Search results for "Photochemistry"

showing 10 items of 2034 documents

Electrochemistry and spectroelectrochemistry of bismanganese biscorroles dyads

2011

Three manganese biscorrole dyads were synthesized, physicochemically characterized and investigated as to their electrochemistry and spectroelectrochemistry in nonaqueous media. Each dyad contained the same two corroles linked in a face-to-face arrangement via one of the three different linking groups, 9,9-dimethylxanthene, anthracene or diphenylether, the exact nature of which determined the distance and possible interaction between the two metallomacrocycles. The initial compounds contained Mn ( III ) in their air stable form and were shown to exhibit two major redox processes, one being a Mn (III)/ Mn (IV) conversion and the other being either Mn ( III )/ Mn ( II ) or reduction at the c…

Anthracenechemistry.chemical_elementGeneral ChemistryManganeseConjugated systemElectrochemistryPhotochemistryRedoxchemistry.chemical_compoundElectron transferchemistryPyridinePolymer chemistryCorroleJournal of Porphyrins and Phthalocyanines
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Electronic Interactions in a New π-Extended Tetrathiafulvalene Dimer

2006

The first pi-extended tetrathiafulvalene (exTTF) dimer in which the two exTTF units are covalently connected by 1,3-dithiole rings has been obtained in a multistep synthetic procedure involving the Ullmann cross-coupling reaction by using copper(I) thiophene-2-carboxylate (CuTC). The electronic spectrum reveals a significant electronic interaction between the exTTF units. The electrochemical study carried out by cyclic voltammetry in solution and in thin-layer conditions, and the electrochemical simulation and spectroelectrochemical (SEC) measurements confirm the electronic communication and show that the oxidation of dimer 14 occurs as two consecutive 2 e(-) processes D(0)-D(0)-->D(2+)-D(0…

AnthracenesAnthraceneDimerOrganic Chemistrychemistry.chemical_elementStereoisomerism[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryPhotochemistryElectrochemistryCopperCatalysisDelocalized electronchemistry.chemical_compoundCrystallographyModels ChemicalchemistryHeterocyclic CompoundsCovalent bondElectrochemistryElectronicsCyclic voltammetryDimerizationOxidation-ReductionTetrathiafulvaleneChemistry - A European Journal
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Intramolecular electronic excitation energy transfer in donor∕acceptor dyads studied by time and frequency resolved single molecule spectroscopy

2008

Electronic excitation energy transfer has been studied by single molecule spectroscopy in donor/acceptor dyads composed of a perylenediimide donor and a terrylenediimide acceptor linked by oligo(phenylene) bridges of two different lengths. For the shorter bridge (three phenylene units) energy is transferred almost quantitatively from the donor to the acceptor, while for the longer bridge (seven phenylene units) energy transfer is less efficient as indicated by the occurrence of donor and acceptor emission. To determine energy transfer rates and efficiencies at the single molecule level, several methods have been employed. These comprise time-correlated single photon counting techniques at r…

AnthracenesTime FactorsLightMolecular StructurePhotochemistryChemistryTemperatureGeneral Physics and AstronomyElectronsP680ElectronImidesAcceptorMolecular electronic transitionSpectrometry FluorescenceEnergy TransferPhenyleneIntramolecular forceExcited statePolycyclic Aromatic HydrocarbonsPhysical and Theoretical ChemistryAtomic physicsPeryleneExcitationThe Journal of Chemical Physics
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Synthesis and evaluation of diverse thio avarol derivatives as potential UVB photoprotective candidates.

2007

Semisynthesis of 13 new thio avarol derivatives (4-16) and in vitro evaluation on the photodamage response induced by UVB irradiation are described. Their ability to inhibit NF-kappaB activation and TNF-alpha generation in HaCaT cells as well as their antioxidant capacity in human neutrophils has also been studied. Among them we have identified two monophenyl thio avarol derivatives (4-5) lacking cytotoxicity which can be considered promising UVB photoprotective agents through the potent inhibition of NF-kappaB activation with a mild antioxidant pharmacological profile.

AntioxidantMagnetic Resonance SpectroscopyNeutrophilsPhotochemistryUltraviolet Raysmedicine.medical_treatmentChemistry PharmaceuticalClinical BiochemistryMolecular ConformationPharmaceutical ScienceThio-BiochemistryChemical synthesisAntioxidantsCell Line TumorDrug DiscoverymedicineHumansCytotoxicityMolecular Biologyintegumentary systemChemistryTumor Necrosis Factor-alphaOrganic ChemistryNF-kappa BSemisynthesisIn vitroHaCaTmedicine.anatomical_structureBiochemistryModels ChemicalDrug DesignMolecular MedicineKeratinocyteReactive Oxygen SpeciesSesquiterpenesBioorganicmedicinal chemistry letters
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Antioxidant reactions of all-trans retinol in phospholipid bilayers: effect of oxygen partial pressure, radical fluxes, and retinol concentration.

