Search results for "Porphyrin"

showing 10 items of 474 documents

Spectroscopic and quantum chemical study of pressure effects on solvated chlorophyll

2004

Abstract Hydrostatic pressure effects up to 907 MPa on absorption spectra of chlorophyll a molecules dissolved in diethyl ether have been studied at ambient temperature both experimentally and theoretically using quantum chemistry methods. The fluorescence spectra are studied only experimentally. The data suggest that coordination interactions between the central Mg atom of the chlorophyll and solvent molecules along with interactions that modify the porphyrin skeleton of the solute are responsible for the observed differences of pressure dependence of the Q y , Q x , and Soret spectral bands. The coordination number of the Mg atom changes from five to six between 400 and 600 MPa.

Absorption spectroscopyChemistryCoordination numberHydrostatic pressureAnalytical chemistryGeneral Physics and AstronomyPhotochemistryPorphyrinQuantum chemistrySolventchemistry.chemical_compoundAtomMoleculePhysical and Theoretical ChemistryChemical Physics Letters
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Crystallographic and (spectro)electrochemical characterizations of cobalt(II) 10-phenyl-5,15-di-p-tolylporphyrin

2021

International audience; The synthesis, cyclic and rotating disk electrode voltammograms, UV-visible absorption and Xray diffraction analyses of cobalt(II) 10-phenyl-5,15-dip -tolylporphyrin (1-Co) are described. 1-Co was crystallized by slow diffusion of n-hexane into a concentrated CH2Cl2 solution. X-ray diffraction analyses reveals porphyrin aromatic cycle stacking in the crystal, C-H•••π interactions of the CH2Cl2 solvent with the π-system of one tolyl group and Co(II)•••π (porphyrin ring) interactions. The abstraction of 1.0 F/mol during the electrolysis at the first oxidation potential was followed by spectroelectrochemistry. It leads to the Co(II) → Co(III) transformation rather than …

Absorption spectroscopyStackingchemistry.chemical_elementCo(II)•••pi interactions010402 general chemistryElectrochemistryElectrosynthesis01 natural sciencesAnalytical Chemistrylaw.inventionInorganic ChemistryPorphyrinchemistry.chemical_compoundlaw[CHIM.ANAL]Chemical Sciences/Analytical chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryRotating disk electrodeSpectroscopyX-ray crystallographic structureElectrolysis010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryCobalt[CHIM.MATE]Chemical Sciences/Material chemistryPorphyrin0104 chemical sciencesCrystallographychemistrystacked aromatics dimersElectrosynthesisC-H•••pi interactionsCobalt
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Synthesis, Characterization, and Electrochemistry of Open-Chain Pentapyrroles and Sapphyrins with Highly Electron-Withdrawing meso -Tetraaryl Substit…

2017

International audience; A series of open-chain pentapyrroles and sapphyrins with highly electron-withdrawing substituents (i.e., CN, CF3 , or CO2 Me) on the meso-phenyl rings was synthesized and characterized as to the spectral properties, protonation reactions, and electrochemistry in non-aqueous media. The investigated compounds are represented as (Ar)4 PPyH3 and (Ar)4 SapH3 where PPy and Sap correspond to the tri-anion of the open-chain pentapyrrole and sapphyrin, respectively, and Ar=p-CNPh, p-CF3 Ph, or p-CO2 MePh. UV/Vis and 1 H NMR spectroscopy as well as mass spectrometry data are given for the confirmation of the structures for the newly synthesized compounds. An X-ray structure fo…

Absorption spectroscopyprotonationInorganic chemistryporphyrinoidsProtonationpentapyrroles010402 general chemistry01 natural sciencesRedox[ CHIM ] Chemical SciencesCatalysischemistry.chemical_compound[SPI]Engineering Sciences [physics]PyridinePolymer chemistryTrifluoroacetic acid[CHIM]Chemical SciencesEquilibrium constantsapphyrins010405 organic chemistryOrganic ChemistryGeneral Chemistry0104 chemical scienceschemistryelectrochemistryProton NMRCyclic voltammetry
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Photodynamic therapy of nodular basal cell carcinoma with multifiber contact light delivery.

