Search results for "COORDINATION CHEMISTRY"

showing 10 items of 231 documents

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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Modulating the Electrical Properties of Organic Heterojunction Devices Based On Phthalocyanines for Ambipolar Sensors.

2020

International audience; HAL is a multidisciplinary open access archive for the deposit and dissemination of scientific research documents, whether they are published or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers. L'archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d'enseignement et de recherche français ou étrangers, des laboratoires publics ou privés.

Materials scienceIndolesBioengineering02 engineering and technologyIsoindoles01 natural sciencesMolecular semiconductor[CHIM.ANAL]Chemical Sciences/Analytical chemistryAmmonia[CHIM.COOR]Chemical Sciences/Coordination chemistryMolecular materialsInstrumentationFluid Flow and Transfer ProcessesOrganic electronicsAmbipolar diffusionbusiness.industryProcess Chemistry and TechnologyBilayer010401 analytical chemistryWaterHeterojunctionHumidity021001 nanoscience & nanotechnology0104 chemical sciencesOptoelectronics0210 nano-technologybusinessACS sensors
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BODIPY–diketopyrrolopyrrole–porphyrin conjugate small molecules for use in bulk heterojunction solar cells

2018

Two small molecules denoted as BD-pPor and BD-tPor composed of a central BODIPY core surrounded with two DPP and two porphyrin units have been designed and synthesized. In BD-pPor and BD-tPor, porphyrins are linked to the central BODIPY by phenyl and thiophene bridges, respectively. The optical and electrochemical properties were systematically investigated in order to employ them as donors along with PC71BM as an acceptor for solution processed bulk heterojunction organic solar cells. After the optimization of the active layer, the organic solar cells based on BD-pPor and BD-tPor exhibit overall power conversion efficiencies of 6.67% and 8.98% with an energy loss of 0.63 eV and 0.50 eV. Th…

Materials scienceOrganic solar cell02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesPolymer solar cellchemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiopheneGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistryHOMO/LUMOComputingMilieux_MISCELLANEOUSRenewable Energy Sustainability and the Environment[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologySmall moleculeAcceptorPorphyrin0104 chemical scienceschemistryBODIPY0210 nano-technology
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Near-infrared photochemistry assisted by upconverting nanoparticles

2019

Abstract Upconverting nanoparticles (UCNPs) combine unique optical and imaging properties with high chemical and biological stability. The capability of UCNPs to emit visible light upon near-infrared light excitation, in an anti-Stokes fashion, is extremely attractive for the design of light-responsive nanomaterials whose action can be controlled spatially and temporally. In this chapter, we analyze the most promising approaches developed so far to functionalize the surface of UCNPs with photoactivatable organic and inorganic molecular systems. In particular, we emphasize the key advances in the design of upconverting nanosystems that exploit bioactive transition metal complexes.

Materials sciencePhotochemistryNear infraredNear-infrared spectroscopyOrganic chemistryNanotechnologyMolecular systemsCoordination chemistryNanomaterialsPhotochemotherapySettore CHIM/03 - Chimica Generale E InorganicaUpconverting nanoparticlesLanthanidesProdrugsLight excitationUpconverting nanoparticlesVisible spectrum
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Pressure effect investigations on spin-crossover coordination compounds

2018

International audience; The piezochromic properties of spin-crossover complexes have been recognized for a long time, with increasing pressure favouring the low spin state due to its smaller volume and therefore shifting the spin equilibrium towards higher temperatures and accelerating the relaxation at a given temperature. However, the interpretation and quantification of pressure-induced changes have been several times compromised by the relatively poor and incomplete spectral and structural information provided by the detection methods or due to the experimental difficulties related to the need for hydrostatic conditions at low temperatures. The present review is therefore primarily focu…

Materials scienceSpin statesGeneral Chemical Engineering02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionCoordination complexlawSpin crossoverQD[CHIM.COOR]Chemical Sciences/Coordination chemistryHigh-pressure chemistrySpin-½chemistry.chemical_classificationRelaxation (NMR)General Chemistry021001 nanoscience & nanotechnologySpin crossover0104 chemical sciencesVolume (thermodynamics)chemistryChemical physicsHydrostatic equilibrium0210 nano-technologyPressure generation
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Spin Crossover Metal-Organic Frameworks with Inserted Photoactive Guests: On the Quest to Control the Spin State by Photoisomerization

