Search results for "flash photolysis"

showing 10 items of 34 documents

Photochemical behavior in azobenzene having acidic groups. Preparation of magnetic photoresponsive gels

2011

[EN] The photochemistry of three azobenzenes representing contrasting photochemical behaviors is described in the present work. Thus, Methyl Orange (MO, 4-[[(4-dimethylamino)phenyl]-azo]benzenesulfonic acid sodium salt, hereinafter (1) and 4-hydroxyazobenzene-4'-sulfonic acid (2) undergo in water fast photochemical proton shift, with decays in the microsecond timescale. In contrast to the previous cases, azobenzene-4,4'-dicarboxylic acid (3) undergoes photoisomerization in water. This photochemical behavior allows the preparation of aqueous gels with Aerosil as gelating agent (5% weight) exhibiting high cyclability and photoreversible isomerization of the trans to cis (300 nm irradiation) a…

PhotoisomerizationMagnetismGeneral Chemical EngineeringGeneral Physics and Astronomy02 engineering and technology010402 general chemistryPhotochemistry01 natural scienceschemistry.chemical_compoundQUIMICA ORGANICABenzenesulfonic acidPhotoisomerizationMethyl orangeMagnetite nanoparticlesAqueous solutionAzobenzeneMultifunctional materialsLaser flash photolysisGeneral Chemistry021001 nanoscience & nanotechnologyPhotoresponsive gel0104 chemical sciencesAzobenzenechemistry0210 nano-technologyIsomerizationIron oxide nanoparticlesJournal of Photochemistry and Photobiology A: Chemistry
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Analysis of mebendazole binding to its target biomolecule by laser flash photolysis

2016

[EN] Mebendazole (MBZ) and related anticancer benzimidazoles act binding the beta-subunit of Tubulin (TU) before dimerization with alpha-TU with subsequent blocking microtubule formation. Laser flash photolysis (LFP) is a new tool to investigate drug-albumin interactions and to determine binding parameters such as affinity constant or population of binding sites. The aim of this study was to evaluate the interactions between the nonfluorescent mebendazole (MBZ) and its target biomolecule TU using this technique. Before analyzing the MBZ@TU complex it was needed to determine the photophysical properties of MBZ triplet excited state ((3)MBZ*) in different media. Hence, 3MBZ* showed a transien…

PopulationBiophysicsBinding constantElectron donor010402 general chemistryPhotochemistry01 natural sciencesAnticancer drugschemistry.chemical_compoundQUIMICA ORGANICAMebendazole triplet excited stateTubulinUltrafast laser spectroscopyRadiology Nuclear Medicine and imagingeducationchemistry.chemical_classificationeducation.field_of_studyRadiationPhotolysisRadiological and Ultrasound Technology010405 organic chemistryPhosphorescenceLasersPhotodissociationTemperatureLaser flash photolysisElectron acceptorBinding constant0104 chemical sciencesMebendazolechemistryExcited stateFlash photolysisThermodynamicsSpectrophotometry UltravioletProtein Binding
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Persistent electron-transfer state of a pi-complex of acridinium ion inserted between porphyrin rings of cofacial bisporphyrins

2006

A free-base cofacial bisporphyrin, H(4)DPOx, forms a pi-complex with acridinium ion (AcH(+)) by pi-pi interaction in benzonitrile (PhCN). Formation of the H(4)DPOx-AcH(+) pi-complex was probed by UV-vis and NMR spectroscopy. The binding constant between AcH(+) and H(4)DPOx is determined as 9.7 x 10(4) M(-)(1). Photoinduced electron transfer (ET) from the H(4)DPOx to the AcH(+) moiety occurred efficiently in the pi-complex to form the ET state (H(4)DPOx(*)(+)-AcH(*)). The ET state is successfully detected by laser flash photolysis. The lifetime of the ET state is 18 mus in PhCN at 298 K, and the quantum yield of the ET state is 90%. The temperature dependence of the ET state lifetime has bee…

Quantum yield010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisPhotoinduced electron transferbisporphyrinchemistry.chemical_compoundElectron transferColloid and Surface Chemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistrypie-complexComputingMilieux_MISCELLANEOUS010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyPorphyrin0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryBenzonitrilechemistry[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryFlash photolysisSteady state (chemistry)
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Quaternary structure dependence of kinetic hole burning and conformational substates interconversion in hemoglobin.

