Search results for "complexe"

showing 10 items of 920 documents

New coordination polymers based on a novel polynitrile ligand: Synthesis, structure and magnetic properties of the series [M(tcnoetOH)2(4,4′-bpy)(H2O…

2008

International audience; A novel polynitrile anionic ligand, tcnoetOH−(=[(NC)2CC(OCH2CH2OH)C(CN)2]−), has been synthesized by a one-pot reaction from a cyclic acetal and malononitrile. This ligand has been successfully used to prepare, with 4,4′-bpy as co-ligand, a novel series of coordination polymers formulated as [M(tcnoetOH)2(4,4′-bpy)(H2O)2] with M(II) = Fe (1), Co (2) and Ni (3). These isostructural compounds present a linear chain structure consisting of octahedrally coordinated metal ions bridged by trans 4,4′-bpy ligands. The coordination sphere of the metal ions is completed with two terminal tcnoetOH− ligand and two water molecules. The magnetic properties indicate that the three …

Transition metal complexesCoordination sphere010405 organic chemistryChemistryLigandMetal ions in aqueous solutionInorganic chemistryZero field splitting010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryParamagnetismCrystallographychemistry.chemical_compoundPolynitrileMagnetic propertiesMaterials ChemistryMolecule[CHIM]Chemical SciencesPhysical and Theoretical ChemistryIsostructuralChain complexesMalononitrile
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Relation entre transitivité et structure de communauté dans les réseaux complexes

2011

The relation between community structure and other topological properties in complex networks, has not been analyzed clearly. In this preliminary study, we explore experimentally the potential link between transitivity and community structure. We study the evolution of transitivity based on the quality of the community structure on artificially generated networks. Then we observe the evolution of community structure according to transitivity value. The results show a relationship between high transitivity and community structure. Additional analytical work is needed to identify the exact nature of this relationship.

Transitivité[ INFO.INFO-MO ] Computer Science [cs]/Modeling and SimulationRéseaux complexesStructure de communautés[INFO.INFO-MO] Computer Science [cs]/Modeling and Simulation[INFO.INFO-MO]Computer Science [cs]/Modeling and SimulationCoefficient de clustering
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Generator-based PET radiopharmaceuticals for molecular imaging of tumours: on the way to THERANOSTICS.

2011

Generator-derived radionuclides for PET/CT imaging are promising for optimizing targeted radiotherapy by an individual patient-based approach, applying pre-therapeutic evaluation, as well as dosimetric calculations, and for measuring treatment response after radionuclide therapy.

Treatment responsemedicine.medical_specialtyGenerator (computer programming)business.industryTargeted RadiotherapyInorganic ChemistryHeterocyclic Compounds 1-RingCoordination ComplexesMetalsNeoplasmsPositron-Emission TomographyRadionuclide therapyMedicineHumansMedical physicsMolecular imagingCt imagingRadiopharmaceuticalsbusinessNuclear medicineDalton transactions (Cambridge, England : 2003)
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Rational design and modelling of f-block molecular nanomagnets

2016

Los imanes monomoleculares o moléculas imán, por sus siglas en inglés SMMs, han suscitado una gran atención en los últimos años debido a sus extraordinarias propiedades físicas. Los cristales de este tipo de moléculas se caracterizan por presentar relajación lenta de la magnetización a baja temperatura, así como curvas de histeresis magnética. Estas moléculas se encuentran entre las entidades con comportamiento magnético más complejas, mostrando fenómenos cuánticos tales como efecto túnel en la magnetización, coherencia cuántica o interferencia cuántica. Por esto, se han postulado como candidatos prometedores para el diseño de bits cuánticos (qubits) de espín en computación cuántica. La pri…

UNESCO::FÍSICA::Electromagnetismo ::MagnetismoUNESCO::QUÍMICA::Química inorgánica ::Estructura de los compuestos inorgánicoslanthanides and actinides:FÍSICA::Electromagnetismo ::Magnetismo [UNESCO]:FÍSICA::Física del estado sólido ::Estados electrónicos [UNESCO]:FÍSICA::Física molecular::Moléculas inorgánicas [UNESCO]:QUÍMICA::Química inorgánica ::Estructura de los compuestos inorgánicos [UNESCO]UNESCO::QUÍMICA::Química inorgánica ::Compuestos de coordinaciónUNESCO::FÍSICA::Física molecular::Moléculas inorgánicas:QUÍMICA::Química inorgánica ::Compuestos de coordinación [UNESCO]computational chemistryquantum computingUNESCO::FÍSICA::Física del estado sólido ::Estados electrónicosmolecular nanomagnetism:QUÍMICA::Química inorgánica ::Tierras raras [UNESCO]coordination complexes:QUÍMICA::Química inorgánica ::Compuestos organometálicos [UNESCO]UNESCO::QUÍMICA::Química inorgánica ::Tierras rarasUNESCO::QUÍMICA::Química inorgánica ::Compuestos organometálicoscrystal field
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Novel inhibitors of mitochondrial respiratory chain: endoperoxides from the marine tunicate Stolonica socialis.

