Search results for "coordination complexes"

showing 10 items of 164 documents

Isomerism of [64Cu-NOTA-Bn]-labeled radiotracers: separation of two complex isomers and determination of their interconversion energy barrier using i…

2011

The model complex [(64)Cu((S)-p-NH(2)-Bn-NOTA)](-) ([(64)Cu]1) was used to study the isomerism of [(64)Cu-NOTA-Bn]-labeled radiotracers. Two complex isomers [(64)Cu]1a and [(64)Cu]1b, which were formed at a ratio of 1:9 during the complexation of [(64)Cu]Cu(2+) with (S)-p-NH(2)-Bn-NOTA, were separated using ion pair chromatography. To study the interconversion, the nonradioactive complex isomers Cu1a and Cu1b were separated and thermally treated at 90 °C in both ammonium acetate solution and deionized water. A faster interconversion rate was observed for both isomers with lower concentrations of ammonium ions. At the end of reaction, the thermodynamic Cu1a to Cu1b equilibrium ratio was 6:94…

Ion pair chromatographyAnalytical chemistryMolecular Conformationchemistry.chemical_elementAcetatesChemical Fractionation010402 general chemistry01 natural sciencesMolecular conformationIonInorganic Chemistrychemistry.chemical_compoundHeterocyclic Compounds 1-RingDrug StabilityIsomerismCoordination ComplexesHeterocyclic CompoundsAmmoniumPhysical and Theoretical ChemistryRadioactive TracersChromatography010405 organic chemistryChemistryChemical fractionationTemperatureWaterHydrogen-Ion ConcentrationCopper0104 chemical sciencesSolutionsPositron-Emission TomographyPhysical chemistryThermodynamicsAmmonium acetateCopperInorganic chemistry
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Intramolecular electron transfer between molybdenum and iron mimicking bacterial sulphite dehydrogenase

2014

Diferrocenyl/diferrocenium substituted dioxido molybdenum(VI) complexes [Fe2MoO2] 2(Fc)/[2(FC)]²⁺ mimic the catalytic active site including the redox subunits as well as the catalytic function of bacterial sulphite oxidases.

IronSulfite DehydrogenaseMolecular Conformationchemistry.chemical_elementBiocompatible MaterialsElectronsCrystallography X-RayPhotochemistryRedoxCatalysisCatalysisElectron TransportElectron transferCoordination ComplexesCatalytic DomainPolymer chemistryMaterials ChemistrySulfite dehydrogenaseFerrous CompoundsMolybdenumBacteriabiologyMetals and AlloysActive siteGeneral ChemistryElectron transport chainSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryMolybdenumIntramolecular forceCeramics and Compositesbiology.proteinOxidation-ReductionChemical Communications
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Lanthanide complexes as imaging agents anchored on nano-sized particles of boehmite

2011

International audience; The synthesis of boehmite nanoparticles modified with lanthanides (Eu, Tb and Gd) is described. Their synthesis, characterization and in vitro assays with HeLa cells were performed. The nuclear magnetic relaxation dispersion (NMRD) profiles of the two chelating moieties were studied. Imaging data from laser scanning confocal fluorescence microscopy and flow cytometry revealed that the nanoscaffolds were taken up by the cells, distributed throughout the cytoplasm and showed no toxicity. This platform could represent an alternative to silica-based inert matrices as imaging vehicles.

LanthanideBoehmiteGADOLINIUM(III) COMPLEXESRELAXIVITYConfocalEUROPIUMchemistry.chemical_elementNanoparticleMetal NanoparticlesAluminum Hydroxide02 engineering and technology010402 general chemistry01 natural sciencesLanthanoid Series ElementsPROBESInorganic ChemistryCoordination ComplexesMicroscopyFluorescence microscopeAluminum OxideNANOPARTICLESHumans[CHIM]Chemical SciencesParticle SizeCYCLEN COMPLEXESFluorescent DyesMicroscopy ConfocalMRI CONTRAST AGENTS021001 nanoscience & nanotechnologyFlow Cytometry0104 chemical scienceschemistryWATER-EXCHANGELUMINESCENCE0210 nano-technologyEuropiumLuminescenceEMISSIONNuclear chemistryHeLa Cells
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Coexistence of long-range antiferromagnetic order and slow relaxation of the magnetization in the first lanthanide complex of a 1,2,4-benzotriazinyl …

