Search results for "PHOTOCHEMISTRY"

showing 10 items of 2034 documents

Halogen-containing BODIPY derivatives for photodynamic therapy

2019

Abstract Two iodinated (1 and 2) and two brominated (3 and 4) BODIPY-based photosensitizers are prepared and characterized using slightly modified synthetic procedures previously described. 1–4 present intense absorption bands in the 510–540 nm interval and very weak emissions due to the presence of halogen atoms in their structure. Irradiation of aqueous solutions of 1–4 with visible light (wavelength > 475 nm) induce the generation of singlet oxygen with quantum yields of ca. 0.62–0.66 for the photosensitizers containing iodine atoms (1 and 2) and of ca. 0.16–0.21 for the brominated counterparts (3 and 4). In vitro studies carried out with HeLa, SCC-13 and HaCaT cell lines and the four ph…

Aqueous solutionbiologySinglet oxygenProcess Chemistry and TechnologyGeneral Chemical Engineeringmedicine.medical_treatmentPhotodynamic therapy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologybiology.organism_classificationPhotochemistry01 natural sciences0104 chemical sciencesHeLachemistry.chemical_compoundHaCaTchemistryHalogenmedicineBODIPY0210 nano-technologyVisible spectrumDyes and Pigments
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Electrochemistry, spectroelectrochemistry, chloride binding, and O2 catalytic reactions of free-base porphyrin-cobalt corrole dyads.

2005

Three face-to-face linked porphyrin-corrole dyads were investigated as to their electrochemistry, spectroelectrochemistry, and chloride-binding properties in dichloromethane or benzonitrile. The same three compounds were also investigated as to their ability to catalyze the electroreduction of dioxygen in aqueous 1 M HClO4 or HCl when adsorbed on a graphite electrode. The characterized compounds are represented as (PCY)H2Co, where P = a porphyrin dianion; C = a corrole trianion; and Y = a biphenylenyl, 9,9-dimethylxanthenyl, or anthracenyl spacer, which links the two macrocycles in a face-to-face arrangement. An axial binding of one or two Cl- ligands to the cobalt center of the corrole is …

Aqueous solutionchemistry.chemical_elementFree baseElectrochemistryPhotochemistryPorphyrinCatalysisInorganic Chemistrychemistry.chemical_compoundBenzonitrilechemistryPolymer chemistryPhysical and Theoretical ChemistryCorroleCobaltInorganic chemistry
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A fluorescent chemosensor based on a ruthenium(II)-terpyridine core containing peripheral amino groups that selectively sense ATP in an aqueous envir…

2000

The selective sensing of the ATP anion in an aqueous environment over phosphate, sulfate, and chloride using a fluorescence chemosensor based on Ru(tpy)22+ cores attached to polyammonium groups is reported.

Aqueous solutionchemistry.chemical_elementPhosphatePhotochemistryFluorescenceChlorideRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryparasitic diseasesSense (molecular biology)Polymer chemistryMaterials ChemistrymedicinePhysical and Theoretical ChemistrySulfateTerpyridinemedicine.drugInorganic Chemistry Communications
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V2O5 nanowires with an intrinsic iodination activity leading to the formation of self-assembled melanin-like biopolymers

2011

V2O5 nanowires act as biomimetic catalysts resembling vanadium haloperoxidases (V-HPO). The nanowires display iodinating activity as confirmed by a colorimetric assay using thymol blue (TB), UV/Vis spectrophotometry and mass spectrometry (FD-MS). In the presence of dopamine these nanowires catalyze the fast and efficient synthesis of melanin-like biopolymers under mild conditions (aqueous solution, neutral pH and room temperature). The resulting melanin-like biopolymer obtained by the V2O5 nanowire catalysts was characterized by scanning electron microscopy (SEM), X-ray diffraction, UV-Vis, FT-IR and electric conductivity resembling the natural biopolymer both in its chemical and morphologi…

Aqueous solutionmedicine.diagnostic_testChemistryScanning electron microscopeNanowireVanadiumchemistry.chemical_elementGeneral ChemistryThymol blueengineering.materialPhotochemistryCatalysischemistry.chemical_compoundSpectrophotometryMaterials ChemistrymedicineengineeringOrganic chemistryBiopolymerJournal of Materials Chemistry
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Light-induced opening and closing of the intramolecular hydrogen bond in glyoxylic acid.

2013

The isomerization process of glyoxylic acid (GA) conformers and their complexes with a water molecule were studied in a low temperature argon matrix. The research target was to understand how starting conformation and complexation affects the near-IR (NIR) induced conformer interconversion. The most stable GA conformer (Tc) is characterized by an intramolecular hydrogen bond, and it is found to undergo light-induced conformer interconversion slower than the open (Tt) conformer. Upon complexation with water, the isomerization processes slow down in the case of the Tc conformer, whereas for the Tt-based complex the influence of water is negligible on the isomerization process.