2021

International audience; Three Hofmann-like metal-organic frameworks {Fe(bpac)[Pt(CN)4]}•G (bpac=1,2-bis(4-pyridyl)acetylene) were synthesized with photoisomerizable guest molecules (G = trans-azobenzene, trans-stilbene or cis-stilbene) and were characterized by elemental analysis, thermogravimetry and powder X-ray diffraction. The insertion of guest molecules and their conformation were inferred from Raman and FTIR spectra and from single-crystal X-ray diffraction and confronted with computational simulation. The magnetic and photomagnetic behaviors of the framework are significantly altered by the different guest molecules and different conformations. On the other hand, photoisomerization …

Materials scienceSpin statesPhotoisomerization02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic ChemistryThermogravimetryCrystallographychemistry.chemical_compoundsymbols.namesakeAcetylenechemistrySpin crossoversymbols[CHIM.CRIS]Chemical Sciences/CristallographyMoleculeMetal-organic framework[CHIM.COOR]Chemical Sciences/Coordination chemistry0210 nano-technologyRaman spectroscopy
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Assignment of complex species by affinity capillary electrophoresis: The case of Th(IV)‐desferrioxamine B

2020

International audience; The electrophoretic mobility change of desferrioxamine B (DFO) was monitored by UV absorption spectrophotometry upon increasing the thorium(IV) concentration in the background electrolyte at two acidities ([HClO4]Tot = 0.0316 and 0.0100 M). These data enabled to assess the speciation model and to determine the equilibrium constant of [Th(DFO)H2]3+ at fixed ionic strength (I = 0.1 M (H,Na)ClO4). Affinity capillary electrophoresis (ACE) turned out to be most helpful in identifying the complexed species by ascertaining its charge and protonation state. The assignment of the correct stoichiometry relied on the reliable estimation of the electrophoretic mobility by assumi…

Metal ions in aqueous solutionClinical BiochemistryProtonation02 engineering and technologyDeferoxamine01 natural sciencesBiochemistryDFTAnalytical ChemistryCapillary electrophoresisAffinity capillary electrophoresis[CHIM.ANAL]Chemical Sciences/Analytical chemistrySpectrophotometrymedicine[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryStability constantsEquilibrium constantDensity Functional Theorymedicine.diagnostic_testChemistryLigand010401 analytical chemistryThoriumElectrophoresis Capillary021001 nanoscience & nanotechnology0104 chemical sciencesElectrophoresisDesferrioxamine BIonic strengthPhysical chemistrySpectrophotometry UltravioletComplexation0210 nano-technology
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Photophysical properties of a rhodium tetraphenylporphyrin-tin corrole dyad. The first example of a through metal-metal bond energy transfer

2005

The luminescence spectroscopy study and the determination of the photophysical parameters for the M-M'-bonded rhodium meso-tetraphenylporphyrin-tin(2,3,7,13,17,18-hexamethyl-8,12-diethylcorrole) complex, (TPP)Rh-Sn(Me6Et2Cor) 1, was investigated. The emission bands as well as the lifetimes (tau(e)) and the quantum yields (Phi(e); at 77 K using 2MeTHF as solvent) were compared with those of (TPP)RhI 2 (TPP = tetraphenylporphyrin) and (Me6Et2Cor)SnCl 3 (Me6Et2Cor = 2,3,7,13,17,18-hexamethyl-8,12-diethylcorrole) which are the two chemical precursors of 1. The energy diagram has been established from the absorption, fluorescence and phosphorescence spectra. The Rh(TPP) and Sn(Me6Et2Cor) chromop…

MetalloporphyrinsPhotochemistrychemistry.chemical_element010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesBiochemistryRhodiumchemistry.chemical_compoundrhodium porphyrinTetraphenylporphyrinRhodium[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryBond energyCorrole010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryGeneral MedicineAcceptor3. Good health0104 chemical sciencesEnergy TransferchemistryMetalsSpectrophotometryExcited statemetal-metal bond energy transferTinPhosphorescencetin corrole
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New concepts in multidentate ligand chemistry: effects of multidentarity on catalytic and spectroscopic properties of ferrocenyl polyphosphines.