2001

The Mediterranean tunicate Stolonica socialis contains a new class of powerful cytotoxic acetogenins, generically named stolonoxides. In this paper, which also details the isolation and chemical characterization of a minor component (3a) of the tunicate extract, we report the potent inhibitory activity (IC(50) < 1 microM) of stolonoxides (1a and 3a) on mitochondrial electron transfer. The compounds affect specifically the functionality of complex II (succinate:ubiquinone oxidoreductase) and complex III (ubiquinol:cytochrome C oxidoreductase) in mammalian cells, thereby causing a rapid collapse of the whole energetic metabolism. This result, which differs from the properties of similar known…

UbiquinolMagnetic Resonance SpectroscopyStereochemistryIn Vitro TechniquesFunctional activityElectron Transportchemistry.chemical_compoundElectron Transport Complex IIIMarine Natural ProductOxidoreductaseMultienzyme ComplexesDrug DiscoveryMediterranean SeaAnimalsNADH NADPH OxidoreductasesUrochordataEnzyme InhibitorsFuranschemistry.chemical_classificationElectron Transport Complex IbiologyCytochrome cElectron Transport Complex IISuccinate dehydrogenaseElectron Transport Complex IIMyocardiumDioxolanesMitochondriaPeroxidesSuccinate DehydrogenaseMitochondrial respiratory chainchemistryBiochemistryElectron Transport Complex ICoenzyme Q – cytochrome c reductasebiology.proteinMolecular MedicineCattleStructure ElucidationOxidoreductasesJournal of medicinal chemistry
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Alix protein is substrate of Ozz-E3 ligase and modulates actin remodeling in skeletal muscle

2012

Alix/AIP1 is a multifunctional adaptor protein that participates in basic cellular processes, including membrane trafficking and actin cytoskeleton assembly, by binding selectively to a variety of partner proteins. However, the mechanisms regulating Alix turnover, subcellular distribution, and function in muscle cells are unknown. We now report that Alix is expressed in skeletal muscle throughout myogenic differentiation. In myotubes, a specific pool of Alix colocalizes with Ozz, the substrate-binding component of the muscle-specific ubiquitin ligase complex Ozz-E3. We found that interaction of the two endogenous proteins in the differentiated muscle fibers changes Alix conformation and pro…

Ubiquitin-Protein LigasesMuscle Fibers Skeletalmacromolecular substancesBiochemistryCell LineMiceCell MovementTwo-Hybrid System TechniquesmedicineCell AdhesionAnimalsProtein Interaction Domains and MotifsPseudopodiaMuscle SkeletalMolecular BiologyActinMice KnockoutbiologyMyogenesisSettore BIO/16 - Anatomia UmanaCalcium-Binding ProteinsUbiquitinationActin remodelingSkeletal muscleUbiquitin-Protein Ligase ComplexesCell BiologyActin cytoskeletonUbiquitin ligaseCell biologyRepressor ProteinsActin CytoskeletonProtein Transportmedicine.anatomical_structureUbiquitin ligase complexbiology.proteinCell Migration Myogenesis Skeletal Muscle Ubiquitin Ligase Ubiquitination Alix F-actin Ozz-E3 Ubiquitin Ligase Skeletal Muscle CellsCortactinCortactinProtein Binding
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Tri-alkenyl polyhedral oligomeric silsesquioxanes as comonomers and active center modifiers in ethylene copolymerization catalyzed by bis(phenoxy-imi…

2018

Abstract In copolymerization of ethylene (E) with tri-alkenyl-silsesquioxanes (POSS-6-3 and POSS-10-3) were used bis(phenoxy-imine) titanium, zirconium and vanadium catalysts, as well as salen-type vanadium catalysts. There were obtained copolymers with POSS-R-3 units as side branches of polymer chains. The type of employed bis(phenoxy-imine) titanium, zirconium and vanadium catalysts and salen-type catalyst of vanadium determined the copolymer chain termination reactions, as well as the mechanism of modification of the active species by the POSS-R-3 comonomer. POSS-R-3 comonomers caused selective poisoning of bis(phenoxy-imine) zirconium catalyst and they provided protection against tight …

