Search results for "hydroxyl radical"

showing 10 items of 65 documents

Effect of protonation and deprotonation on the gas phase reactivity of fluorinated 1,2,4-triazines

2008

Positive and negative electrospray mass spectrometry (MS), in-time and in-space MS n experiments, high-resolution and accurate mass measurements obtained with an Orbitrap, together with density functional theory calculations have been used to study the gas-phase ion chemistry of a series of fluorinated 1,2,4-triazines. As a result of low-energy collision-induced dissociations, occurring in an ion trap and in a triple quadrupole, their protonated and deprotonated molecules show interesting features depending on the nature and structure of the precursor ions. The occurrence of elimination/hydration reactions produced by positive ions in the ion trap is noteworthy. Decompositions of deprotonat…

Models MolecularSpectrometry Mass Electrospray IonizationIONIZATION MASS-SPECTROMETRYFluorine CompoundsAnalytical chemistryProtonationTandem mass spectrometryPhotochemistryOrbitrapIonlaw.inventionchemistry.chemical_compoundDeprotonationStructural BiologylawCHEMISTRYMoleculeComputer SimulationPhysics::Chemical PhysicsNEGATIVE ELECTROSPRAY-IONIZATIONCOLLISION-INDUCED DISSOCIATIONSpectroscopyTRIAZINESHYDRAZINEchemistryModels ChemicalHydroxyl radicalIon trapProtonsFRAGMENTATIONHETEROCYCLES
researchProduct

Theoretical Study of the Hydroxyl Radical Addition to Uracil and Photochemistry of the Formed U6OH• Adduct

2014

Hydroxyl radical ((•)OH) is produced in biological systems by external or endogenous agents. It can damage DNA/RNA by attacking pyrimidine nucleobases through the addition to the C5═C6 double bond. The adduct resulting from the attachment at the C5 position prevails in the experimental measurements, although the reasons for this preference remain unclear. The first aim of this work is therefore to shed light on the comprehension of this important process. Thus, the thermal (•)OH addition to the C5═C6 double bond of uracil has been studied theoretically by using DFT, MP2, and the multiconfigurational CASPT2//CASSCF methodologies. The in-vacuo results obtained with the latter protocol plus th…

Models Molecularchemistry.chemical_classificationPyrimidineDouble bondHydroxyl RadicalPhotochemistryUracilPhotochemistrySurfaces Coatings and FilmsAdductNucleobaseDNA Adductschemistry.chemical_compoundchemistryMaterials ChemistryQuantum TheoryHydroxyl radicalPhysical and Theoretical ChemistrySolvent effectsUracilVisible spectrumThe Journal of Physical Chemistry B
researchProduct

Communication: Electronic UV-Vis transient spectra of the ·OH reaction products of uracil, thymine, cytosine, and 5,6-dihydrouracil by using the comp…

2013

Addition of ∙OH radicals to pyrimidine nucleobases is a common reaction in DNA/RNA damage by reactive oxygen species. Among several experimental techniques, transient absorption spectroscopy has been during the last decades used to characterize such compounds. Discrepancies have however appeared in the assignment of the adduct or adducts responsible for the reported transient absorption UV-Vis spectra. In order to get an accurate assignment of the transient spectra and a unified description of the absorption properties of the ∙OH reaction products of pyrimidines, a systematic complete active space self-consistent field second-order perturbation (CASPT2//CASSCF) theory study has been carried…

Molecular StructurePyrimidineHydroxyl RadicalGeneral Physics and AstronomyDihydrouracilElectronsUracilHydrogen atom abstractionPhotochemistryThymineAdductNucleobaseCytosinechemistry.chemical_compoundchemistryComputational chemistryQuantum TheorySpectrophotometry UltravioletPhysical and Theoretical ChemistryUracilThymineCytosineThe Journal of Chemical Physics
researchProduct

OH-functionalized open-ended armchair single-wall carbon nanotubes (SWCNT) studied by density functional theory

2011

The structures of ideal armchair (5,5) single-wall carbon nanotubes (SWCNTs) of different lengths (3.7, 8.8, and 16.0 A for C40H20, C80H20, and C140H20) and with 1–10 hydroxyl groups at the end of the nanotube were fully optimized at the B3LYP/3-21G level, and in some cases at the B3LYP/6-31G* level, and the energy associated with the attachment of the OH substituent was determined. The OH-group attachment energy was compared with the OH functionalization of phenanthrene and picene models and with previous results for zigzag (9.0) SWCNT systems. In comparison to zigzag SWCNTs, the armchair form is more (by about 5 to 10 kcal mol−1) reactive toward hydroxylation. Figure The structures of ide…

