Search results for "cobalt."

showing 10 items of 969 documents

On/Off Photoswitching in a Cyanide-Bridged {Fe2Co2} Magnetic Molecular Square

2013

International audience; A repeatable bidirectional paramagnetic ↔ diamagnetic photomagnetic effect has been observed in the cyanide-bridged Fe-Co square complex {[Fe{B(pz)(4)}(CN)(3)](2)[Co(bik)(2)](2)}(ClO(4))(2)*3H(2)O [B(pz)(4) = tetrapyrazolylborate, bik = bis(1-methylimidazol-2-yl)ketone]. Magnetic measurements and low-temperature single-crystal X-ray diffraction experiments have shown that a complete electron transfer from the diamagnetic Fe(II)-Co(III) state to the paramagnetic Fe(III)-Co(II) metastable state is induced by 808 nm laser light irradiation, whereas the diamagnetic state is recovered in an almost quantitative yield under irradiation at 532 nm.

CyanideINDUCED ELECTRON-TRANSFERTRANSITIONSRELAXATION010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCOBALT-IRON CYANIDECatalysisPHOTOINDUCED MAGNETIZATIONParamagnetismchemistry.chemical_compoundElectron transferColloid and Surface ChemistryMetastability[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyIrradiationALKALI-METAL-IONPRUSSIAN BLUE ANALOGS010405 organic chemistryChemistryRelaxation (NMR)Photomagnetic effectGeneral Chemistry3. Good health0104 chemical sciencesCOSOLID-STATECrystallographyDiamagnetismJournal of the American Chemical Society
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Cascade complex formation by phosphate in the cobalt(II)/[30]aneN10 anaerobic system

1993

Abstract The interaction of phosphate with the mono- and binuclear cobalt(II) complexes of [30]aneN 10 (1,4,7,10,13,16,19,22,25,28-decaazacyclotriacontane) has been studied by potentiometry in 0.15 mol dm −3 NaClO 4 solution at 298.15 K under anaerobic conditions. The stable species [CoH 2 ([30]aneN 10 )PO 4 ] + , [CoH 4 ([30]aneN 10 )PO 4 ] 3+ , [Co 2 H([30]aneN 10 )PO 4 ] 2+ , [Co 2 H 2 ([30]aneN 10 )PO 4 ] 3+ and [Co 2 H 3 ([30]aneN 10 )PO 4 ] 4+ , where the phosphate anion is directly bound to the metal ions or acts as a second sphere ligand, are formed and their stability constants have been determined. The results obtained allowed for the selection of suitable conditions for the study…

DIOXYGEN CARRIERS; DIOXYGEN BINDING; Co(II) COMPLEXES; POLYAMINE LIGANDS; DITOPIC POLYAMINES; OPEN-CHAIN POLYAZAALKANES; THERMODYNAMICS; ANION COORDINATION CHEMISTRY; INCLUSION COMPLEXESINCLUSION COMPLEXESMetal ions in aqueous solutionComplex formationInorganic chemistryDIOXYGEN BINDINGchemistry.chemical_elementMedicinal chemistryCo(II) COMPLEXESInorganic Chemistrychemistry.chemical_compoundOPEN-CHAIN POLYAZAALKANESANION COORDINATION CHEMISTRYTHERMODYNAMICSMaterials ChemistryDIOXYGEN CARRIERSPhysical and Theoretical ChemistryLigandPhosphatePhosphate anionchemistryDITOPIC POLYAMINESChemical equilibriumAnaerobic exerciseCobaltPOLYAMINE LIGANDS
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Slow Magnetic Relaxation in a Co (II)–Y (III) Single‐Ion Magnet with Positive Axial Zero‐Field Splitting

2013

This work was supported by the MINECO (Spain) (Project CTQ2011-24478), the Junta de Andalucía (FQM-195 and Project of excellence P08-FQM-03705), and the University of Granada. E.R. and E.Cr. thank MINECO grant No. CTQ2011-23862-C02-01 and Generalitat de Catalunya grant No. 2009SGR-1459, for financial support. We would like to thank Prof. Liviu Chibotaru for providing us the SINGLE_ANISO program and Dr. Andrew Ozarowski for the EPR simulation software. E.K.B. thanks the EPSRC and Leverhulme Trust for financial support. The NHMFL is funded by the NSF, DoE, and the state of Florida. J.C. acknowledges financial support by the Spanish Ministerio de Ciencia e Innovación through projects CTQ2010-1…

