Search results for "photodissociation"

showing 10 items of 90 documents

Photoinduced chemiluminescence of pharmaceuticals

2005

Abstract A screening test for the forward development of chemiluminescence systems able to determine pharmaceutical compounds is reported. The test is based on the on-line photodegradation of the drugs by using a photoreactor consisting of 697 cm × 0.5 mm PTFE tubing helically coiled around an 8 W low-pressure mercury lamp. Photodegraded pharmaceuticals are detected by direct chemiluminescence of the resulting photofragments and their subsequent reaction with potassium permanganate in sulphuric acid medium as oxidant. The screening comprised 97 compounds with different molecular structures and relevant members of the most important families of pharmaceuticals are tested (amino acids, carbox…

LuminescenceLightScreening testPhotochemistryClinical BiochemistryPharmaceutical Sciencebeta-LactamsAnalytical Chemistrylaw.inventionStructure-Activity Relationshipchemistry.chemical_compoundAlkaloidsOxidants PhotochemicalPotassium PermanganatePhenothiazineslawDrug DiscoverymedicineOrganic chemistryEphedrinePhotodegradationSpectroscopyChemiluminescencechemistry.chemical_classificationBicyclic moleculePhotodissociationHydrogen-Ion ConcentrationAmino acidPotassium permanganatePharmaceutical Preparationschemistrymedicine.drugJournal of Pharmaceutical and Biomedical Analysis
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Structural factors controlling ligand binding to myoglobin: a kinetic hole-burning study.

1998

Using temperature-derivative spectroscopy in the temperature range below 100 K, we have studied the dependence of the Soret band on the recombination barrier in sperm whale carbonmonoxy myoglobin (MbCO) after photodissociation at 12 K. The spectra were separated into contributions from the photodissociated species, Mb*CO, and CO-bound myoglobin. The line shapes of the Soret bands of both photolyzed and liganded myoglobin were analyzed with a model that takes into account the homogeneous bandwidth, coupling of the electronic transition to vibrational modes, and static conformational heterogeneity. The analysis yields correlations between the activation enthalpy for rebinding and the model p…

MaleMultidisciplinaryBinding SitesProtein ConformationSpectrum AnalysisPhotodissociationEnthalpyWhalesBiological SciencesLigandsSpermatozoaMolecular electronic transitionSpectral lineCrystallographychemistry.chemical_compoundMyoglobinchemistryChemical physicsMolecular vibrationAnimalsSpectroscopyMetmyoglobinHemeProtein BindingProceedings of the National Academy of Sciences of the United States of America
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Regiochemical memory in the adiabatic photolysis of thymine-derived oxetanes. A combined ultrafast spectroscopic and CASSCF/CASPT2 computational stud…

2020

[EN] The photoinduced cycloreversion of oxetanes has been thoroughly investigated in connection with the photorepair of the well-known DNA (6-4) photoproducts. In the present work, the direct photolysis of the two regioisomers arising from the irradiation of benzophenone (BP) and 1,3-dimethylthymine (DMT), namely the head-to-head (HH-1) and head-to-tail (HT-1) oxetane adducts, has been investigated by combining ultrafast spectroscopy and theoretical multiconfigurational quantum chemistry analysis. Both the experimental and computational results agree with the involvement of an excited triplet exciplex(3)[BPMIDLINE HORIZONTAL ELLIPSISDMT]* for the photoinduced oxetane cleavage to generate(3)…

Materials science010405 organic chemistryPhotodissociationGeneral Physics and Astronomy010402 general chemistryOxetanePhotochemistry01 natural sciencesQuantum chemistry0104 chemical scienceschemistry.chemical_compoundQUIMICA ORGANICAIntersystem crossingchemistryExcited stateUltrafast laser spectroscopyBenzophenonePhysical and Theoretical ChemistryGround statePhysical chemistry chemical physics : PCCP
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Ab initio quantum-chemical computations of the absorption cross sections of HgX2 and HgXY (X, y = Cl, Br, and I): Molecules of interest in the Earth'…

2018

13 pags., 4 figs., 2 tabs.

Materials sciencePhotodissociationAb initioGeneral Physics and AstronomyHalide02 engineering and technologyElectronic structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physicsSpectral line0104 chemical sciencesMoleculePhysical and Theoretical Chemistry0210 nano-technologyBasis setOrder of magnitudePhysical Chemistry Chemical Physics 21: 455-467 (2019)
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Gas-Phase Photolysis of Hg(I) Radical Species: A New Atmospheric Mercury Reduction Process

2019

The efficient gas-phase photoreduction of Hg(II) has recently been shown to change mercury cycling significantly in the atmosphere and its deposition to the Earth's surface. However, the photolysis of key Hg(I) species within that cycle is currently not considered. Here we present ultraviolet-visible absorption spectra and cross-sections of HgCl, HgBr, HgI, and HgOH radicals, computed by high-level quantum-chemical methods, and show for the first time that gas-phase Hg(I) photoreduction can occur at time scales that eventually would influence the mercury chemistry in the atmosphere. These results provide new fundamental understanding of the photobehavior of Hg(I) radicals and show that the …

Mercury cyclingAbsorption spectroscopyChemistryRadicalPhotodissociationAtmospheric mercurychemistry.chemical_elementGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciences7. Clean energyBiochemistryCatalysis0104 chemical sciencesGas phaseMercury (element)Colloid and Surface Chemistry13. Climate actionGlobal distribution
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Autonomous artificial nanomotor powered by sunlight

