Search results for " porphyrin"

showing 10 items of 31 documents

Towards the synthesis of substituted porphyrins by a pyridyl group bearing a reactive functionality

2010

Pyridyl-substituted porphyrins bearing a reactive functionality were prepared via Suzuki cross-coupling reactions and resulted in very good yields. These compounds are precursors of new porphyrin architectures able to coordinate two metals: one in the porphyrin core and the second around the pyridyl moiety. During the coupling reactions, a higher reactivity of a chloro picolyl group was evidenced compared to a bromo function on the same reacting molecule.

010405 organic chemistryChemistryStereochemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry010402 general chemistry01 natural sciencesPorphyrinCoupling reaction0104 chemical sciencesA3B-porphyrinschemistry.chemical_compoundSuzuki reactionGroup (periodic table)[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPolymer chemistrypolycyclic compoundsMoietyMoleculeheterocyclic compoundsReactivity (chemistry)meso-functionalizationSuzuki couplingpyridyl substituted porphyrinsComputingMilieux_MISCELLANEOUS
researchProduct

Contributory presentations/posters

1999

0303 health sciencesbiologyGeneral Medicine010402 general chemistry01 natural sciencesHorseradish peroxidaseGeneral Biochemistry Genetics and Molecular Biology0104 chemical sciences03 medical and health sciencesBiochemistryManganese porphyrinbiology.proteinEnzyme reconstitutionGeneral Agricultural and Biological Sciences030304 developmental biologyJournal of Biosciences
researchProduct

Inter- and Intramolecular Anodic Nucleophilic Substitutions of Porphyrins. Reactivity of the resulting products

2020

This manuscript presents the functionalization of porphyrins by anodic nucleophilic substitution (SNAn). After an introduction describing generalities on porphyrin, the 2nd chapter deals with the 2-step synthesis of primary aminoporphyrins. The 1st electrochemical step consists in oxidizing the porphyrin at the 1st oxidation potential in the presence of pyridine. The formed pyridinium-porphyrin is then transformed into an amine by opening the pyridinium fragment by nucleophilic attack of piperidine.The 3rd chapter presents the synthesis and redox reactivity of porphyrins substituted with one (or several) aromatic groups carrying an imine function (thiopyrimidine, quinoline and aminopyridine…

C-N FusionPorphyrinsAminoporphyrinPorphyrineSubstitution Nucléophile AnodiqueAminoporphyrine[CHIM.OTHE] Chemical Sciences/OtherFusion C-NNucléophilic Anodic SubstitutionFerrocenylporphyrinFerrocénylporphyrinePyrifinium-PorphyrinPyridinium- porphyrine
researchProduct

New insights on the electronic, magnetic, electric and molecular structure of a bis-(4-cyanopyridine) iron(III) complex with the meso-tetrakis(4-meth…

2019

International audience; We have successfully synthesized and characterized a new low-spin iron(III) bis(4-cyanopyridine) complex with a meso-porphyrin substituted in the para positions of the phenyls by the methoxy group, namely the bis(4-cyanopyridine)[(meso-tetrakis(4-metoxyphenylporphyrinato)]iron(III) trifluoromethanesulfonate chlorobenzene monosolvate complex with the formula [FeIII(TMPP)(4-CNpy)2]SO3CF3.C6H5Cl (I). This species was characterized through ultraviolet–visible, Fourier-transform infrared and Mössbauer spectroscopy as well as by SQUID magnetometry, cyclic voltammetry, and X-ray crystallography. These characterizations indicated that our synthetic heme model is a low-spin (…

Cyclic voltammetryInfrared010402 general chemistry01 natural sciencesCoordination complexInorganic Chemistrychemistry.chemical_compoundMagnetic propertiesMössbauer spectroscopy[CHIM.CRIS]Chemical Sciences/CristallographyMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryX-ray Molecular structureHemechemistry.chemical_classification010405 organic chemistryChemistryIron(III) porphyrin0104 chemical sciences3. Good healthCrystallographyChlorobenzeneCyclic voltammetryTrifluoromethanesulfonateInorganica Chimica Acta
researchProduct

Synthesis, spectroscopic, cyclic voltammetry properties and molecular structure of the thiocyanato-N meso-tetratolylporphyrinato zinc(II) ion complex

2017

International audience; This paper describes the synthesis of the (thiocyanato-N)(meso-tetratolylporphyrinato)zinc(II) chlorobenzene monosolvate complex with the formula [K(2,2,2-crypt)][Zn(TTP)(NCS)]·C6H5Cl (I) using the cryptand-222 to solubilize potassium thiocyanate in chlorobenzene solvent. Complex (I) has been characterized by elementary analysis, IR, UV–vis, 1H NMR and MS, and the structure of this new zinc(II) metalloporphyrin been examined crystallographically. A cyclic voltammetry investigation was also carried out on this species. The title compound crystallizes in the triclinic, space group P-1, with a = 11.5151(7) Å, b = 15.212(10) Å, c = 20.1093(12) Å, α = 80.428(4)°, β = 74.9…

