−(X = S, Se) ions in presence of the V-shaped bidentate bridging ligand, namely, N,N′-dipyridin-4-ylisophthalamide (DPIP), and were characterized by elemental analysis, IR spectroscopy, TGA, single crystal X-ray diffraction and powder X-ray diffraction. The magnetic studies show that complex 2 undergoes a complete thermally induced spin crossover (SCO) behavior centered at T1/2 = 120 K with ca. 5 K thermal hysteresis loop and light-induced excited spin state trapping effect (LIE…

Ligand field theoryMaterials scienceSpin states010405 organic chemistryHydrogen bondCoordination polymerBridging ligand010402 general chemistry01 natural sciencesLIESST0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundchemistrySpin crossoverIntramolecular forceDalton Transactions
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An unprecedented hetero-bimetallic three-dimensional spin crossover coordination polymer based on the tetrahedral [Hg(SeCN)4]2− building block

2019

[EN] Self-assembly of octahedral FeII ions, trans-1,2-bis(4-pyridyl) ethane (bpe) bridging ligands and [Hg(XCN)(4)](2-) (X = S (1), Se (2)) tetrahedral building blocks has afforded a new type of hetero-bimetallic Hg-II-Fe-II spin-crossover (SCO) 3D 6,4-connected coordination polymer (CP) formulated {Fe(bpe)[Hg(XCN)(4)]}(n). For X = S (1), the ligand field is close to the crossing point but 1 remains paramagnetic over all temperatures. In contrast, for X = Se (2) the complex undergoes complete thermal induced SCO behaviour centred at T-1/2 = 107.8 K and complete photoconversion of the low spin state into a metastable high-spin state (LIESST effect) with T-LIESST = 66.7 K. The current results…

Ligand field theoryMaterials scienceSpin statesCoordination polymerCrystal structureMagnetic-Properties010402 general chemistry01 natural sciencesCatalysisLIESSTParamagnetismchemistry.chemical_compoundSpin crossoverPressureMaterials ChemistrySpectroscopic investigationsPolynuclear complexesCrystal-StructureBehavior010405 organic chemistryMetals and AlloysGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyOctahedronchemistryFISICA APLICADATransitionX-RayCeramics and CompositesHg(Scn)(4)(2-) UnitStateChemical Communications
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Spin crossover in hexakis(1-(2-chloroethyl)-tetrazole)iron(II) complexes; synthesis and magnetic properties

2002

Abstract The spin-crossover complexes [Fe(teec)6](X)2 (with teec=1-(2-chloroethyl)-tetrazole and X=BF4, ClO4, PF6) possess two iron(II) sites each having a different spin-crossover behaviour. The magnetic behaviour of the complexes obtained by slow crystallisation differs strongly from those obtained by precipitation. This difference results in either a spin crossover of 50% (X=ClO4, crystalline), two gradual steps (X=BF4, PF6), or two steps, of which one is gradual and the other having a thermal hysteresis (X=ClO4 precipitated). Both 57Fe Mossbauer spectroscopy and magnetic susceptibility measurements have been recorded as a function of T. The crystal structure of [Fe(teec)6](BF4)2 has bee…

Ligand field theorySpin transitionCrystal structureMagnetic susceptibilitylaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySpin crossoverlawMössbauer spectroscopyMaterials ChemistryTetrazolePhysical and Theoretical ChemistryCrystallizationInorganica Chimica Acta
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Control of the spin state by charge and ligand substitution: two-step spin crossover behaviour in a novel neutral iron(II) complex

2014

The influence of the charge and steric hindrance on the spin state of a series of four monomeric Fe-II complexes derived from the tridentate tigands 2-(1H-benzoimidazol-2-yl)-1,10-phenanthroline (Hphenbi) and 2-(1H-benzoimidazol-2-yl-9-methyl-1,10-phenanthroline (Hmphenbi) and their deprotonated forms (phenbi(-), mphenbi(-)) are investigated. The crystal structure and magnetic properties show that [Fe(Hphenbi)(2)](BF4)(2)center dot 1.5C(6)H(5)NO(2)center dot H2O (1) and its neutral form [Fe(phenbi)(2)]center dot 2CHCl(3)center dot H2O (2) are low-spin complexes at 400 K due to the strong ligand field imparted by the terpyridine-like tigand. In contrast, the steric hindrance induced by the m…

Ligand field theorySteric effectsSpin statesChemistryStereochemistryLigandHydrostatic pressureCrystal structureInorganic ChemistrySpin crossoversCrystallographyDeprotonationSpin crossoverFISICA APLICADALigand substitutionSpin stateIron complex
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