DYNAMICSModels Molecularpositive zero-field splittingINSchemistry.chemical_elementZero field splitting010402 general chemistry01 natural sciences7. Clean energyCatalysisO ligandsMOLECULE MAGNETNuclear magnetic resonancesingle ion magnetsYttriumMagnetic relaxationCompartmental ligandAnisotropyHYSTERESISComputingMilieux_MISCELLANEOUSANISOTROPY[PHYS]Physics [physics]IonsMolecular StructureCondensed matter physicsSingle ion010405 organic chemistryChemistryCobaltGeneral ChemistryYttriumNBARRIERcobaltCo(II)FAMILY0104 chemical sciencesyttriumHysteresisPositive axial ZFSDYSPROSIUM(III)TBMagnetic FieldsMagnetMagnetsSingle ion magnetCOMPLEXESCobaltBEHAVIOR
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Heterometallic CoII-CoIII-MII alkoxido-bridged heptanuclear motifs (M = Cu, Zn). Syntheses, crystal structures and magnetic properties

2018

Two new alkoxido-bridged heterometallic complexes of formula [CoIICoIII 3CuII 3(dea)6(CH3COO)3](ClO4)0.75(CH3COO)1.25 (1) and [CoII 2CoIII 2ZnII 3(tea)2(piv)6(CH3O)2(OH)2(CH3OH)2]·H2O 2 (H2dea=diethanolamine, H3tea=triethanolamine and Hpiv=pivalic acid) have been assembled using aminoalcohol ligands. The cationic core in 1 possesses a threefold crystallographic axis, and it exhibits a set of three copper(II), one cobalt(II) and three cobalt(III) ions arranged as a hexagon of alternating copper(II) and cobalt(III) ions around the central cobalt(II) ion. Each edge of the hexagon is defined by a double alkoxido bridge, the outer one being bis-monodentate with copper(II)-cobalt(III) pair wherea…

Denticity/dk/atira/pure/subjectarea/asjc/2500/2505Inorganic chemistrychemistry.chemical_elementCrystal structureZinc010402 general chemistry01 natural sciencesCobalt complexesIonInorganic ChemistryMagnetic propertiesZinc complexesMaterials ChemistryPhysical and Theoretical Chemistry/dk/atira/pure/subjectarea/asjc/1600/1606/dk/atira/pure/subjectarea/asjc/1600/1604010405 organic chemistryLigandCopper0104 chemical sciencesCrystallographychemistryIntramolecular forceMixed-valence clustersCobaltCopper complexesInorganica Chimica Acta
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Acetazolamide-M(II) [M(II) = Co(II), Ni(II), Cu(II)] complexes with ethylamine, diethylamine, triethylamine, and potassium hidroxide

1991

Abstract Complexes of Co(II), Ni(II), and Cu(II) with dideprotonated Acm are synthesized and characterized. Acm acts as bidentate ligand through the N-sulfonamido atom and the N-thiadiazole atom except for K6CoAcm4·6H2O in which Acm behaves as monodentate through the N-sulfonamido atom.

DenticityDiethylaminesPotassium CompoundsPotassiumInorganic chemistrychemistry.chemical_elementLigandsBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundNickelEthylaminesHydroxidesmedicineTriethylamineDiethylamineChemistrySpectrophotometry AtomicCobaltAcetazolamideSpectrophotometryPotassiumEthylamineAcetazolamideCoppermedicine.drugJournal of Inorganic Biochemistry
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Novel cobalt(II) coordination polymers based on 1,2,4,5-benzenetetracarboxylic acid and extended bis-monodentate ligands

2009

Four new high-spin cobalt(II) complexes of formulae [Co2(bta)(4,4′-bpy)2(H2O)2]n (1), {Hbpe[Co(Hbta)(bpe)(H2O)2]}n (2), {[Co(H2bta)(azpy)(H2O)2]·azpy}n (3) and {[Co2(bta)(bpa)2(H2O)4]·8H2O}n (4) with H4bta = 1,2,4,5-benzenetetracarboxylic acid, 4,4′-bpy = 4,4′-bipyridine, bpe = trans-1,2-bis(4-pyridyl)ethene, azpy = 4,4′-azobispyridine and bpa = trans-1,2-bis(4-pyridyl)ethane, have been prepared and characterized by single crystal X-ray diffraction. Compounds 1–4 exhibit two-dimensional networks where the fully (1 and 4) or partially (2 and 3) deprotonated tetracarboxylic ligand connects two (2 and 3) or four (1 and 4) cobalt(II) ions through two trans-carboxylate (1–3) or all the carboxyla…

