Search results for "Ferro"

showing 10 items of 2451 documents

Effect of Protonated Organic Cations and Anion−π Interactions on the Magnetic Behavior of Hexabromorhenate(IV) Salts

2015

Two novel Re-IV compounds of formula (Hbpym)(2)[(ReBr6)-Br-IV]center dot 4H(2)O (1) and (H(4)biim)[(ReBr6)-Br-IV]center dot 4H(2)O (2) [Hbpym(+) = 2,2'-bipyrimidinium cation and H(4)biim(2+) = 2,2'-biimidazolium dication] have been prepared and magnetostructurally characterized. 1 and 2 exhibit distinct crystal packing, and the presence of weak intermolecular contacts, such as Re-Br...B-rRe (1 and 2), Re-Br center dot center dot center dot(H2O)center dot center dot center dot BrRe (1 and 2), and Re-Br center dot center dot center dot pi center dot center dot center dot Br-Re (2), lead to different magnetic behaviors. While 1 is antiferromagnetic, 2 is a ferromagnetic compound and indeed the…

chemistry.chemical_classificationStereochemistryIntermolecular forceSalt (chemistry)ProtonationGeneral ChemistryCondensed Matter Physics3. Good healthDicationIonCrystalCrystallographychemistryFerromagnetismAntiferromagnetismCOMPLEXESGeneral Materials ScienceX-RAY-STRUCTURECrystal Growth & Design
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Molecular squares of Ni(II) and Cu(II): ferromagnetic exchange interaction mediated by syn-anti carboxylate-bridging.

2009

The synthesis of four discrete tetranuclear complexes {[Ni(II)(L(2))][ClO(4)]}(4).MeCN (1), {[Cu(II)(L(1))(O(3)SCF(3))]}(4).H(2)O (), {[Cu(II)(L(3))(OClO(3))]}(4).MeCN () and {[Cu(II)(L(4))][ClO(4)]}(4).3MeCN.4H(2)O (4), supported by a closely similar group of carboxylate-appended (2-pyridyl)alkylamine ligands [L(1)(-): 3-[N-methyl-{2-(pyridin-2-yl)ethyl}amino]propionate; L(2)(-): 3-[(2-(pyridin-2-yl)ethyl){2-(pyridin-2-yl)methyl}amino]propionate; L(3)(-): 3-[N-isopropyl-{2-(pyridin-2-yl)methyl}amino]propionate and L(4)(2-): 3-[N-{2-(pyridin-2-yl)methyl}amino]-bis(propionate)] is described. Structural characterization reveals that each Ni(II) centre in 1 has square-pyramidal Ni(II)N(3)O(2) …

chemistry.chemical_classificationStereochemistryLigandExchange interactionIonInorganic Chemistrychemistry.chemical_compoundCrystallographyOxygen atomchemistryFerromagnetismPropionateMoleculeCarboxylateDalton transactions (Cambridge, England : 2003)
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Syntheses, crystal structures and magnetic properties of a series of μ-phenoxo-μ1,1-carboxylato-μ1,3-carboxylato trinickel(II) compounds.

2014

The work in this report describes the syntheses, characterization, crystal structures and magnetic properties of eight linear trinickel(ii) compounds of the composition [Ni(II)3(L(sal-pyr))2(propionate)4] (), [Ni(II)3(L(sal-pyr))2(benzoate)4]·CH3CN (), [Ni(II)3(L(sal-pip))2(acetate)4]·2CH3CN (), [Ni(II)3(L(sal-pip))2(propionate)4] (), [Ni(II)3(L(sal-pip))2(benzoate)4]·CH2Cl2 (), [Ni(II)3(L(sal-mor))2(propionate)4] (), [Ni(II)3(L(sal-mor))2(benzoate)4]·3CH2Cl2 () and [Ni(II)3(L(sal-mor))2(o-Cl-benzoate)4]·2CH3CN·2H2O (), where HL(sal-pyr), HL(sal-pip) and HL(sal-mor) are the 1 : 1 condensation products of salicylaldehyde and 1-(2-aminoethyl)-pyrrolidine, 1-(2-aminoethyl)-piperidine and 4-(2-…

chemistry.chemical_classificationStereochemistrychemistry.chemical_elementCrystal structureInorganic ChemistryMetalMagnetizationchemistry.chemical_compoundCrystallographyNickelFerromagnetismSalicylaldehydechemistryvisual_artvisual_art.visual_art_mediumPropionateMoietyDalton transactions (Cambridge, England : 2003)
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Ferromagnetic coupling in a one-dimensional molecular railroad copper(II) azido compound containing a defective double cubane motif.

