Search results for "antiferromagnetic"

showing 10 items of 39 documents

One-dimensional oxalato-bridged copper(II) complex possessing two structurally different metallic centres

2001

Abstract The crystal structure of the oxalato-bridged copper(II) compound [Cu2(μ-ox)2(ampy)3]n 1 (ox=oxalate dianion, ampy=2-amino-3-methylpyridine) consists of infinite corrugated one-dimensional chains in which two types of copper(II) centres, five- and six-coordinated, are bridged sequentially by asymmetric bis-bidentate oxalato ligands. Magnetic susceptibility measurements show the occurrence of a significant intrachain antiferromagnetic coupling (J=−22.9 cm −1 ) .

Copper complexChemistryInorganic chemistrychemistry.chemical_elementCrystal structureCopperMagnetic susceptibilityOxalateAntiferromagnetic couplingInorganic ChemistryMetalCrystallographychemistry.chemical_compoundvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryInorganic Chemistry Communications
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Coexistence of spin-crossover and antiferromagnetic coupling phenomena in the novel dinuclear Fe(II) complex [Fe(dpa)(NCS)2]2bpym

2003

Abstract The iron(II) spin crossover dinuclear compound [Fe(dpa)(NCS) 2 ] 2 bpym where dpa = 2,2 ′ -dipyridylamine and bpym = 2,2 ′ -bipyrimidine has been synthesized and characterized. Variable-temperature magnetic susceptibility and 57 Fe Mossbauer spectroscopy data provide evidence for a rather complete and continuous S=2 ( HS )↔S=0 (LS) spin-crossover behavior taking place in the temperature range 400–50 K (T 1/2 =245 K ) without the presence of a plateau at 50% of conversion. The absence of such plateau, which is characteristic of all dinuclear compounds so far studied, is interpreted in terms of synergetic effect between intramolecular and intermolecular interactions.

CrystallographyNuclear magnetic resonanceChemistrySpin crossoverIntramolecular forceMössbauer spectroscopyIntermolecular forceGeneral Physics and AstronomyPhysical and Theoretical ChemistryAtmospheric temperature rangePlateau (mathematics)Magnetic susceptibilityAntiferromagnetic couplingChemical Physics Letters
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Interplay of Antiferromagnetic Coupling and Spin Crossover in Dinuclear Iron(II) Complexes

2003

This article reports on the study of the interplay between magnetic coupling and spin transition in 2,2′-bipyrimidine (bpym)-bridged iron(II) dinuclear compounds. Coexistence of both phenomena has been observed in [Fe(bpym)(NCS)2]2bpym, [Fe(bpym)(NCSe)2]2bpym and [Fe(bt)(NCS)2]2bpym (bpym = 2,2′-bipyrimidine, bt = 2,2′-bithiazoline) by the action of external physical factors namely pressure or electromagnetic radiation. Competition between magnetic exchange and spin crossover has been studied in [Fe(bpym)(NCS)2]2bpym at 6.3 kbar. LIESST experiments carried out in [Fe(bpym)(NCSe)2]2bpym and [Fe(bt)(NCS)2]2bpym at 4.2 K have shown that is possible to achieve dinuclear molecules with different…

CrystallographySpin statesCondensed matter physicsChemistrySpin crossoverSpin transitionMoleculeInductive couplingLIESSTAntiferromagnetic couplingMagnetic exchange
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Cyanide-bridged Fe(III)–Co(II) bis double zigzag chains with a slow relaxation of the magnetisation

2003

Reaction of [FeIII(bipy)(CN)4]¯ with fully solvated MII cations [M = Co (1) and Mn (2)] produces the isostructural bis double zigzag chains [[FeIII(bipy)(CN)4]2MII(H2O)]·MeCN·1/2H2O; 1 exhibits intrachain ferromagnetic and interchain antiferromagnetic couplings, slow magnetic relaxation and hysteresis effects. Luminita Marilena, Toma, Luminita.Toma@uv.es ; Lescouezec, Alain Francois Rodri, Alain.Lescouezec@uv.es ; Lloret Pastor, Francisco, Francisco.Lloret@uv.es ; Julve Olcina, Miguel, Miguel.Julve@uv.es