DenticityLigandInorganic chemistrychemistry.chemical_elementGeneral ChemistryCondensed Matter Physicschemistry.chemical_compoundCrystallographyDeprotonationchemistryOctahedronMoleculeGeneral Materials ScienceCarboxylateCobaltSingle crystalCrystEngComm
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Experimental and Computational Study of Unique Tetranuclear µ 3 ‐Chloride and µ‐Phenoxo/Chloro‐Bridged Defective Dicubane Cobalt(II) Clusters

2016

Two tetranuclear CoII clusters [Co4(L)2(µ3-Cl)2Cl2] have been prepared by using multidentate diaminobisphenolate ligands. The solid-state structures of the complexes were determined by single-crystal X-ray diffraction. The cores of the cluster compounds can be defined as a two-vertex-deficient dicubane geometry (pseudo-dicubane). In the central unit, the cobalt(II) cations are linked through phenoxide oxygen (outer bridges) and chloride anions (inner bridges), previously unprecedented in this type of cobalt cluster. The magnetic properties were studied by both experimental and computational methods. By using a combination of techniques, we were able to determine the nature and strength of t…

DenticityStereochemistryChemistrychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologycobalt01 natural sciencesChloride0104 chemical sciencesMagnetic exchangeInorganic ChemistryCrystallographyCentral unitIntramolecular forcedensity functional calculationsmedicineCluster (physics)cluster compoundsmagnetic properties0210 nano-technologyta116Cobaltmedicine.drugEuropean Journal of Inorganic Chemistry
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Analyser of chromium and/or cobalt

2003

Abstract Two stopped-flow manifolds have been proposed for individual or simultaneous determination of chromium and cobalt in water samples. Automated procedures based on multicommutation systems have emphasised the differences of their catalytic effect in luminol–hydrogen peroxide chemiluminescence reaction. A more rapid decay of signal was observed for Co for both configurations (flow injection or continuous injection). The influence of chemical and hydrodynamic variables has been studied in order to establish the robustness of method. The analysis rate was lower 1.5 min per replicate. Chemometric tools have been employed for the resolution of their contributions. Partial least squares (P…

Detection limitAnalyserAnalytical chemistrychemistry.chemical_elementBiochemistryAnalytical ChemistryChemometricsChromiumCertified reference materialschemistryStandard additionPartial least squares regressionEnvironmental ChemistryCobaltSpectroscopyAnalytica Chimica Acta
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Apoferritin-encapsulated Ni and Co superparamagnetic nanoparticles

2006

Ni and Co nanoparticles (average diameters 3 and 3.5 nm) have been prepared within the apoferritin cavity. The protein shell prevents bulk aggregation of the metal particles, rendering them water soluble. X-Ray diffraction, transmission electronic microscopy and magnetization measurements have been used for characterizing the nanoparticles. The magnetic study of both nanoparticles confirmed the expected superparamagnetic behavior.

DiffractionMaterials sciencechemistry.chemical_elementNanoparticleNanotechnologyGeneral Chemistryequipment and suppliesMetalMagnetizationNickelchemistryChemical engineeringvisual_artMaterials Chemistryvisual_art.visual_art_mediumMagnetic nanoparticleshuman activitiesCobaltSuperparamagnetismJ. Mater. Chem.
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Pressure-Driven Symmetry-Preserving Phase Transitions in Co(IO3)2

2021

[EN] High-pressure synchrotron X-ray diffraction studies of cobalt iodate, Co(IO3)(2), reveal a counterintuitive pressure-induced expansion along certain crystallographic directions. High-pressure Raman and infrared spectroscopy, combined with density-functional theory calculations, reveal that with increasing pressure, it becomes energetically favorable for certain I-O bonds to increase in length over the full range of pressure studied up to 28 GPa. This phenomenon is driven by the high-pressure behavior of iodate ion lone electron pairs. Two pressure-induced isosymmetric monoclinic-monoclinic phase transitions are observed at around 3.0 and 9.0 GPa, which are characterized by increasing o…

DiffractionPhase transitionElectron pairMaterials sciencechemistry.chemical_elementInfrared spectroscopySynchrotronSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionsymbols.namesakechemistry.chemical_compoundGeneral EnergychemistrylawChemical physicsFISICA APLICADAsymbolsPhysical and Theoretical ChemistryRaman spectroscopyCobaltIodateThe Journal of Physical Chemistry C
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