2003

Using a sol-gel encapsulation technique, we have prepared samples of CO saturated human adult hemoglobin locked in the R or T quaternary conformation. We report time-resolved spectra of these samples in the Soret region following flash photolysis, in the time interval ranging from 250 ns to 200 ms and in the temperature interval of 100-170 K. A suitable analysis of the measured difference spectra enables us to obtain the spectral contribution of deoxyHb and HbCO molecules as a function of time and/or of the fraction N(t) of deoxyHb molecules. In our experimental time window geminate CO rebinding to hemoglobin in the T quaternary conformation is about 2 orders of magnitude slower than to hem…

Time FactorsChemistryAnalytical chemistryEnergy landscapeflash photolysiKinetic energyLigandsBiochemistrySpectral lineCrystallographyHemoglobinsprotein dynamicTime windowsMoleculeFlash photolysisHumanstime-resolved absorption spectroscopyProtein quaternary structureHemoglobinProtein Structure QuaternaryProtein BindingBiochemistry
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Protein dynamics observed by tunable mid-IR quantum cascade lasers across the time range from 10 ns to 1 s

2017

We have developed a spectrometer based on tunable quantum cascade lasers (QCLs) for recording time-resolved absorption spectra of proteins in the mid-infrared range. We illustrate its performance by recording time-resolved difference spectra of bacteriorhodopsin in the carboxylic range (1800–1700 cm− 1) and on the CO rebinding reaction of myoglobin (1960–1840 cm− 1), at a spectral resolution of 1 cm− 1. The spectrometric setup covers the time range from 4 ns to nearly a second with a response time of 10–15 ns. Absorption changes as low as 1 × 10− 4 are detected in single-shot experiments at t > 1 μs, and of 5 × 10− 6 in kinetics obtained after averaging 100 shots. While previous time-res…

Time FactorsSpectrophotometry InfraredAbsorption spectroscopyAnalytical chemistry010402 general chemistry53001 natural sciencesMolecular physicsSpectral lineAnalytical Chemistrylaw.inventionchannelrhodopsinflash photolysislawSpectral resolutionAbsorption (electromagnetic radiation)InstrumentationSpectroscopyCarbon MonoxidebiologySpectrometerChemistrybacteriorhodopsinLasers010401 analytical chemistry500 Naturwissenschaften und Mathematik::530 Physik::530 PhysikWaterBacteriorhodopsinLasertime-resolved IR spectroscopyAtomic and Molecular Physics and Optics0104 chemical sciencesSolutionsKineticsCascadeBacteriorhodopsinsmyoglobinbiology.proteinQuantum Theory
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Photo Induced Radical Reactions

2012

This article discusses a number of reactions of potential synthetic interest occurring through photochemically generated organic radicals. Emphasis is placed on the nature of the resulting photoproducts, whose formation is discussed on a mechanistic basis. If available, experimental evidence (obtained by laser flash photolysis or related time-resolved techniques) is provided. The material is organized according to the reaction types, for instance, homolytic cleavage, mesolytic cleavage, radical addition, and oxidative or reductive electron transfer. In addition to the classical carboncarbon or carbonhydrogen bond breaking processes, such as the Norrish type I reaction, the hydrogen abstract…

Type I reactionElectron transferChemistryRadicalFlash photolysisBond breakingCleavage (embryo)PhotochemistryHydrogen atom abstractionBond cleavage
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Xanthone-photosensitized detoxification of the veterinary anthelmintic fenbendazole

2013

Fenbendazole (1) is a common veterinary anthelmintic, toxic to water living microorganisms. Fluorescence quantum yields of 1 were found to be 0.11 in acetonitrile, 0.068 in methanol, 0.034 in cyclohexane, and 0.013 in water. The singlet excited state energy was ca. 96 kcal mol(-1) in all solvents. The phosphorescence spectrum of 1 in ethanol at 77 K displayed a maximum at 450 nm, leading to a triplet energy of 75 kcal mol(-1). Experimental excited state energies agree well with the results of OFT calculations at the time-dependent B3LYP/6-311+G(d,p)//B3LYP/6-31G(d) level. Laser flash photolysis (LFP) of 1 at 266 nm led to transients absorbing in the 300-700 nm range, ascribed to radical cat…