2006

Light excitation powers the reversible shuttling movement of the ring component of a rotaxane between two stations located at a 1.3-nm distance on its dumbbell-shaped component. The photoinduced shuttling movement, which occurs in solution, is based on a “four-stroke” synchronized sequence of electronic and nuclear processes. At room temperature the deactivation time of the high-energy charge-transfer state obtained by light excitation is ≈10 μs, and the time period required for the ring-displacement process is on the order of 100 μs. The rotaxane behaves as an autonomous linear motor and operates with a quantum efficiency up to ≈12%. The investigated system is a unique example of an artif…

Models MolecularLuminescenceMagnetic Resonance SpectroscopyTime FactorsRotaxaneLightRotaxanesUltraviolet RaysPhotochemistryMovementMolecular ConformationElectronsPhotochemistryAbsorptionQUIMICA ORGANICAPhenothiazinesRotaxaneElectrochemistryNanotechnologyNanomotorAbsorption (electromagnetic radiation)Molecular machinePhotolysisMultidisciplinaryChemistrybusiness.industryMolecular Motor ProteinsPhotodissociationTemperatureLinear motorKineticsNanoscienceFluid solutionSpectrophotometryPhysical SciencesSunlightOptoelectronicsQuantum efficiencyElectronicsLuminescencebusinessSupramolecular chemistry
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High Pressure Enhances Hexacoordination in Neuroglobin and Other Globins

2005

The techniques of high applied pressure and flash photolysis have been combined to study ligand rebinding to neuroglobin (Ngb) and tomato Hb, globins that may display a His-Fe-His hexacoordination in the absence of external ligands. High pressure induces a moderate decrease in the His association rate and a large decrease in His dissociation rate, thus leading to an enhancement of the overall His affinity. The overall structural difference between penta- and hexacoordinated globins may be rather small and can be overcome by external modifications such as high pressure. Over the pressure range 0.1-700 MPa (7 kbar), the globins may show a loss of over a factor of 100 in the amplitude of the b…

Models MolecularSteric effectsProtein ConformationStereochemistryIronNeuroglobinchemistry.chemical_elementNerve Tissue ProteinsHemeLigandsBiochemistryOxygenHemoglobinschemistry.chemical_compoundSolanum lycopersicumPressureAnimalsHumansHistidineHorsesGlobinMolecular BiologyHemeBinding SitesPhotolysisMyoglobinChemistryPhotodissociationHeartCell BiologyLigand (biochemistry)GlobinsOxygenKineticsNeuroglobinBiophysicsFlash photolysisProtein BindingJournal of Biological Chemistry
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Different relaxations in myoglobin after photolysis

2004

To clarify the interplay of kinetic hole-burning (KHB), structural relaxation, and ligand migration in myoglobin (Mb), we measured time-resolved absorption spectra in the Soret region after photolysis of carbon monoxide Mb (MbCO) in the temperature interval 120-260 K and in the time window 350 ns to 200 ms. The spectral contributions of both photolyzed (Mb * ) and liganded Mb (MbCO) have been analyzed by taking into account homogeneous bandwidth, coupling to vibrational modes, and static conformational heterogeneity. We succeeded in separating the “time-dependent” spectral changes, and this work provides possibilities to identify the events in the process of ligand rebinding. KHB is domina…

Myoglobin Molecular Dynamics Simulation active siteAbsorption spectroscopyKineticsAnalytical chemistryThermodynamicsIn Vitro TechniquesKinetic energyLigandschemistry.chemical_compoundAnimalsMultidisciplinaryBinding SitesPhotolysisLigandMyoglobinPhotodissociationTemperatureWhalesBiological SciencesKineticsMyoglobinchemistrySpectrophotometryMolecular vibrationThermodynamicsCarbon monoxide
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Molecular tunneling and pumping effects in low temperature MBCO recombination

1992

Recombination of carbonmonoxide after photodissociation has been studied by Mossbauer spectroscopy at 4.2K and in the low temperature region, where tunneling effects play an important role in rebinding. We interpret the kinetic results in terms of a radiationless nonadiabatic multiphonon transition, which leads to a uniform description for all temperatures. Prolonged illumination at low temperature results in pumping into long-living states.

Nuclear and High Energy PhysicsChemical physicsChemistryMössbauer spectroscopyPhotodissociationPhysical and Theoretical ChemistryAtomic physicsCondensed Matter PhysicsKinetic energyAtomic and Molecular Physics and OpticsQuantum tunnellingRecombinationHyperfine Interactions
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Recombination studies of photodissociated MbCO by Mössbauer spectroscopy at low temperatures

1990

Rebinding of carbonmonoxide to myoglobin after photodissociation has been studied by Mossbauer spectroscopy at 57.6 K and below for up to 9 days. The time dependence is reproduced by a set of exponentials representing a distribution of activation enthalpies. A shift to smaller values of these activation enthalpies and of the preexponential factor compared to optical studies at higher temperatures has been observed as well as pumping into long-living states.

Nuclear and High Energy PhysicsChemistryEnthalpyPhotodissociationAnalytical chemistryCondensed Matter PhysicsAtomic and Molecular Physics and Opticschemistry.chemical_compoundMyoglobinComputational chemistryMössbauer spectroscopyPhysical and Theoretical ChemistryThin filmSpectroscopyRecombinationHyperfine Interactions
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