Search results for "ion chemistry"

showing 10 items of 254 documents

Tripyridinophane Platform Containing Three Acetate Pendant Arms: An Attractive Structural Entry for the Development of Neutral Eu(III) and Tb(III) Co…

2020

We report a detailed characterization of Eu3+ and Tb3+ complexes derived from a tripyridinophane macro cycle bearing three acetate side arms (H3tpptac). Tpptac3- displays an overall basicity (Σ log KiH) of 24.5, provides the formation of mononuclear ML species, and shows a good binding affinity for Ln3+ (log KLnL = 17.5-18.7). These complexes are also thermodynamically stable at physiological pH (pEu = 18.6, pTb = 18.0). It should be noted that the pGd value of Gd-tpptac (18.4) is only slightly lower than that of commercially available MRI contrast agents such as Gd-dota (pGd = 19.2). Moreover, a very good selectivity for these ions over the endogenous cations (log KCuL = 14.4, log KZnL = 1…

LanthanideAqueous solution010405 organic chemistrychemistry.chemical_elementTerbium010402 general chemistryLigand (biochemistry)01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographychemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryBond energyEuropiumLuminescence
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Effect of the metal dilution on the thermal and light-induced spin transition in [FexMn1−x(bpp)2](NCSe)2: When T(LIESST) reaches T1/2

2008

International audience; The thermal and light-induced spin transition in [FexMn1−x(bpp)2](NCSe)2 (bpp = 2,6-bis(pyrazol-3-yl)pyridine) has been investigated by magnetic susceptibility, photomagnetism and diffuse reflectivity measurements. These complexes display a thermal spin transition and exhibit the light-induced excited spin state trapping (LIESST) effect at low temperature. For each mixed-crystal system, the thermal spin transition temperature, T1/2, and the relaxation temperature of the photo-induced high-spin state, T(LIESST), have been systematically determined. It appears that T1/2 decreases with the metal dilution while T(LIESST) remains unchanged, suggesting that the two interco…

Ligand field theoryCondensed matter physicsSpin states010405 organic chemistryChemistryRelaxation (NMR)Spin transition[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistryPhotomagnetismSpin crossover01 natural sciencesMagnetic susceptibilityLIESST0104 chemical sciencesCoordination chemistryInorganic ChemistrySpin crossoverMaterials ChemistryPhysical chemistryPhysical and Theoretical ChemistryMetal dilutionPhotomagnetism
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Guidelines to design new spin crossover materials

2010

International audience; This review focuses on new families of spin crossover (SCO) complexes based on polynitrile anions as new anionic ligands or on polyazamacrocycles as neutral macrocyclic ligands. We have shown that the structural and electronic characteristics (original coordination modes and high electronic delocalization) of the polynitrile anions can be tuned by slight chemical modifications such as substitution of functional groups or variation of the negative charge to design new discrete or polymeric SCO systems.In our ongoing work on the design of new molecular systems based on new ligands that can be fine-tuned via chemical modifications, another promising way which has been r…

Ligand field theoryDenticityStereochemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistryMolecular systemsIron(II) complexes010402 general chemistry01 natural sciencesInorganic ChemistryMetalMacrocyclic ligandsDelocalized electronSpin crossoverNegative chargeMagnetic propertiesMaterials Chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryChemistrySpin crossover0104 chemical sciencesCoordination polymersPolynitrileCrystallographyvisual_artvisual_art.visual_art_mediumCoordination Chemistry Reviews
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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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Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, andMagnetic Properties

2015

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, MnII, FeII, CoII, or NiII, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)2] and [Fe(1)(hfac)2] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the meta…

Magnetic susceptibility measurementsAntiferromagnetic couplingIron compoundsLigands01 natural sciencesNickelheterosyklitMetal ionsta116Cobalt compoundsChelationChemistryMetal–radical interactionsMagnetismSingle crystal x-ray diffractionRadicals[CHIM.MATE]Chemical Sciences/Material chemistrymetal-radical interactionsradicalsexchange interactionsChemistrykoordinaatiokemiaUnpaired electronPositive ionsMetalsSynthesis (chemical)visual_artradikaalitvisual_art.visual_art_mediumElectronic structureCoordinating propertiesmagneettiset ominaisuudetX ray diffractionRadicalInorganic chemistryRadical interactionsElectronic structureHeterocycles010402 general chemistryCatalysisMagnetic susceptibilityMetalElectronic structure calculationsMetal complexesMagnetic properties[CHIM.COOR]Chemical Sciences/Coordination chemistrymetalli-radikaali -vuorovaikutuksetManganeseheterocycles010405 organic chemistryLigandCrystal structureOrganic ChemistryGeneral ChemistryMagnetic susceptibility0104 chemical sciencesCrystallographyOctahedronFerromagnetismExchange interactionscoordination chemistrySingle crystalsmagnetic propertiesCoordination reactions
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Magnetism and Molecular Nonlinear Optical Second-Order Response Meet in a Spin Crossover Complex