2001

The compound [Cu2(bpm)2(N3)4]n (bpm = bis(pyrazol-1−yl)methane) shows three unique coordination modes (μ1,1-, μ1,1,1-, μ1,1,3-N3) and ferromagnetic interaction between the copper(II) ions. The structure of the compound exhibits a one-dimensional railroad polymer made up of repeating defective dicubane-type units linked by μ1,1,3-N3 bridges.

chemistry.chemical_classificationStereochemistrychemistry.chemical_elementPolymerCopperIonInorganic ChemistryCoupling (electronics)chemistry.chemical_compoundCrystallographychemistryFerromagnetismCubanePhysical and Theoretical ChemistryInorganic chemistry
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Restricted rotation in unbridged sandwich complexes: rotational behavior of closo-[Co(eta 5-NC4H4)(C2B9H11)] derivatives.

2005

Rotation about the centroid/ metal/centroid axis in ferrocene is facile; the activation energy is 1-5 kcal mol - 1 . The structurally similar sandwich complexes derived from closo-[3-Co(η 5 -NC 4 H 4 )-1,2-C 2 B 9 H 1 1 ] (1) have a different rotational habit. In 1, the cis rotamer in which the pyrrolyl nitrogen atom bisects the carboranyl cluster atoms is 3.5 kcal mol - 1 more stable in energy than the rotamer that is second lowest in energy. This cis rotamer is wide, spanning 216°, and may be split into three rotamers of almost equal energy by substituting the N and the carboranyl carbon atoms adequately. To support this statement, closo-[3-Co(η 5 -NC 4 H 4 )-1,2-(CH 3 ) 2 -1,2-C 2 B 9 H …

chemistry.chemical_classificationSteric effects010405 organic chemistryStereochemistryOrganic ChemistryHeteroatomGeneral Chemistry010402 general chemistry7. Clean energy01 natural sciencesCatalysis0104 chemical sciencesRotational energyIonElectronegativitychemistry.chemical_compoundCrystallographychemistryFerroceneCounterionConformational isomerismChemistry (Weinheim an der Bergstrasse, Germany)
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Pentachloro(pyrazine)rhenate(iv) complex as precursor of heterobimetallic pyrazine-containing ReIV2MII (M = Ni, Cu) species: synthesis, crystal struc…

2008

Three novel Re(IV) mononuclear complexes of formulae NBu4[ReC15(pyz)] (1), NH2Me2[ReCl5(pyz)] (2) and NH4[ReCl5(pyz)].0.75H2O (3), (pyz being pyrazine; NBu4+ = tetra-n-butylammonium cation, NH2Me2+ = dimethylammonium cation and NH4+ = ammonium cation), were synthesized by ligand substitution reaction from [ReCl6]2- anion and pyrazine in N,N-dimethylformamide (DMF). In addition, two new heterobimetallic compounds, the salt namely [ReCl5(pyz)]2[Ni(cyclam)](4) (cyclam = 1,4,8,11-tetraazacyclotetradecane) and the heterotrinuclear [{ReCl5(mu-pyz)}2Cu(DMF)4] (5) complex, were prepared by using as precursor 1 and 3, respectively. Compounds 1-5 were characterized by single-crystal X-ray diffraction…

chemistry.chemical_classificationSubstitution reactionPyrazineLigandMetal ions in aqueous solutionInorganic chemistrySalt (chemistry)Crystal structureInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryCyclamAntiferromagnetismDalton Transactions
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Enantioselective self-assembly of antiferromagnetic hexacopper(ii) wheels with chiral amino acid oxamates