1997

Lipoperoxyl radical-scavenging activity of retinol in unilamellar soybean phosphatidylcholine liposomes was studied under a variety of conditions to appreciate to what extend retinol may be considered an effective antioxidant. Peroxidation, initiated by 2 mM 2,2'-azobis(amidino-propane)hydrochloride (AAPH), was carried out at 160 torr O2 or at 15 torr O2, in the absence or in the presence of 10 to 40 mM retinol. As evaluated by the length of the inhibition periods, t(inh), and by the ratio between the inhibition and propagation rate, R(inh)/R(p), the antioxidant activity of retinol was higher at 15 torr O2 than at 160 torr O2. The consumption rate of retinol was markedly faster at 160 torr …

Antioxidantgenetic structuresFree Radicalsmedicine.medical_treatmentLipid BilayersBiophysicsPhospholipidchemistry.chemical_elementPhotochemistryBiochemistryOxygenAntioxidantschemistry.chemical_compoundLipid oxidationPhosphatidylcholinemedicineButylated hydroxytolueneAll trans retinolVitamin AMolecular BiologyPhospholipidsChromatographyRetinolFree Radical ScavengersCarbonOxygenchemistryLiposomesRetinaldehydeDiterpenesArchives of biochemistry and biophysics
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Selective chromo-fluorogenic detection of trivalent cations in aqueous environments using a dehydration reaction

2016

[EN] Trivalent cations (Al3+, Fe3+, Cr3+, As3+, In3+ and Ga3+) induced a dehydration reaction of a chemodosimeter in water that is coupled with colour and emission changes.

Aqueous solution010405 organic chemistryChemistryQUIMICA INORGANICAInorganic chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesQUIMICA ORGANICADehydration reactionMaterials ChemistryQualitative inorganic analysisNew Journal of Chemistry
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Converting p-terphenyl into a novel organo-catalyst for LED-driven energy and electron transfer photoreactions in water.

2021

p-Terphenyl is a potent photoredox catalyst under UV-irradiation. Aiming for more sustainable reaction conditions, we added two sulfonate groups to this key structure to achieve water solubility and incorporated an SO2-bridge thereby shifting the absorption spectrum towards the visible. The resulting photocatalyst shows unexpected triplet reactivity in several test reactions.

Aqueous solutionAbsorption spectroscopyMetals and AlloysGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundElectron transferSulfonatechemistryTerphenylMaterials ChemistryCeramics and CompositesPhotocatalysisReactivity (chemistry)Chemical communications (Cambridge, England)
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Photocatalytic oxidation of phenol on TiO2 powders. A Fourier transform infrared study

1994

Abstract In the present paper a detailed investigation of a well known photoreaction, i.e. phenol photodegradation in the presence of TiO2, has been carried out. The Fourier transform infrared (FT-IR) technique has been used to characterize the catalyst surface and to follow the photoprocess by “in situ” measurements in a gas—solid regime, simulating the aqueous liquid—solid regime in which this photodegradation reaction has been usually carried out. The influence on the photoprocess of the surface hydroxylation of the catalyst has been investigated and the presence of some reaction intermediates has been revealed by FT-IR. The experimental results have demonstrated that the chosen gas—soli…

Aqueous solutionAdsorptionChemistryProcess Chemistry and TechnologyPhotocatalysisInfrared spectroscopyReaction intermediateFourier transform infrared spectroscopyPhotodegradationPhotochemistryCatalysisGeneral Environmental ScienceCatalysisApplied Catalysis B: Environmental
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Interaction between nitroxyl radicals and CdTe quantum dots: Determination of fluorescence-quenching mechanisms in aqueous solution

2019

Abstract The present work characterizes the optical properties of CdTe quantum dots (CdTe QDs) after interaction with nitroxyl radicals based on steady-state and time-resolved fluorescence spectroscopy studies. QDs of different sizes were exposed to 2 different nitroxyl radicals, i.e., TEMPO and 4-amino-TEMPO radicals. A clear dependence of dynamic and static Stern-Volmer constants values, KD and KS, respectively, was observed as a function of the size of QDs used, with a change from a mostly static mechanism (for smaller QD sizes) to a dynamic mechanism predominating as the nanoparticles increase in size. All observed effects are dependent on both the concentration of the radical and the s…

Aqueous solutionAqueous mediumChemistryGeneral Chemical EngineeringRadicalGeneral Physics and AstronomyNanoparticle02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesCadmium telluride photovoltaicsFluorescence spectroscopy0104 chemical sciencesNitroxyl radicalsQuantum dot0210 nano-technologyJournal of Photochemistry and Photobiology A: Chemistry
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Unusual redox play of Mo(V/IV) during oxidative aryl–aryl coupling

2012

The oxidative treatment of a suitable 1,3-diarylpropene precursor by MoCl5 causes a series of redox steps yielding a dimer of dibenzo[a,c]cycloheptene. After the oxidative aryl–aryl bond formation, a C,H activation occurs providing a tropylium intermediate. Upon aqueous workup the metal waste acts as reductive media generating the dimer in an almost quantitative manner. The oxidative generation of the tropylium species as well as the subsequent redox play by the metal waste is unique and unprecedented. The dimeric compound can be oxidatively cleaved and subsequently decarboxylated providing the key intermediate of a previous synthesis of metasequirin-B derivatives.

Aqueous solutionArylDimerOrganic ChemistryOxidative phosphorylationPhotochemistryBiochemistryRedoxMedicinal chemistryMetalchemistry.chemical_compoundchemistryvisual_artDrug Discoveryvisual_art.visual_art_mediumCyclohepteneOxidative coupling of methaneTetrahedron Letters
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