2017

The first lanthanide complex of a 1,2,4-benzotriazinyl radical (1), Dy(1)(tbacac)3 (2, tbacac = 2,2,6,6-tetramethyl-3,5-heptane-dionato), was synthesised and found to have an antiferromagnetically ordered ground state with a metamagnetic phase diagram and a critical field of 0.91 T at 1.85 K. The application of a small dc field revealed the single-molecule magnet behaviour of 2, illustrating the coexistence of long-range antiferromagnetic order and slow relaxation of the magnetization. peerReviewed

LanthanideCondensed matter physics010405 organic chemistryChemistryRelaxation (NMR)[CHIM.MATE]Chemical Sciences/Material chemistrykompleksiyhdisteetharvinaiset maametallit010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic ChemistryMagnetizationMagnetmagnetismAntiferromagnetismcoordination complexesmagnetismiGround staterare earth metalsCritical fieldta116ComputingMilieux_MISCELLANEOUSPhase diagram
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Thermal expansion and magnetic properties of benzoquinone-bridged dinuclear rare-earth complexes.

2017

The synthesis and structural characterization of two benzoquinone-bridged dinuclear rare-earth complexes [BQ(MCl2·THF3)2] (BQ = 2,5-bisoxide-1,4-benzoquinone; M = Y (1), Dy (2)) are described. Of these reported metal complexes, the dysprosium analogue 2 is the first discrete bridged dinuclear lanthanide complex in which both metal centres reside in pentagonal bipyramidal environments. Interestingly, both complexes undergo significant thermal expansion upon heating from 120 K to 293 K as illustrated by single-crystal X-ray and powder diffraction experiments. AC magnetic susceptibility measurements reveal that 2 does not show the slow relation of magnetization in zero dc field. The absent of …

Lanthanidemagneettiset ominaisuudetStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesInorganic ChemistryMagnetizationPentagonal bipyramidal molecular geometryAb initio quantum chemistry methodsheat expansioncoordination complexesrare earth metalsta116010405 organic chemistrykompleksiyhdisteetharvinaiset maametallitBenzoquinoneMagnetic susceptibility0104 chemical sciencesCrystallographychemistryDysprosiummagnetic propertiesPowder diffractionlämpölaajeneminenDalton transactions (Cambridge, England : 2003)
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A dinucleating ligand which promotes DNA cleavage with one and without a transition metal ion.

2013

The dinucleating ligand L (1,3-bis[bis(pyridin-2-ylmethyl)amino]propan-2-ol) combined with metal ions efficiently cleaves DNA when M : L is 1 : 1 (M = Co(II) or Fe(III)) at pH 5.5–7.0, with free L being more active at acidic pH than when bound to Zn(II), Cu(II) or Ni(II) at neutral pH.

LigandPyridinesMetal ions in aqueous solutionInorganic chemistryMetals and AlloysGeneral ChemistryDNALigandsTransition metal ionsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryDna cleavageCoordination ComplexesPolymer chemistryMaterials ChemistryCeramics and CompositesTransition ElementsNeutral phDNA CleavageDNAPlasmidsChemical communications (Cambridge, England)
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Fluorescent metal-based complexes as cancer probes.

2020

Abstract The ability to track drugs inside of cells and tumours has been highly valuable in cancer research and diagnosis. Metal complexes add attractive features to fluorescent drugs, such as targeting and specificity, solubility and uptake or photophysical properties. This review focuses on the latest fluorescent metal-based complexes, their cellular targets, photophysical properties and possible anticancer effects.

LightClinical BiochemistryPharmaceutical ScienceAntineoplastic Agents01 natural sciencesBiochemistryMetal-based probesMetalMetal complexesCoordination ComplexesCell Line TumorMetals HeavyNeoplasmsDrug DiscoveryAnticancer probesFluorescence microscopemedicineAnimalsHumansSolubilityMolecular BiologyFluorescent DyesFluorescence microscopyTargeting010405 organic chemistryChemistryOrganic ChemistryCancermedicine.diseaseTheranosticsCombinatorial chemistryFluorescence0104 chemical sciences010404 medicinal & biomolecular chemistryvisual_artvisual_art.visual_art_mediumFluorescent probesMolecular MedicineBioorganicmedicinal chemistry letters
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Dual Labeling of Lipopolysaccharides for SPECT-CT Imaging and Fluorescence Microscopy.

