Search results for "Photochemical Processes"

showing 10 items of 50 documents

Pyrrolo[3,4-h]quinolinones a new class of photochemotherapeutic agents

2011

Abstract Pyrrolo[3,4- h ]quinolin-2-ones were synthesized as nitrogen isosters of the angular furocoumarin angelicin, with the aim of obtaining new photochemotherapeutic agents with increased antiproliferative activity and lower undesired toxic effects. A versatile synthetic pathway was approached to allow the isolation of derivatives of the new ring system with a good substitution pattern on the pyrrole moiety. Photobiological screenings of the new compounds revealed a potent phototoxic effect and a great UVA dose dependence, reaching IC 50 values at submicromolar level. The induced cellular photocytotoxicity was related to apoptosis with the involvement of mitochondria and lysosomes, alte…

Pyrrolo[3; 4-h]quinolinones; Angelicin heteroanalogues; Photochemotherapeutic agents; PhototoxicityStereochemistryClinical BiochemistryMembrane lipid peroxidationPharmaceutical ScienceHL-60 CellsPhosphatidylserinesQuinolonesMitochondrionBiochemistryPhototoxicityJurkat CellsStructure-Activity Relationshipchemistry.chemical_compoundPhotochemotherapeutic agentsAngelicinCell Line TumorDrug DiscoveryHumansMoietyFluorometryPyrrolesPyrrolo[3Molecular BiologyPyrrolePyrrolo[34-h]quinolinoneFurocoumarinCell CycleOrganic Chemistry4-h]quinolinonesDNAPhotochemical ProcessesSettore CHIM/08 - Chimica FarmaceuticaAngelicin heteroanaloguesPhotochemotherapeutic agentPhotochemotherapychemistryApoptosisMolecular MedicineLipid PeroxidationPhototoxicityAngelicin heteroanalogueSubcellular FractionsBioorganic & Medicinal Chemistry
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Proton Transfer and Protein Conformation Dynamics in Photosensitive Proteins by Time-resolved Step-scan Fourier-transform Infrared Spectroscopy

2014

Monitoring the dynamics of protonation and protein backbone conformation changes during the function of a protein is an essential step towards understanding its mechanism. Protonation and conformational changes affect the vibration pattern of amino acid side chains and of the peptide bond, respectively, both of which can be probed by infrared (IR) difference spectroscopy. For proteins whose function can be repetitively and reproducibly triggered by light, it is possible to obtain infrared difference spectra with (sub)microsecond resolution over a broad spectral range using the step-scan Fourier transform infrared technique. With -10(2)-10(3) repetitions of the photoreaction, the minimum num…

RhodopsinMaterials scienceproton transferProtein ConformationGeneral Chemical EngineeringBiophysicsAnalytical chemistryInfrared spectroscopymembrane proteinsProtonationtime-resolved spectroscopyGeneral Biochemistry Genetics and Molecular Biologychannelrhodopsinattenuated total reflectionProtein structureSpectroscopy Fourier Transform InfraredFourier transform infrared spectroscopyinfrared spectroscopySpectroscopyIssue 88biologyGeneral Immunology and MicrobiologybacteriorhodopsinGeneral Neurosciencesingular value decompositionstep-scanProteinsEspectroscòpia infrarojaBacteriorhodopsinPhotochemical ProcessesBacteriorhodopsinsAttenuated total reflectionprotein dynamicsbiology.proteinProtonsTime-resolved spectroscopyProteïnesJournal of Visualized Experiments
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Photocrosslinkable polyaspartamide/polylactide copolymer and its porous scaffolds for chondrocytes

2017

With the aim to produce, by a simple and reproducible technique, porous scaffolds potentially employable for tissue engineering purposes, in this work, we have synthesized a methacrylate (MA) copolymer of α,β-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA) and polylactic acid (PLA). PHEA-PLA-MA has been dissolved in organic solvent at different concentrations in the presence of NaCl particles with different granulometry, and through UV irradiation and further salt leaching technique, various porous scaffolds have been prepared. Obtained samples have been characterized by scanning electron microscopy and their porosity has been evaluated as well as their degradation profile in aqueous medium in…