2006

To overcome the limited treatment depth of superficial photodynamic therapy we investigate interstitial light delivery. In the present work the treatment light was delivered using a system in which three or six clear-cut fibers were placed in direct contact with the tumor area. This placement was thought to represent a step toward general purpose interstitial PDT. Twelve nodular basal cell carcinomas were treated employing delta-aminolevulinic acid and 635 nm laser irradiation. Fluorescence measurements were performed monitoring the buildup and subsequent bleaching of the produced sensitizer protoporphyrin IX. The treatment efficacy, judged at a 28-month follow-up, showed a 100% complete re…

AdultMalePathologymedicine.medical_specialtySkin NeoplasmsHealth Toxicology and Mutagenesismedicine.medical_treatmentNodular basal cell carcinomaProtoporphyrinsPhotodynamic therapyToxicologyLight deliveryFluorescencePathology and Forensic Medicinechemistry.chemical_compoundCarcinomamedicineHumansComplete responseAgedPhotosensitizing AgentsProtoporphyrin IXbusiness.industryLasersGeneral MedicineAminolevulinic AcidMiddle Agedmedicine.diseaseTreatment efficacyGeneral purposechemistryPhotochemotherapyCarcinoma Basal CellFemalebusinessNuclear medicineJournal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer
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Photodynamic therapy with verteporfin for subfoveal choroidal neovascularization secondary to pathologic myopia: long-term study.

2006

Purpose: To assess the safety and effectiveness of photodynamic therapy (PDT) with verteporfin for subfoveal choroidal neovascularization (CNV) secondary to pathologic myopia (PM). Methods: Sixty-two patients (62 eyes) with PM underwent PDT according to the guidelines of the Verteporfin in Photodynamic Therapy Study. Clinical evaluations performed at all study visits included measurement of best-corrected Snellen visual acuity, slit-lamp biomicroscopy, and fundus fluorescein angiography. Patients were followed up at 1 month and 3 months after treatment and thereafter at 3-month intervals. Results: The final visual acuity of the study patients, after a median follow-up of 31 months, improved…

AdultMaleRefractive errormedicine.medical_specialtyFovea CentralisVisual acuityPorphyrinsgenetic structuresmedicine.medical_treatmentVisual AcuityPhotodynamic therapyOphthalmologyPathologic myopiamedicineHumansProspective StudiesFluorescein AngiographyDioptreAgedAged 80 and overPhotosensitizing Agentsbusiness.industryVerteporfinGeneral MedicineMiddle Agedmedicine.diseaseVerteporfineye diseasesChoroidal NeovascularizationOphthalmologyLong term learningChoroidal neovascularizationPhotochemotherapyMyopia DegenerativeFemalesense organsmedicine.symptombusinessmyopia subfoveal choroidal neovascularization photodynamic therapy verteporfin.medicine.drugFollow-Up StudiesRetina (Philadelphia, Pa.)
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Photodynamic therapy with verteporfin for juxtafoveal choroidal neovascularization in pathologic myopia: a long-term follow-up study.

2007

Purpose To assess the effect of verteporfin photodynamic therapy (PDT) in juxtafoveal choroidal neovascularization (CNV) secondary to pathologic myopia (PM). Design Prospective, open-label, consecutive, interventional case series. Methods We prospectively followed a series of 48 consecutive patients (49 eyes) with pathologic myopia (≥ 6 diopters) who received verteporfin PDT for juxtafoveal CNV. This population was divided into two groups based on age (group A ≤ 55 years old, group B >55 years old), in three subgroups based on CNV lesion size, and in three categories based on refractive error at baseline. Results The median follow-up was 32 months (range, 12 to 56 months). Visual acuity (VA…

AdultMalemedicine.medical_specialtyRefractive errorFovea CentralisVisual acuityPorphyrinsgenetic structuresEye diseasePopulationVisual AcuityVision disorderlavoro clinico con dati originaliOphthalmologymedicineHumansProspective StudiesFluorescein AngiographyeducationDioptreAgedAged 80 and overeducation.field_of_studyPhotosensitizing Agentsbusiness.industryVerteporfinMiddle Agedmedicine.diseasePrognosisVerteporfineye diseasesChoroidal NeovascularizationOphthalmologyChoroidal neovascularizationPhotochemotherapyMyopia DegenerativeFemalesense organsmedicine.symptombusinessmedicine.drugFollow-Up StudiesAmerican journal of ophthalmology
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Theoretical characterization of iron and manganese porphyrins for catalyzed saturated alkane hydroxylations