NanotubeMaterials scienceSubstituentchemistry.chemical_elementCarbon nanotubeHydroxylationSpectrum Analysis RamanDFTHydroxylation energyCatalysislaw.inventionInorganic Chemistrychemistry.chemical_compoundlawComputational chemistryPhysical and Theoretical ChemistryArmchair SWCNTOriginal PaperHydroxyl RadicalNanotubes CarbonOH functionalizationOrganic ChemistryCarbonComputer Science ApplicationsCrystallographyModels ChemicalComputational Theory and MathematicschemistryPiceneZigzagSurface modificationDensity functional theoryEnd substitutionCarbonJournal of Molecular Modeling
researchProduct

Diaryl-dithiolanes and -isothiazoles: COX-1/COX-2 and 5-LOX-inhibitory, OH scavenging and anti-adhesive activities

2008

Three series of non-steroidal anti-inflammatory drugs (NSAIDs) inhibiting the cyclooxygenase/5-lipoxygenase (COX/5-LOX) pathways as such as formation of hydroxyl radicals and adhesion were prepared: 4,5-diaryl isothiazoles, 4,5-diaryl 3H-1,2-dithiole-3-thiones and 4,5-diaryl 3H-1,2-dithiole-3-ones. The aim of the present study was to develop substances which can intervene into the inflammatory processes via different mechanisms of action as multiple target non-steroidal anti-inflammatory drugs (MTNSAIDs) with increased anti-inflammatory potential. The current lead 11a was evaluated in COX-1/2, 5-LOX and (*)OH scavenging in vitro assays and in a static adhesion assay where it proved to inhib…

NeutrophilsClinical BiochemistryMacrophage-1 AntigenPharmaceutical SciencePeritonitisPharmacologyBiochemistryMiceIn vivoDrug DiscoveryCell AdhesionAnimalsCyclooxygenase InhibitorsLipoxygenase InhibitorsSulfhydryl CompoundsCell adhesionMolecular BiologybiologyHydroxyl RadicalChemistryAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryIn vitro toxicologyBiological activityFree Radical ScavengersAdhesionIn vitroThiazolesBiochemistryCyclooxygenase 2Arachidonate 5-lipoxygenaseCyclooxygenase 1biology.proteinMolecular MedicineCyclooxygenaseBioorganic & Medicinal Chemistry
researchProduct

Aging of biogenic secondary organic aerosol via gas-phase OH radical reactions

2012

The Multiple Chamber Aerosol Chemical Aging Study (MUCHACHAS) tested the hypothesis that hydroxyl radical (OH) aging significantly increases the concentration of first-generation biogenic secondary organic aerosol (SOA). OH is the dominant atmospheric oxidant, and MUCHACHAS employed environmental chambers of very different designs, using multiple OH sources to explore a range of chemical conditions and potential sources of systematic error. We isolated the effect of OH aging, confirming our hypothesis while observing corresponding changes in SOA properties. The mass increases are consistent with an existing gap between global SOA sources and those predicted in models, and can be described b…

OzoneFree Radicals010504 meteorology & atmospheric sciencesUltraviolet Rayschemistry.chemical_element010501 environmental sciencesMass spectrometrybehavioral disciplines and activities01 natural sciencesOxygenMass SpectrometryAtmospherechemistry.chemical_compoundOzoneOrganic Chemicals0105 earth and related environmental sciencesAerosolsMultidisciplinaryOzonolysisAtmosphereHydroxyl RadicalReproducibility of ResultsAerosolOxygenModels ChemicalchemistryAtmospheric chemistryEnvironmental chemistryPhysical SciencesSolventsHydroxyl radicalProceedings of the National Academy of Sciences of the United States of America
researchProduct

On the nature of macroradicals formed upon radiolysis of aqueous poly(N-vinylpyrrolidone) solutions

2020

In this work we have explored the nature of macroradicals formed upon radiolysis of aqueous poly(N-vinylpyrrolidone) (PVP) solutions using pulse radiolysis, density functional theory (DFT) and literature data. On the basis of literature data on site-specific kinetics of hydrogen abstraction from simple amides and spectra corresponding to specific radical sites on the same amides we have assessed the distribution of H-atom abstraction by `OH radicals from different positions on the pyrrolidone ring and the polymer backbone. Pulse radiolysis experiments performed at different doses per pulse and different PVP concentrations demonstrate that the H-abstracting radiolysis products are not quanti…