ScaffoldMaterials scienceSwineScanning electron microscopePolyestersBioengineering02 engineering and technology010402 general chemistryMethacrylate01 natural sciencesCartilage regeneration; Photocrosslinking; Porous scaffolds; αβ-poly(N-2-hydroxyethyl)-DL-aspartamideBiomaterialschemistry.chemical_compoundChondrocytesPorous scaffoldTissue engineeringPolylactic acidPolymer chemistryCopolymerAnimalsPorosityPhotocrosslinkingαβ-poly(N-2-hydroxyethyl)-DL-aspartamideTissue EngineeringTissue Scaffoldstechnology industry and agriculturePhotochemical Processes021001 nanoscience & nanotechnology0104 chemical sciencesCross-Linking ReagentschemistryChemical engineeringCartilage regenerationSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoMechanics of MaterialsCattleLeaching (metallurgy)0210 nano-technologyPorosityMaterials Science and Engineering: C
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Green Oxidation of Alcohols to Carbonyl Compounds by Heterogeneous Photocatalysis

2010

TitaniumAldehydesChemistryGeneral Chemical EngineeringKetonesHeterogeneous catalysisPhotochemistryPhotochemical ProcessesSilicon DioxideCatalysisGeneral EnergyAlcohol oxidationAlcoholsAlcohols Chemoselectivity Heterogeneous Catalysis Oxidation PhotocatalysisPhotocatalysisEnvironmental ChemistryOrganic chemistryGeneral Materials ScienceChemoselectivityOxidation-ReductionEnvironmental Restoration and Remediation
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Hydrothermal Synthesis of Ionic Liquid [Bmim]OH-Modified TiO2 Nanoparticles with Enhanced Photocatalytic Activity under Visible Light

2010

TiO(2) nanocomposites modified with the ionic liquid [Bmim]OH are synthesized by a hydrothermal procedure. X-ray diffraction, Zeta-potential measurement, TEM, thermogravimetric analysis, photoluminescence, UV/Vis, FTIR, and X-ray photoelectron spectroscopy are used to characterize the TiO(2) nanocomposites. The TiO(2) nanocomposites consist of pure anatase particles of about 10 nm. The modification of [Bmim]OH on the surface of the TiO(2) particles extends the TiO(2) absorption edge to the visible-light region. The electrochemical redox potentials indicated that the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of [Bmim]OH match well with the valen…

TitaniumAnatasePhotoluminescenceLightPhotoelectron SpectroscopyOrganic ChemistryIonic LiquidsMetal NanoparticlesGeneral ChemistryPhotochemical ProcessesPhotochemistryBiochemistryCatalysischemistry.chemical_compoundUltraviolet visible spectroscopychemistryX-ray photoelectron spectroscopySpectroscopy Fourier Transform InfraredIonic liquidPhotocatalysisHydrothermal synthesisSpectrophotometry UltravioletHOMO/LUMOChemistry - An Asian Journal
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Titania Photocatalysts for Selective Oxidations in Water

2011

Heterogeneous photocatalysis by polycrystalline semiconductor oxides is an unconventional technology that has been mainly applied for the degradation of organic and inorganic pollutants in both the vapor and liquid phase. The application of photocatalysis in synthetic routes has also been researched in recent years, demonstrating its viability as an alternative route in organic chemistry. This work illustrates the main findings in the application of heterogeneous photocatalysis to the oxidation of organic compounds dissolved in water, free of any organic co-solvent. Two main aspects of the oxidative process have been studied: the first one is the partial oxidation of various mono-substitute…

TitaniumTiO2 photocatalysis selective oxidationsChemistryGeneral Chemical EngineeringInorganic chemistryWaterPhotochemical ProcessesHeterogeneous catalysisHydrocarbons AromaticCombinatorial chemistryCatalysisWater PurificationGeneral EnergyAlcoholsEnvironmental ChemistryGeneral Materials ScienceSettore CHIM/07 - Fondamenti Chimici Delle TecnologieOxidation-ReductionEnvironmental Restoration and RemediationWater Pollutants ChemicalChemSusChem
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Photochemistry of oxidized Hg(I) and Hg(II) species suggests missing mercury oxidation in the troposphere.