Cyanide-bridged Fe(III)–Co(II)CyanideUNESCO::QUÍMICA:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundMagnetizationMaterials ChemistryAntiferromagnetismIsostructuralHysteresis effectsCondensed matter physicsUNESCO::QUÍMICA::Química inorgánicaRelaxation (NMR)Metals and AlloysGeneral ChemistryCyanide-bridged Fe(III)–Co(II) ; Slow relaxation ; Ferromagnetic ; Antiferromagnetic ; Hysteresis effectsAntiferromagnetic:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyHysteresischemistryZigzagFerromagnetismFerromagneticCeramics and CompositesSlow relaxation
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A field induced ferromagnetic-like transition below 2.8 K in Li2CuO2: An experimental and theoretical study

1998

The low temperature magnetic properties of the Li2CuO2 compound have been investigated by means of superconducting quantum interference device magnetometry. We find in addition to an antiferromagnetic phase below 9.5 K a ferromagnetic-like steep rise of the magnetization around 2.8 K. The observed low temperature behavior is discussed by considering second and fourth order magnetocrystalline effective anisotropy coefficients, in addition to the exchange couplings reported in the literature. Work at the Institut de Ciencia dels Materials was supported by the Spanish Comisión Interministerial de Ciencia y Technología Grant No. CICYT MAT 96-1037.

Field (physics)MagnetometerExchange InteractionsGeneral Physics and AstronomyExchange Interactions (Electron)Magnetizationlaw.inventionMagnetizationMagnetisationAntiferromagnetism:FÍSICA [UNESCO]lawPhase (matter)Magnetic propertiesFerromagnetic MaterialsCopper OxidesLi2CuO2AntiferromagnetismAntiferromagnetic MaterialsLithium OxidesAnisotropyCondensed matter physicsTemperature Range 0000-0013 KChemistryTemperature DependenceUNESCO::FÍSICALithium Compounds ; Ferromagnetic-Antiferromagnetic Transitions ; Ferromagnetic Materials ; Antiferromagnetic Materials ; Magnetisation ; Magnetic Anisotropy ; Exchange Interactions (Electron) ; Lithium Oxides ; Copper Oxides ; Magnetization ; Exchange Interactions ; Antiferromagnetism ; Ferromagnetism ; Temperature Dependence ; Temperature Range 0000-0013 KMagnetic AnisotropyMagnetic anisotropyFerromagnetismLithium CompoundsFerromagnetismFerromagnetic-Antiferromagnetic TransitionsJournal of Applied Physics
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The key role of hydrogen bonding in the nuclearity of three copper(II) complexes with hydrazone-derived ligands and nitrogen donor heterocycles

2011

International audience; Three new Cu(II) complexes of formula [Cu(L1)(pyz)(CH3OH)]ClO4 (1), [Cu(L1)(4,4′-bpy)(ClO4)]·0.5H2O (2) and [{Cu(L2)(ClO4)}2(μ-4,4′-bpy)] (3) have been synthesised by using pyrazine (pyz) and 4,4′-bipyridine (4,4′-bpy) and tridentate O,N,O-donor hydrazone ligands, L1H and L2H, obtained by the condensation of 1,1,1-trifluoro-2,4-pentanedione with salicyloylhydrazide and benzhydrazide, respectively. The ligands and their complexes have been characterized by elemental analyses, FT-IR, and UV–Vis spectroscopies. Single crystal X-ray structure analysis evidences the metal ion in a slightly deformed square pyramidal geometry in all the complexes. However complexes 1 and 2 …

Hydrogen bondingDenticityPyrazineStereochemistryHydrazonechemistry.chemical_elementAntiferromagnetic couplingCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical SciencesMonodentate pyz and 4Physical and Theoretical ChemistryCu(II) hydrazone complexescopper complexhydrazone ligandchemistry.chemical_classificationhydrogen bondHydrogen bondSelf assemblyCopperSquare pyramidal molecular geometry0104 chemical sciencesCrystallographychemistryCrystal structures4′-bpySingle crystalhydrogen bond; copper complex; hydrazone ligand
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Spin canting in Re(IV) complexes: magnetic properties of [ReX4(bpym)] ( X = Cl and Br; bpym = 2,2′-bipyrimidine)

2008

The mononuclear complexes [ReCl4(bpym)] (1) and [ReBr4(bpym)] (2) (bpym = 2,2′-bipyrimidine) are weak ferromagnets. Magnetic ordering occurs below 7.0 (1) and 20.0 K (2) and good hysteresis loops are observed for the two compounds at 2.0 K. A spin-canting phenomenon, i.e., a non-strict linearity of the individual spins aligned in an anti-parallel way by intermolecular antiferromagnetic coupling occurring in many Re(IV) complexes, accounts for these magnetic features which are unusual in molecular solids such as 1 and 2.