Veterinary medicineToxicityChemistryGeneral Chemical EngineeringDaphnia magnaEnvironmental remediationPhotodissociationGeneral Physics and AstronomyMICROBIOLOGIAFenbendazoleGeneral ChemistryPhotochemistrychemistry.chemical_compoundQUIMICA ORGANICARadical ionExcited statePhotodegradationXanthoneBIOQUIMICA Y BIOLOGIA MOLECULARFlash photolysisSinglet statePhotodegradationPhosphorescenceJournal of Photochemistry and Photobiology A: Chemistry
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Structure-dynamics-function relationships in Asian elephant (Elephas maximus) myoglobin. An optical spectroscopy and flash photolysis study on functi…

1993

In this work we report the thermal behavior (10–300 K) of the Soret band lineshape of deoxy and carbonmonoxy derivatives of Asian elephant (Elephas maximus) and horse myoglobins together with their carbon monoxide recombination kinetics after flash photolysis; the results are compared to analogous data relative to sperm whale myoglobin. The Soret band profile is modeled as a Voigt function that accounts for the coupling with high and low frequency vibrational modes, while inhomogeneous broadening is taken into account with suitable distributions of purely electronic transition frequencies. This analysis makes it possible to isolate the various contributions to the overall lineshape that; in…

Voigt profilePhotolysisMyoglobinProtein ConformationPhotodissociationElephantsAnalytical chemistryElectron Spin Resonance SpectroscopyBiophysicsSoft modesMolecular electronic transitionchemistry.chemical_compoundStructure-Activity RelationshipMyoglobinchemistryCarboxyhemoglobinChemical physicsSpectrophotometryMolecular vibrationFlash photolysisAnimalsThermodynamicsHorsesSpectroscopyResearch ArticleBiophysical Journal
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Iodine and mercury resonance lamps for kinetics experiments and their spectra in the far ultraviolet

2000

Electrodeless iodine and mercury iodide radio-frequency discharge lamps have been made to provide intense sources of resonance radiation of iodine and mercury in the 183-253 nm region. Production technology and emission spectra in the ultraviolet and vacuum ultraviolet regions are described. Both lamps (iodine and mercury iodide) are designed and used for monitoring the iodine 2P1/2 (206.163 nm) and 2P3/2 (183.038 nm) level population kinetics after flash photolysis of I2 or other precursor molecules in laboratory experiments. The technique is suitable for the investigation of the gas phase reaction kinetics following the photolysis of I2 in the presence of O3.

chemistry.chemical_classificationGas-discharge lampAcoustics and UltrasonicsKineticsPhotodissociationIodideAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsIodinemedicine.disease_causeSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionMercury (element)chemistrylawmedicineFlash photolysisUltravioletJournal of Physics D: Applied Physics
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The triplet excited state of the biocative compound thiabendazole. Characterization and suitability as reporter for cyclodextrin complexation

2012

Fluorescence spectroscopy, laser flash photolysis (LPF), and density functional theory calculations have been performed to characterize the photobehavior of thiabendazole (1). Direct LFP of 1 results in the generation of a transient absorbing at λmax = 570 nm identified as the triplet excited state (31∗). The intersystem crossing quantum yield is 0.91, and the triplet energy is 288 kJ mol−1. The singlet–triplet energy gap is 84 kJ mol−1. The behavior of thiabendazole within CDs results in a marked enhancement of the triplet lifetime, this change is attributed to the mobility restrictions of included 1 imposed by the cyclodextrin cavities.

chemistry.chemical_classificationOptimizationCyclodextrinBeta-CyclodextrinGeneral Physics and AstronomyQuantum yieldHuman-SerumDensityProteinsPhotochemistryPolarizable continuum modelBenzimidazoleFluorescence spectroscopyIntersystem crossingQUIMICA ORGANICAchemistryExcited stateSolventTransitionFlash photolysisPolarizable continuum modelDensity functional theoryPhysical and Theoretical ChemistryApproximation
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