2020

8 pags., 5 figs., 2 tabs.

atmospheric chemistryAtmospheric chemistry010504 meteorology & atmospheric sciencesTropospheric chemistryMercury photoreductionchemistry.chemical_elementatmospheric modelingAtmospheric model010501 environmental sciencesPhotochemistry01 natural sciencesTroposphereMercury oxidationComputer SimulationGas-phase mercury reactivitygas-phase mercury reactivity0105 earth and related environmental sciencesmercury photoreductionThermal oxidationMultidisciplinaryAtmospherePhotodissociationCorrectionMercuryModels TheoreticalPhotochemical Processestropospheric chemistryMercury (element)Atmospheric modelingDeposition (aerosol physics)chemistry13. Climate actionAtmospheric chemistry[CHIM.OTHE]Chemical Sciences/OtherOxidation-ReductionProceedings of the National Academy of Sciences of the United States of America
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Synthesis and photophysical properties of hyperbranhced polyfluorenes containing 2,4,6-tris(tiophen-2-yl)-1,3,5-triazine as the core

2011

A series of new hyperbranched polymers containing a 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine core unit and polyfluorene chain arms have been synthesized via Suzuki coupling, and characterized by NMR, IR and GPC. All the polymers exhibit good thermal stability with a high decomposition temperature. By changing the 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine/fluorene ratio the UV-vis absorption and emission spectra can be partially tuned. It has been found that the polymers containing a low ratio of 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine units (P1-P3) have an absorption maximum around 385 nm, localized in the polyfluorene chain, and a shoulder around 425 nm ascribable to a charge transfer stat…

chemistry.chemical_classificationFluorenesMolecular StructureAbsorption spectroscopyPolymersTriazinesGeneral Physics and AstronomyThiophenesPolymerFluorenePhotochemical ProcessesPhotochemistryTwo-photon absorptionchemistry.chemical_compoundPolyfluorenechemistryOrganic chemistryPhysical and Theoretical ChemistryAbsorption (chemistry)HOMO/LUMOta116TriazinePhysical Chemistry Chemical Physics
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The Quest for Mononuclear Gold(II) and Its Potential Role in Photocatalysis and Drug Action.

2017

The chemistry of gold strongly focuses on the ubiquitous oxidation states +I and +III. The intermediate oxidation state +II is generally avoided in mononuclear gold species. In recent years, gold(II) has been increasingly suggested as a key intermediate in artificial photosynthesis systems, with gold(III) moieties acting as electron acceptors, as well as in gold-catalyzed photoredox catalysis and radical chemistry. This Minireview provides a concise summary of confirmed and characterized mononuclear open-shell gold(II) complexes. Recent findings on structural motifs and reactivity patterns will be discussed. Exciting developments in the fields of photosynthesis, photocatalysis, and potentia…

chemistry.chemical_classificationMolecular Structure010405 organic chemistryChemistryRadicalChemistry PharmaceuticalPhotoredox catalysisElectronsGeneral ChemistryElectron acceptor010402 general chemistryPhotochemical Processes01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesArtificial photosynthesisElectron transferOxidation statePhotocatalysisOrganic chemistryReactivity (chemistry)Organogold CompoundsAngewandte Chemie (International ed. in English)
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Photosensitization of DNA by β-carbolines: Kinetic analysis and photoproduct characterization

2012

β-Carbolines (βCs) are a group of alkaloids present in many plants and animals. It has been suggested that these alkaloids participate in a variety of significant photosensitized processes. Despite their well-established natural occurrence, the main biological role of these alkaloids and the mechanisms involved are, to date, poorly understood. In the present work, we examined the capability of three important βCs (norharmane, harmane and harmine) and two of its derivatives (N-methyl-norharmane and N-methyl-harmane) to induce DNA damage upon UV-A excitation, correlating the type and extent of the damage with the photophysical characteristics and DNA binding properties of the compounds. The r…

chemistry.chemical_classificationReactive oxygen speciesPhotosensitizing AgentsMolecular StructurebiologySuperoxideSinglet oxygenDNA damageStereochemistryOrganic ChemistryPyrimidine dimerDNAPhotochemical ProcessesBiochemistrySuperoxide dismutaseKineticschemistry.chemical_compoundHarminechemistrybiology.proteinPhysical and Theoretical ChemistryHarmaneReactive Oxygen SpeciesCarbolinesThymidineOrganic & Biomolecular Chemistry
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