PULSE-RADIOLYSISMaterials sciencePulse radiolysisCROSS-LINKINGNanogelsMICROGELSPOLY(ACRYLIC ACID) NANOGELSHYDROXYL RADICALSPhotochemistry01 natural sciences030218 nuclear medicine & medical imaging03 medical and health scienceschemistry.chemical_compoundDELIVERYNanogel0302 clinical medicine0103 physical sciencesMacroradicalRadiationAqueous solution010308 nuclear & particles physicsN-VinylpyrrolidonePulse (physics)ELECTRONSNETWORKSchemistryRadiolysispoly(N-vinyl pyrrolidone)Density functional theoryDensity functional theoryMacroradicalsSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePOLYMERSRADIATION-INDUCED SYNTHESIS
researchProduct

2009

Abstract. The emission of nitric oxide (NO) by soils (SNOx) is an important source of oxides of nitrogen (NOx=NO+NO2) in the troposphere, with estimates ranging from 4 to 21 Tg of nitrogen per year. Previous studies have examined the influence of SNOx on ozone (O3) chemistry. We employ the ECHAM5/MESSy atmospheric chemistry model (EMAC) to go further in the reaction chain and investigate the influence of SNOx on lower tropospheric NOx, O3, peroxyacetyl nitrate (PAN), nitric acid (HNO3), the hydroxyl radical (OH) and the lifetime of methane (τCH4). We show that SNOx is responsible for a significant contribution to the NOx mixing ratio in many regions, especially in the tropics. Furthermore, …

Peroxyacetyl nitrateAtmospheric Sciencechemistry.chemical_compoundOzonechemistryAtmospheric chemistryEnvironmental chemistryMixing ratiochemistry.chemical_elementHydroxyl radicalNitrogenNOxTrace gasAtmospheric Chemistry and Physics
researchProduct

Photochemical and photobiological studies with acridine and phenanthridine hydroperoxides in cell-free DNA.

1997

The acridine and phenanthridine hydroperoxides 3 and 7 were synthesized as photochemical hydroxyl radical sources for oxidative DNA damage studies. The generation of hydroxyl radicals upon UVA irradiation (lambda = 350 nm) was verified by trapping experiments with 5,5-dimethyl-1-pyrroline N-oxide and benzene. The enzymatic assays of the damage in cell-free DNA from bacteriophage PM2 caused by the acridine and phenanthridine hydroperoxides 3 and 7 under near-UVA irradiation revealed a wide range of DNA modifications. Particularly, extensive single-strand break formation and DNA base modifications sensitive to formamidopyrimidine DNA glycosylase (Fpg protein) were observed. In the photooxidat…

PhenanthridineCell-Free SystemDNA damageDNA SuperhelicalHydroxyl RadicalPhotochemistryUltraviolet RaysRadicalGeneral MedicineFormamidopyrimidine DNA glycosylasePhotochemistryBiochemistryPhotoinduced electron transferPeroxidesCyclic N-Oxideschemistry.chemical_compoundchemistryAcridineHydroxyl radicalSpin LabelsPhysical and Theoretical ChemistryOxidation-ReductionDNADNA DamagePhotochemistry and photobiology
researchProduct

Calcium- and potassium-permeable plasma membrane transporters are activated by copper inArabidopsisroot tips: linking copper transport with cytosolic…

2012

Transition metals such as copper can interact with ascorbate or hydrogen peroxide to form highly reactive hydroxyl radicals (OH . ), with numerous implications to membrane transport activity and cell metabolism. So far, such interaction was described for extracellular (apoplastic) space but not cytosol. Here, a range of advanced electrophysiological and imaging techniques were applied to Arabidopsis thaliana plants differing in their copper-transport activity: Col-0, high-affinity copper transporter COPT1-overexpressing (C1 OE ) seedlings, and T-DNA COPT1 insertion mutant ( copt1 ). Low Cu concentrations (10 μ m) stimulated a dose-dependent Gd 3+ and verapamil sensitive net Ca 2+ influx in …

PhysiologyChemistryRadicalCopper toxicitychemistry.chemical_elementPlant ScienceMembrane transportmedicine.diseasePeroxideCopperCytosolchemistry.chemical_compoundBiochemistrymedicineBiophysicsHydroxyl radicalHydrogen peroxidePlant, Cell & Environment
researchProduct