1997

Abstract The theoretical characterization of porphin (H2Por), iron and manganese porphyrins MIII(Por) and their chlorine derivatives MIII(Por)Cl has been carried out. This work represents a first step for modelling catalyzed saturated alkane hydroxylations. The chlorine atom is responsible for the existence of a dipole moment of 1.2–2.0 D in the MIII(Por)Cl molecules and for a negative value of the mean quadrupole moment (−16–(−14)DA). The charge of the metal atom (1.8–2.2 e) is rather varied (to 2.1–2.6 e) and the effective polarizability (2.8–2.9 A3) is increased (to 3.5–3.6 A3) by the addition of the chlorine atom. Starting from the porphin molecule, the presence of the metal atom decrea…

Alkanechemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementManganesePorphyrinCatalysisAccessible surface areaMetalchemistry.chemical_compoundchemistryPolarizabilityvisual_artpolycyclic compoundsvisual_art.visual_art_mediumPhysical chemistryMoleculePhysical and Theoretical ChemistryPorphinJournal of Molecular Catalysis A: Chemical
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Evidence of tetraphenylporphyrin monoacids by ion-transfer voltammetry at polarized liquid|liquid interfaces

2008

We present a simple methodology to illustrate the existence of tetraphenylporphyrin monoacid based on ion-transfer voltammetry at a polarized water|1,2-dichloroethane interface and organic pK values are also estimated.

Analytical chemistry02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compound[ CHIM.OTHE ] Chemical Sciences/OtherTetraphenylporphyrinMaterials ChemistryLiquid liquidliquid-liquid interfaceion-transfer voltammetryVoltammetryComputingMilieux_MISCELLANEOUSMetals and AlloysGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesIon transfer[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyporphyrinChemical Communications
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Soret emission from water-soluble porphyrin thin films: effect on the electroluminescence response

2009

The emission properties of TSPP [tetrakis(4-sulfonatophenyl) porphyrin] and TMPyP [tetrakis(4-methylpyridyl) porphyrin] in thin films, prepared both by the Langmuir–Blodgett technique and the spin-coating method, have been investigated. Surprisingly, in most of the samples analyzed, the emission spectra do not show the usual two bands typical of porphyrins (in the region 650–750 nm), and depend strongly on the excitation energy. The origin of a new emission band detected at ∼480–500 nm is discussed in terms of the nature of the porphyrin aggregates. Moreover, we demonstrate that the presence or absence of this band in the fluorescence spectrum is directly related to the generation of electr…

Analytical chemistryGeneral ChemistryElectroluminescencePhotochemistryFluorescencePorphyrinlaw.inventionchemistry.chemical_compoundchemistrylawMaterials ChemistryOLEDEmission spectrumThin filmLuminescenceLight-emitting diodeJournal of Materials Chemistry
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Recent advances in electrochemical meso- and β-functionalization of porphyrins and electrografting of diazonium porphyrins

2020

Abstract Recent studies on electrochemical meso- and β-functionalization of porphyrins and electrografting of diazonium porphyrin are presented. First, the electrochemical oxidative C–C coupling between porphyrins will be presented, followed by the intermolecular and intramolecular meso- and β-substitutions of porphyrins. Then, the latest results on diazonium porphyrin electrografting will be reviewed.

Anodic nucleophilic substitution02 engineering and technology010402 general chemistryPhotochemistryElectrochemistry01 natural sciencesDiazonium-porphyrin electrograftingAnalytical ChemistryPorphyrinchemistry.chemical_compoundOrganic electrosynthesis[CHIM.ANAL]Chemical Sciences/Analytical chemistryElectrochemistry[CHIM.COOR]Chemical Sciences/Coordination chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryIntermolecular forceElectropolymerization[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencesCoupling (electronics)chemistryIntramolecular forceSurface modification0210 nano-technology
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