HysteresisMolecular solidFerromagnetismCondensed matter physicsSpinsChemistryIntermolecular forceMaterials ChemistryPhysical and Theoretical ChemistryAntiferromagnetic couplingSpin cantingJournal of Coordination Chemistry
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Structural, magnetic and related attributes of some oximate-bridged tetranuclear nickel(ii) rhombs and a dinuclear congenerElectronic supplementary i…

2003

New oximate-bridged tetranuclear nickel(II) complexes of compositions {Ni(Dien)}2(μ3-OH)2{Ni2(Moda)4}(ClO4)2·Solv (Solv = H2O, 1a; Solv = 2CH3NO2, 1b; Solv = 2H2O·2C4H8O2, 1c), {Ni(Sdien)}2(μ3-OH)2{Ni2(Moda)4}(ClO4)2·H2O (2), {Ni(Odien)}2(μ3-OH)2{Ni2(Moda)4}(ClO4)2·0.6H2O (3), {Ni(Dien)}2(μ3-OH)2{Ni2(Inaf)4}(ClO4)2·CH3NO2 (4) and {Ni(Odien)}2(μ3-OH)2{Ni2(Inaf)4}(ClO4)2·2NaClO4·2H2O (5) and the dinuclear complex (Ni{Odien})2(Moda)2(ClO4)2 (6) have been prepared (Dien = 1,5-diamino-3-azapentane, Odien = 1,5-diamino-3-oxapentane, Sdien = 1,5-diamino-3-thiapentane, ModaH = butane-2,3-dione monooxime, InafH = phenylglyoxaldoxime). X-ray examination revealed similar structures for 1a, 1b, 1c, 2 a…

Inorganic ChemistryCrystallographyNickelFerromagnetismchemistryMagnetochemistryStereochemistryAntiferromagnetismchemistry.chemical_elementSpectroscopyCoupling (probability)Antiferromagnetic couplingDalton Transactions
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A Novel Dinuclear Fe II Spin‐Crossover Complex Based on a 2,2‐Bipyrimidine Bridge Ligand: [Fe(CH 3 bipy)(NCS) 2 ] 2 bpym

2004

The dinuclear iron(II) complex {[Fe(CH3bipy)(NCS)2]2bpym} has been synthesised and its crystal structure determined at 293 K. The magnetic properties display intramolecular antiferromagnetic coupling at 1 bar (J = −4.2 cm−1), and the onset of a pressure-induced spin conversion is observed at 11 kbar. Magnetic field Mossbauer measurements have been carried out at 4.2 K, and indicate that the HS species correspond to [HS-HS] pairs. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

Inorganic ChemistryCrystallographyNuclear magnetic resonanceLigandChemistrySpin crossoverIntramolecular forceMössbauer spectroscopyCrystal structureSpin (physics)Antiferromagnetic couplingMagnetic fieldEuropean Journal of Inorganic Chemistry
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Synthesis Crystal Structure and Magnetic Properties of the Trinuclear Nickel(II) Complex Bis[(μ-thiocyanato-N)bis(μ-pyridazine-N1,N2)bis(thiocyanato-…

2000

Unusual single N-bridging thiocyanato and double pyridazine (pdz) bridges occur in the linear trinuclear nickel(II) complex of formula [Ni3(pdz)6(NCS)6]. The compound exhibits a quasi Curie law behavior, the antiferromagnetic coupling through the double 1,2-diazine links being nearly compensated by the ferromagnetic exchange through the single N-bridging thiocyanato.

Inorganic chemistryPDZ domainchemistry.chemical_elementCrystal structureAntiferromagnetic couplingInorganic ChemistryPyridazinechemistry.chemical_compoundCrystallographyNickelCurie's lawchemistryFerromagnetismPhysical and Theoretical ChemistryInorganic Chemistry
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