Cyclic voltammetryInorganic chemistrychemistry.chemical_elementZincTriclinic crystal system010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciences[ CHIM ] Chemical SciencesAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundPotassium thiocyanateUV–visible[CHIM]Chemical SciencesSpectroscopyOrganic ChemistryPorphyrinZinc porphyrin complex0104 chemical sciences3. Good healthX-ray diffractionCrystallographychemistryChlorobenzeneX-ray crystallographyProton NMRCyclic voltammetry
researchProduct

Electroactive polymeric material with condensed structure on the basis of magnesium(II) polyporphine

2011

International audience; Previous publication of the authors presented evidences that electroch emical oxidation of Mg(II) porphine (fully unsubstituted porphyrin, MgP) in acetonitrile (AN) at a very low potential leads to deposition of films at electrode surface corresponding to typical electroactive polymers, with their reversible transition betwee n the electronconducting and insulating states depending on the electrode potential/oxidation level ("film of type I"). It is demonstrated in the actual publication that these films in contact with a monomer-free solution are subject to an irreversible transformation to quite a different material ("film of type II") under the influence of a high…

General Chemical EngineeringAnalytical chemistryInfrared spectroscopy02 engineering and technology010402 general chemistryElectrochemistry01 natural scienceschemistry.chemical_compoundTransition metalX-ray photoelectron spectroscopy[CHIM.ANAL]Chemical Sciences/Analytical chemistryelectroactive materialsElectrochemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryconducting polymermagnesium porphineConductive polymer[CHIM.ORGA]Chemical Sciences/Organic chemistryelectropolymerization[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMonomerchemistryPhysical chemistryC-C coupling0210 nano-technologyunsubstituted porphyrinElectrode potentialElectrochimica Acta
researchProduct

Photo-induced electron transfer at nanostructured semiconductor–zinc porphyrin interface

2014

Abstract Electron transfer at metal oxide–organic dye interface on ZnO nanorod (ZnOr) templates was studied by femtosecond absorption spectroscopy method. Further confirmation of the electron transfer was obtained from photoelectrical studies. The fastest electron transfer from zinc porphyrin (ZnP) to semiconductor was observed for ZnOr modified by a 5 nm layer of TiO2 (

Materials scienceAbsorption spectroscopybusiness.industryGeneral Physics and AstronomyPhotochemistryMetalZinc porphyrinElectron transferSemiconductorvisual_artFemtosecondvisual_art.visual_art_mediumNanorodPhysical and Theoretical Chemistrybusinessta116Layer (electronics)Chemical Physics Letters
researchProduct

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
researchProduct

Structural and Molecular Characterization of meso-Substituted Zinc Porphyrins: A DFT Supported Study

2011

Structural parameters of a range of over 100 meso-substituted zinc porphyrins were reviewed and compared to show how far the nature of the functional group may affect the interatomic distances and bond angles within the porphyrin core. It was proved that even despite evident deformations of the molecular structure, involving twisting of the porphyrin's central plane, the coupled π-bonding system remains flexible and stable. DFT calculations were applied to a number of selected porphyrins representative for the reviewed compounds to emphasize the relevance of theoretical methods in structural investigations of complex macrocyclic molecular systems. Experimental and DFT-simulated IR spectral …

Models Molecularzinc porphyrins; molecular structure; DFT theoretical calculations; IR spectraPorphyrinsSpectrophotometry InfraredStereochemistrySurface PropertiesPharmaceutical Sciencechemistry.chemical_elementInfrared spectroscopyContext (language use)molecular structureZincCrystallography X-RayVibrationArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundDFT theoretical calculationslcsh:Organic chemistryComputational chemistryDrug Discoveryzinc porphyrins molecular structure DFT theoretical calculations IR spectraSpectroscopy Fourier Transform InfraredMoleculeMoietyComputer SimulationPyrrolesPhysical and Theoretical ChemistryIR spectraOrganic ChemistryPorphyrinzinc porphyrinsZincMolecular geometrychemistryModels ChemicalChemistry (miscellaneous)Functional groupMicroscopy Electron ScanningMolecular MedicineQuantum TheoryMolecules
researchProduct

Covalently Conjugated Gold-Porphyrin Nanostructures

2020

Gold nanoparticles show important electronic and optical properties, owing to their size, shape, and electronic structures. Indeed, gold nanoparticles containing no more than 30&ndash

NanostructureMaterials sciencegold nanoparticle; luminescence; nanostructures; porphyrin; surface plasmon resonanceGeneral Chemical EngineeringNanoparticleNanotechnologyCovalently Conjugated Gold–Porphyrin NanostructuresArticlelcsh:Chemistrychemistry.chemical_compoundnanostructuresluminescenceGeneral Materials ScienceSurface plasmon resonancePlasmonSurface plasmonAu NPsPorphyrinlcsh:QD1-999chemistryColloidal goldgold nanoparticle luminescence nanostructures porphyrin surface plasmon resonanceLuminescenceporphyringold nanoparticlesurface plasmon resonance
researchProduct