2013

The Cu(2+)-mediated self-assembly of oxamato-based ligands derived from either the (S)- or (R)-enantiomers of the amino acid valine leads to the formation of two antiferromagnetically coupled homochiral anionic hexacopper(II) wheels in the presence of templating tetramethylammonium countercations.

chemistry.chemical_classificationTetramethylammoniumStereochemistryMagnetic PhenomenaMetals and AlloysEnantioselective synthesisStereoisomerismValineGeneral ChemistryLigandsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidchemistry.chemical_compoundchemistryCoordination ComplexesValineMaterials ChemistryCeramics and CompositesAntiferromagnetismSelf-assemblyCopperChemical Communications
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Exploring the exchange interaction in a mixed valence {CoII4CoIII2} hexanuclear cluster with novel topology

2012

Abstract Reaction between [Co2(μ-OH2)(μ-Piv)2(Piv)2(HPiv)4] and a (salicylidene)ethanolamine ligand under ambient reaction conditions, affords hexanuclear complexes [CoIII2CoII4(Piv)8(HPiv)2(L)2(OH)2] (1–2). Both products have been characterized crystallographically and found to be mixed-valent, containing divalent and trivalent Co centers. Down to 30 K, the variable-temperature magnetic susceptibility data are dominated by the single-ion properties of high spin Co(II) centers with distorted-octahedral coordination geometries. Below this temperature, the effect of intramolecular ferromagnetic exchange interactions becomes apparent. Magnetic data has been analyzed in terms of ground isolated…

chemistry.chemical_classificationValence (chemistry)ChemistryExchange interactionCrystal structureMagnetic susceptibilityDivalentInorganic ChemistryMagnetizationCrystallographyFerromagnetismIntramolecular forceMaterials ChemistryPhysical and Theoretical ChemistryPolyhedron
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Pressure effect studies in molecular magnetism

2004

We report on temperature dependent magnetic susceptibility and Mossbauer effect studies of the influence of hydrostatic pressure (up to 1.2 GPa) on dynamic electronic structure phenomena in 3d transition metal coordination compounds. The systems under investigation are mononuclear spin crossover compounds of iron (II) and chromium (II), dinuclear complexes of iron (II) exhibiting coexistence of intramolecular antiferromagnetic coupling and thermal spin crossover, 1D, 2D and 3D polynuclear spin crossover complexes of iron (II), a valence tautomeric system of cobalt (II) showing a thermal transition from a high spin [CoII (semiquinone)] to a low spin [CoII (catecholate)] species on lowering t…

chemistry.chemical_classificationValence (chemistry)Condensed matter physicsChemistryMagnetismGeneral Chemical EngineeringHydrostatic pressureGeneral ChemistryCondensed Matter PhysicsMagnetic susceptibilityCoordination complexCrystallographyElectron transferFerromagnetismTransition metalSpin crossoverCondensed Matter::Strongly Correlated ElectronsGeneral Materials ScienceJournal of Physics: Condensed Matter
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Synthesis, characterization and magnetic properties of mixed-valence iron complexes with 2-pyridyl oximes

2018

Two new mixed-valence iron complexes with 2-pyridyl oximes, [Fe(mpko)3Fe(H2O)2(NO3)](NO3)·2H2O (1) (mpko− = methyl(2-pyridyl)ketone oximate) and [{Fe(dpko)3}2Fe](ClO4)·4H2O (2) (dpko− = bis(2-pyridyl)ketone oximate), have been prepared by reaction of FeIII with mpkoH in methanol (1) and FeII with dpkoH in methanol/water (2). Dinuclear FeII(low-spin)FeIII(high-spin) and trinuclear FeII(low-spin)FeIII(high-spin)FeII(low-spin) cations are present in the crystal structure of 1 and 2, respectively. Intermolecular hydrogen bonds in 1 lead to weak antiferromagnetic interactions between pairs of neighboring FeIII centers, which allows observation of single-ion zero-field splitting effects.

chemistry.chemical_classificationValence (chemistry)Ketone010405 organic chemistryChemistryHydrogen bondIntermolecular forceCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesMethyl 2-pyridyl ketone oximechemistry.chemical_compoundCrystallographyMaterials ChemistryAntiferromagnetismMethanolPhysical and Theoretical Chemistry
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