2013

International audience; : Lipopolysaccharides (LPS) or endotoxins are amphipathic, pro-inflammatory components of the outer membrane of Gram-negative bacteria. In the host, LPS can trigger a systemic inflammatory response syndrome. To bring insight into in vivo tissue distribution and cellular uptake of LPS, dual labeling was performed with a bimodal molecular probe designed for fluorescence and nuclear imaging. LPS were labeled with DOTA-Bodipy-NCS, and pro-inflammatory properties were controlled after each labeling step. LPS were then radiolabeled with (111)In and subsequently injected intravenously into wild-type, C57B16 mice, and their in vivo behavior was followed by single photon emis…

LipopolysaccharidesBiodistribution[CHIM.THER]Chemical Sciences/Medicinal Chemistry[ SDV.BBM.BM ] Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biology010402 general chemistry01 natural sciencesBiochemistryLipopolysaccharide transport03 medical and health sciencesMiceIn vivoCoordination ComplexesFluorescence microscope[INFO.INFO-IM]Computer Science [cs]/Medical ImagingAnimals[CHIM.COOR]Chemical Sciences/Coordination chemistryTissue Distribution030304 developmental biologyFluorescent DyesTomography Emission-Computed Single-Photon0303 health sciencesMolecular Structure[ INFO.INFO-IM ] Computer Science [cs]/Medical ImagingChemistryIndium Radioisotopes[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biology[ CHIM.THER ] Chemical Sciences/Medicinal ChemistryGeneral MedicineFluorescence0104 chemical sciencesMice Inbred C57BLMicroscopy FluorescenceIsotope LabelingBiophysicsMolecular Medicinelipids (amino acids peptides and proteins)Bacterial outer membraneMolecular probe[CHIM.RADIO]Chemical Sciences/Radiochemistry[ CHIM.RADIO ] Chemical Sciences/RadiochemistryEx vivo
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Gold nanostars co-coated with the Cu(II) complex of a tetraazamacrocyclic ligand

2015

The twelve-membered tetraazamacrocyclic ligand L1 bears an appended lipoic acid unit, whose disulphide ring is an efficient grafting moiety for the surface of gold nanostars (GNS). The GNS that were used featured a localized surface plasmon resonance (LSPR) absorption at ∼800 nm, i.e. in the near infrared (NIR). We investigated different approaches for coating them with the Cu(2+) complex of L1. While the direct reaction of [CuL1](2+) with as-prepared GNS led to aggregation, an initial coating step with polyethyleneglycol-thiol (PEG-SH) was found to be advantageous. Displacement reactions were carried out on pegylated GNS either with [CuL1](2+), directly generating [Cun(L1@GNS)](2n+), or wi…

LuminescenceLuminescent AgentsMacrocyclic CompoundsGole nanoparticelle Cooper macrocyclesStereochemistryChemistryKineticsMetal NanoparticlesPet imagingSurface Plasmon Resonanceengineering.materialPhotothermal therapyCyclamsInorganic ChemistryCrystallographyTransmetalationCoatingCoordination ComplexesHeterocyclic CompoundsengineeringMoietyGoldSurface plasmon resonanceLuminescenceCopper
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Holmium(III) Single-Ion Magnet for Cryomagnetic Refrigeration Based on an MRI Contrast Agent Derivative

2021

The coexistence of field-induced blockage of the magnetization and significant magnetocaloric effects in the low-temperature region occurs in a mononuclear holmium(III) diethylenetriamine-N,N,N′,N″,N″-pentaacetate complex, whose gadolinium(III) analogue is a commercial MRI contrast agent. Both properties make it a suitable candidate for cryogenic magnetic refrigeration, thus enlarging the variety of applications of this simple class of multifunctional molecular nanomagnets.

MRI contrast agentGadoliniumCommunicationMagnetic PhenomenaRefrigerationchemistry.chemical_elementPentetic AcidInorganic ChemistryCold TemperatureMagnetizationchemistry.chemical_compoundHolmiumNuclear magnetic resonancechemistryCoordination ComplexesRefrigerationMagnetMagnetic refrigerationMagnetsPhysical and Theoretical ChemistryHolmiumDerivative (chemistry)Inorganic Chemistry
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