2012

International audience; The quadratic hyperpolarizability of two inorganic Schiff base metal complexes which differ from each other by the nature of the central metal ion (FeII or ZnII) is estimated using hyper-Rayleigh light-scattering (HRS) measurements. The investigated FeII microcrystals exhibit a thermal spin-crossover (SCO) from a diamagnetic to a paramagnetic state centered at T1/2 = 233 K that can be reproduced by the HRS signal whose modest intensity is mainly due to their centrosymmetric packing structure. Diamagnetic ZnII microcrystals even lead to much weaker (∼400 times) HRS intensities which are in addition temperature-independent. These observations allow us to ascribe the ch…

MagnetismHyperpolarizability02 engineering and technology010402 general chemistry01 natural sciencesMolecular physicsMetalParamagnetismchemistry.chemical_compoundNuclear magnetic resonanceSpin crossover[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistrySchiff basebusiness.industry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral Energychemistryvisual_artvisual_art.visual_art_mediumDiamagnetismPhotonics0210 nano-technologybusiness
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An {Fe60} tetrahedral cage: building nanoscopic molecular assemblies through cyanometallate and alkoxo linkers

2016

International audience; A nanoscopic {Fe60} coordination cage (approximately 3 nm) was prepared by the self assembly of a partially blocked tricyanidoferrate(III) complex and tris(alkoxo)-based iron(III) coordination motifs. This cage is a rare example of a mixed cyanido/alkoxo-bridged high nuclearity complex and it exemplifies the great potential of this new synthetic route to generate uncommon molecular architectures using cyanometallates as metalloligands versus alkoxo-based polynuclear entities.

Materials science010405 organic chemistry010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographyCoordination cageComputational chemistryTetrahedron[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryCageNanoscopic scale
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Nanocatalysts for High Selectivity Enyne Cyclization: Oxidative Surface Reorganization of Gold Sub-2-nm Nanoparticle Networks

2021

International audience; Ultrasmall gold nanoparticles (NPs) stabilized in networks by polymantane ligands (diamondoids) were successfully used as precatalysts for highly selective heterogeneous gold-catalyzed dimethyl allyl(propargyl)malonate cyclization to 5-membered conjugated diene. Such reaction usually suffers from selectivity issues with homogeneous catalysts. This control over selectivity further opened the way to one-pot cascade reaction, as illustrated by the 1,6-enyne cycloisomerization–Diels–Alder reaction of dimethyl allyl propargyl malonate with maleic anhydride. The ability to assemble nanoparticles with controllable sizes and shapes within networks concerns research in sensor…

Materials scienceAlkyneLigands010402 general chemistry01 natural sciencesArticleenyne cyclizationCycloisomerizationCascade reactionSelectivity[CHIM.COOR]Chemical Sciences/Coordination chemistryQD1-999chemistry.chemical_classificationdiamondoidsEnyne010405 organic chemistryCombinatorial chemistryHydrocarbonsNanomaterial-based catalyst0104 chemical sciencesChemistrychemistryCyclizationColloidal goldgold sub-2-nm nanoparticlesPropargylnanocatalystsGoldSelectivityJACS Au
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Porous materials applied to biomarker sensing in exhaled breath for monitoring and detecting non-invasive pathologies

2020

International audience; Overview of the use of porous materials for gas sensing to analyze the exhaled breath of patients for disease identification.The quantification of specific gases among thousand of VOCs (Volatile Organic Compounds) present in the human breath at the ppm/ppb level can be used to evidence the presence of diseases in the human body. The detection of these biomarkers in human exhaled breath through a noninvasive approach is an important field of research which is still attracting important attention to this day. A portable device working at room temperature and usable directly on exhaled breath samples is still a challenge requiring a sensing material with high performanc…

Materials scienceCrystalline materialsNon invasiveNanotechnology[CHIM.MATE]Chemical Sciences/Material chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyHighly selective01 natural sciences0104 chemical sciencesInorganic Chemistry[CHIM.POLY]Chemical Sciences/PolymersBreath TestsExhalationLimit of DetectionHighly porousHumans[CHIM.COOR]Chemical Sciences/Coordination chemistry[SDV.IB]Life Sciences [q-bio]/Bioengineering0210 nano-technologyPorous mediumPorosityBiomarkersDalton Transactions
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Magnesium(II) polyporphine: The first electron-conducting polymer with directly linked unsubstituted porphyrin units obtained by electrooxidation at …

2010

Abstract Electrooxidation of magnesium(II) porphine, a totally unsubstituted porphyrin, in acetonitrile solution under potentiostatic or potentiodynamic regime leads to a polymer film at the electrode surface. Polymer deposition takes place at extremely low potential, several hundred mV less positive even compared to the deposition potential for pyrrole or EDOT (at identical monomer concentrations) in the same solvent. Film thickness can be controlled by the passed deposition charge. This material and its THF-soluble fraction have been characterized by various electrochemical methods as well as by UV–visible and IR spectroscopies, XPS, XRD and MALDI-TOF techniques. This analysis has allowed…

Materials scienceGeneral Chemical EngineeringInorganic chemistry02 engineering and technology010402 general chemistryElectrochemistry01 natural scienceschemistry.chemical_compoundX-ray photoelectron spectroscopy[CHIM.ANAL]Chemical Sciences/Analytical chemistryElectrochemistryElectroactive polymers[CHIM.COOR]Chemical Sciences/Coordination chemistryAcetonitrileComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationConductive polymer[CHIM.ORGA]Chemical Sciences/Organic chemistryPolymer[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencesMonomerchemistry0210 nano-technology
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