2008

This tutorial review devoted to ligand chemistry deals with the design and properties of ferrocenyl polyphosphines, an original class of multidentate ligands. The development of a varied library of ferrocenyl tetra-, tri- and diphosphine ligands is reviewed. The multidentate nature of these species has led to unique spectroscopic and catalytic properties, in which the spatial proximity of phosphorus atoms is crucial. Regarding their catalytic applications, the key issues of catalyst longevity and ultralow catalyst loadings are discussed. Another part is concerned with fundamental advances gained in physical chemistry for structure elucidation by the study of the intriguing “through-space” N…

Models MolecularDenticityMagnetic Resonance SpectroscopyMetallocenesferrocenyl polyphosphinesSuzukiMolecular ConformationSonogashira coupling010402 general chemistryLigands01 natural sciencescatalystsCatalysisCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysisthrough-space interactionOrganometallic CompoundsOrganic chemistryCombinatorial Chemistry Techniques[CHIM.COOR]Chemical Sciences/Coordination chemistryFerrous CompoundsAminationComputingMilieux_MISCELLANEOUSGroup 2 organometallic chemistryCombinatorial Chemistry Techniquesnuclear spin-spin coupling010405 organic chemistryChemistryLigand[ CHIM.COOR ] Chemical Sciences/Coordination chemistrySonogashiraaminationStereoisomerismGeneral ChemistryNuclear magnetic resonance spectroscopy[CHIM.CATA]Chemical Sciences/CatalysisReference StandardsCombinatorial chemistry0104 chemical sciencesmultidentarityHeckChemical Society reviews
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DOTAGA-Trastuzumab. A New Antibody Conjugate Targeting HER2/Neu Antigen for Diagnostic Purposes.

2012

International audience; Improved bifunctional chelating agents (BFC) are required for indium-111 radiolabeling of monoclonal antibodies (mAbs) under mild conditions to yield stable, target-specific agents. 2,2',2″-(10-(2,6-Dioxotetrahydro-2H-pyran-3-yl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetic acid (DOTAGA-anhydride) was evaluated for mAb conjugation and labeling with indium-111. The DOTA analogue was synthesized and conjugated to trastuzumab-which targets the HER2/neu receptor-in mild conditions (PBS pH 7.4, 25 °C, 30 min) and gave a mean degree of conjugation of 2.6 macrocycle per antibody. Labeling of this immunoconjugate with indium-111 was performed in 75% yield after 1 h a…

Models MolecularImmunoconjugatesReceptor ErbB-2Pharmaceutical Science[CHIM.THER]Chemical Sciences/Medicinal Chemistry[ SDV.CAN ] Life Sciences [q-bio]/CancerMicechemistry.chemical_compound0302 clinical medicineTrastuzumabBreastMice Inbred BALB C0303 health sciencesbiologyChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryIndium Radioisotopes[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.THER ] Chemical Sciences/Medicinal Chemistry3. Good healthBiochemistry030220 oncology & carcinogenesisMonoclonalFemaleAntibody[CHIM.RADIO]Chemical Sciences/Radiochemistry[ CHIM.RADIO ] Chemical Sciences/RadiochemistryBiotechnologymedicine.drugBiodistributionmedicine.drug_classBiomedical EngineeringBreast NeoplasmsBioengineering[SDV.CAN]Life Sciences [q-bio]/CancerAntibodies Monoclonal HumanizedMonoclonal antibodyAnhydridesHeterocyclic Compounds 1-Ring03 medical and health sciences[ CHIM.ORGA ] Chemical Sciences/Organic chemistryCell Line TumormedicineAnimalsHumansDOTA[CHIM.COOR]Chemical Sciences/Coordination chemistry030304 developmental biologyTomography Emission-Computed Single-PhotonPharmacologyOrganic ChemistryTrastuzumabMolecular biologyIn vitroImmunoconjugatebiology.protein
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