ArgonChemistryHydrogen bondchemistry.chemical_elementPhotochemistrychemistry.chemical_compoundIntramolecular forceLight inducedMoleculePhysical and Theoretical ChemistryConformational isomerismIsomerizationta116Glyoxylic acidThe journal of physical chemistry. A
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Raman spectroscopy and high-overtone driven isomerization of glyoxylic acid in solid argon

2013

High-overtone induced chemistry of glyoxylic acid isolated in a low-temperature argon matrix was investigated using Raman spectroscopy. The Raman spectra of two most stable conformers of glyoxylic acid are presented. Upon excitation in high overtone vibrational bands by 532 nm irradiation of the lowest energy conformer most abundant in neat deposited sample, the isomerization of glyoxylic acid was observed. The process most plausible proceeds via absorption into the fifth vibrational overtone state of the OH group or its combination with the torsional vibrational transition. The assignment of the fundamental vibrational spectra was assisted by quantum chemical harmonic and anharmonic vibrat…

ArgonOvertoneAnharmonicitychemistry.chemical_elementPhotochemistrychemistry.chemical_compoundsymbols.namesakechemistryPhysics::Atomic and Molecular ClusterssymbolsRadiology Nuclear Medicine and imagingPhysics::Chemical PhysicsAbsorption (chemistry)Raman spectroscopyConformational isomerismIsomerizationGlyoxylic acidBiomedical Spectroscopy and Imaging
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Superficial defects induced by argon and oxygen bombardments on (110) TiO2 surfaces

1998

Abstract Compositional and chemical changes of titanium dioxide monocrystalline surfaces induced by bombardment with 4 keV argon and oxygen ions have been studied by AES, XPS and AFM. Argon ion bombardment induced strong changes in the composition and chemical state of the surface: loss of oxygen due to preferential sputtering occurred, and, related to this, Ti4+ species were reduced to Ti3+ and Ti2+. During oxygen bombardment, competition between preferential sputtering of oxygen ions of the oxide surface and oxygen implantation was observed. This phenomenon was found to be strongly dependent upon the incidence angle of the oxygen ions. Moreover, an oxygen bombardment with normal incidence…

ArgonOxidechemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsPhotochemistryOxygenSurfaces Coatings and FilmsMonocrystalline siliconCondensed Matter::Materials ScienceChemical statechemistry.chemical_compoundchemistryX-ray photoelectron spectroscopyPhysics::Plasma PhysicsSputteringTitanium dioxideMaterials Chemistrysense organsPhysics::Chemical PhysicsNuclear chemistrySurface Science
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Efficient ultraviolet-light energy dissipation by an aromatic ketone.

2010

Experimental evidence on the efficiency of 2,2'4,4'-tetramethoxybenzil for UV-light energy dissipation is provided. This non-phenolic aromatic ketone has a low energy triplet which quickly decays to the ketone ground state, thus avoiding the generation of undesirable reactive species. El Moncef, Abdelkarim, elmonab@alumni.uv.es ; Cuquerella Alabort, Maria Consuelo, Chelo.Cuquerella@uv.es ; Zaballos Garcia, Elena, Elena.Zaballos@uv.es ; Ramirez de Arellano Sanchez, Maria del Carmen, Carmen.Ramirezdearellano@uv.es ; Stiriba, Salah Eddine, Salah.Stiriba@uv.es ; Perez Prieto, Julia, Julia.Perez@uv.es

Aromatic ketoneKetoneUltraviolet RaysUNESCO::QUÍMICAUV-lightPhotochemistry:QUÍMICA [UNESCO]CatalysisLow energyMaterials ChemistryUltraviolet lightTetramethoxybenzil ; UV-light ; Reactive ; Aromatic KetoneAromatic Ketonechemistry.chemical_classificationMolecular StructureUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistryDissipationKetonesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryReactiveCeramics and Composites:QUÍMICA::Química analítica [UNESCO]TetramethoxybenzilGround stateChemical communications (Cambridge, England)
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Methyl vinyl ketone+OH and methacrolein+OH oxidation reactions: a master equation analysis of the pressure- and temperature-dependent rate constants.

2006

High-level electronic structure calculations and master equation analyses were carried out to obtain the pressure- and temperature-dependent rate constants of the methyl vinyl ketone+OH and methacrolein+OH reactions. The balance between the OH addition reactions at the high-pressure limit, the OH addition reactions in the fall-off region, and the pressure-independent hydrogen abstractions involved in these multiwell and multichannel systems, has been shown to be crucial to understand the pressure and temperature dependence of each global reaction. In particular, the fall-off region of the OH addition reactions contributes to the inverse temperature dependence of the rate constants in the Ar…

Arrhenius equationAddition reactionHydrogenChemistryOrganic Chemistrychemistry.chemical_elementMethacroleinGeneral ChemistryPhotochemistryHydrogen atom abstractionRedoxCatalysischemistry.chemical_compoundsymbols.namesakeReaction rate constantMethyl vinyl ketonesymbolsChemistry (Weinheim an der Bergstrasse, Germany)
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Intersystem crossing in Fe(II) coordination compounds

1994

Fe(II) spin-crossover systems can be quantitatively converted from the low-spin (LS) to the high-spin (HS) state well below the thermal transition temperature by irradiating either into the metal-ligand charge transfer or d-d absorption bands, and even in low-spin systems a transient population of the HS state can be achieved. This fact can be made use of to determine HS → LS relaxation rate constants for a wide variety of Fe(II) spin-crossover and low-spin systems. The HS → LS relaxation shows strong deviations from an Arrhenius behaviour, with nearly temperature-independent tunnelling below ∼70 K and a thermally activated process above ∼100 K. The range of more than 12 orders of magnitude…

Arrhenius equationNuclear and High Energy Physicseducation.field_of_studyChemistryPopulationCondensed Matter PhysicsInternal conversion (chemistry)PhotochemistryMolecular physicsAtomic and Molecular Physics and OpticsVibronic couplingsymbols.namesakeIntersystem crossingReaction rate constantsymbolsRelaxation (physics)Physical and Theoretical ChemistryeducationQuantum tunnellingHyperfine Interactions
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