V complexes salen-type complex of VImineActivationchemistry.chemical_elementVanadium02 engineering and technology010402 general chemistry01 natural sciencesCatalysissilsesquioxanes (POSS-R-3)CatalysisActive centerEthylenechemistry.chemical_compoundCopolymerizationPolymer chemistryCopolymerZirconiumTri-alkenyl polyhedral oligomericZrProcess Chemistry and TechnologyComonomerActive site modifier021001 nanoscience & nanotechnologyBis(phenoxy-imine) Ti0104 chemical scienceschemistry0210 nano-technologyTitaniumApplied Catalysis A: General
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Mixed‐valence trinuclear manganese clusters : Influence of the electronic transfer on the magnetic properties

1990

The magnetic behavior of mixed‐valence trinuclear clusters d4‐d4‐d5 is discussed on the basis of a model which takes into account valence delocalization and Heisenberg exchange. This model considers the competing effect between the electronic transfer and the localization of the extra electron due to an asymmetry of the triangular entity. The magnetic properties of the mixed‐valence oxo‐centered Mn(II)‐Mn(III)‐Mn(III) complexes formulated as Mn3O(O2CR)6L3 (R=Me, L=pyridine) are discussed on the basis of the developed model, supporting a significant intramolecular electron transfer. A comparison of these results to those previously reported by assuming a valence‐trapped model is given. Carlo…

Valence (chemistry)ChemistryMagnetic Propertiesmedia_common.quotation_subjectUNESCO::FÍSICAExchange InteractionsGeneral Physics and Astronomychemistry.chemical_elementManganeseElectronElectron TransferManganese ComplexesAsymmetryElectron transferCrystallographyDelocalized electronchemistry.chemical_compound:FÍSICA [UNESCO]Intramolecular forcePyridineMixed−Valence CompoundsAtomic ClustersAtomic physicsMixed−Valence Compounds ; Electron Transfer ; Magnetic Properties ; Atomic Clusters ; Manganese Complexes ; Exchange Interactionsmedia_common
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Oxovanadium(V) complexes with tripodal bisphenolate and monophenolate ligands: Syntheses, structures and catalytic activities

2019

Abstract The reactions between [VO(acac)2] (acac– = acetylacetonate) and the tripodal amino bisphenols 6,6′-(((2-morpholinoethyl)azanediyl)bis(methylene))bis(2,4-di-tert-butylphenol) (H2L1) and 6,6′-(((thiophen-2-ylmethyl)azanediyl)bis(methylene))bis(2,4-di-tert-butylphenol) (H2L2) as well as the tetradentate amino phenol 2,2′-((3,5-di-tert-butyl-2-hydroxybenzyl)azanediyl)bis(ethan-1-ol) (H3L3) afford the complexes [VO(L1)(OMe)] (1), [VO(L2)(acac)] (2) and [VO(L3)] (3), correspondingly. Complexes 1 and 3 can also be prepared using VOSO4·xH2O or [VO(OPr)3] as vanadium precursors. When [VO(acac)2] or VOSO4·xH2O is used, mononuclear oxovanadium(V) complexes are formed upon oxidation of the met…

Vanadiumchemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistrysulfoxidationCatalysisInorganic ChemistryMetalchemistry.chemical_compoundepoxidationcalculationsMaterials ChemistryPhysical and Theoretical ChemistryMethyleneta116Vanadium (V) complexes010405 organic chemistryChemistryThioanisolekompleksiyhdisteet0104 chemical sciencesTrigonal bipyramidal molecular geometryOctahedronvisual_artvisual_art.visual_art_mediumSingle crystalInorganica Chimica Acta
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Effects of Dissolved Complexation on REE Fate During Interactions between Volcanic Ash and Coexisting Fluids

2013

AbstractThis work analyzes REE behavior during the delivery of volcanic ash into a marine system and highlights the effects induced by dissolved carbonate and humate complexes on REE release. Kinetic experiments were carried out during a 6-month period using a batch method approach. Results show that the highest degree of REE leaching occurs during the early stage. Altered phases that crystallize induce REE sorption and dissolved complexation towards surface complexation, concurrent processes that are enhanced by Y/Ho, La/Yb, and Ce/Ce* changes, whereas dissolved humates and carbonates influence the dissolution rate of ash and the dissolved REE behavior.

Volcanic ash dissolutionEffect of dissolved complexesBatch methodGeochemistryEarth and Planetary Sciences(all)SorptionGeneral MedicineSurface complexationchemistry.chemical_compoundchemistryEnvironmental chemistryRare earth elements leachingCarbonateKinetic experimentsLeaching (metallurgy)DissolutionGeologygeochemistryVolcanic ashProcedia Earth and Planetary Science
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