Search results for "Photochemistry"

showing 10 items of 2034 documents

Theoretical study on the decomposition mechanism of bisphenol A polycarbonate induced by the combined effect of humidity and UV irradiation.

2020

Polycarbonate (PC) is a good material for covering and protecting cultural heritage sites because of its durability, mechanical properties, and transparency. When bisphenol A polycarbonate is subjected to weathering conditions this polymer shows several degradation processes depending on the irradiation wavelength, humidity and temperature. In particular, the combined effects of humidity and UV irradiation speed up the PC molecular weight reduction. In this work, the decomposition mechanisms associated to the hydrolysis process are scrutinized and the effects of UV irradiation on the hydrolysis process are evaluated throughout the Density Functional Theory (DFT) approach. It was found that …

010407 polymersMaterials sciencePolymersUltraviolet Rays02 engineering and technologyPhotochemistry01 natural sciencesHydrolysisDFT modeling; hydrolysis process; polycarbonate; weathering degradationMaterials ChemistryIrradiationPhysical and Theoretical ChemistryPolycarbonateBenzhydryl CompoundsSpectroscopychemistry.chemical_classificationHumidityHumidityPolymerModels Theoretical021001 nanoscience & nanotechnologyComputer Graphics and Computer-Aided DesignDecomposition0104 chemical sciencespolycarbonatechemistryhydrolysis processvisual_artvisual_art.visual_art_mediumDegradation (geology)Density functional theoryDFT modeling0210 nano-technologyweathering degradationJournal of molecular graphicsmodelling
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Molecular composition of dissolved organic matter from a wetland plant (Juncus effusus) after photochemical and microbial decomposition (1.25 yr): Co…

2013

We hypothesized that microbial and photochemical processing of dissolved organic matter (DOM) determines its molecular formula composition in aquatic systems to a greater degree than does the original source of the DOM. To test this hypothesis, we exposed DOM from a leachate of a wetland plant (Juncus effusus) to solar radiation or incubated it in the dark for 1.25 yr. Analysis of the extracted DOM of the leachates via Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) identified 2800 molecular formulae. Of the formulae in the initial DOM, 11% were lost during microbial decomposition in the dark and 54% under solar radiation. Solar radiation also produced a large number…

0106 biological sciences010504 meteorology & atmospheric sciencesbiologyChemistry010604 marine biology & hydrobiologyAquatic ecosystemta1171biology.organism_classificationPhotochemistry01 natural sciencesDecompositionDeep seaWater columnGeochemistry and PetrologyEnvironmental chemistryJuncusDissolved organic carbonBotany14. Life underwaterLeachateMicrobial biodegradation0105 earth and related environmental sciences
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Monitoring of transglutaminase crosslinking reaction by 1H NMR spectroscopy on model substrates

2015

International audience; A new method based on 1H NMR spectroscopy was developed for monitoring transglutaminase crosslinking reaction with model molecules (CBZ-Gln-Gly and N-α-acetyl-lysine). The transglutaminase reaction led to the appearance of new resonances on NMR spectrum as well as significant decrease in others. The new observed resonances, originated from newly formed ɛ-(γ-glutamyl)lysine isopeptide bonds, evidence the enzymatic reaction and allow to quantify the ɛ-(γ-glutamyl)lysine fragment. Moreover, the decrease in resonance intensity, originated from lysine, permit to determine the crosslinking degree. These results obtained by 1H NMR spectroscopy can be used as an alternative …

0106 biological sciences1h nmr spectroscopyTissue transglutaminaseLysineCrosslinking degreePhotochemistrycomplex mixtures01 natural sciences03 medical and health sciencesModel substratesɛ-(γ-glutamyl)-lysineColloid and Surface ChemistryLiquid chromatography–mass spectrometry010608 biotechnologyOrganic chemistryMolecule[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology030304 developmental biologyAlternative methods0303 health sciencesbiologyChemistryResonanceNuclear magnetic resonance spectroscopyMicrobial transglutaminasebiology.proteinColloids and Surfaces A: Physicochemical and Engineering Aspects
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Functional rearrangement of the light-harvesting antenna upon state transitions in a green alga

2014

AbstractState transitions in the green alga Chlamydomonas reinhardtii serve to balance excitation energy transfer to photosystem I (PSI) and to photosystem II (PSII) and possibly play a role as a photoprotective mechanism. Thus, light-harvesting complex II (LHCII) can switch between the photosystems consequently transferring more excitation energy to PSII (state 1) or to PSI (state 2) or can end up in LHCII-only domains. In this study, low-temperature (77 K) steady-state and time-resolved fluorescence measured on intact cells of Chlamydomonas reinhardtii shows that independently of the state excitation energy transfer from LHCII to PSI or to PSII occurs on two main timescales of <15 ps and …

0106 biological sciencesPhotosystem IIEnergy transferBiophysicsLight-Harvesting Protein ComplexesphotosystemChlamydomonas reinhardtiiPhotosystem IPhotochemistry01 natural sciences03 medical and health sciencesstate transitionsgreen algaSDG 7 - Affordable and Clean Energy030304 developmental biologyPhotosystem0303 health sciencesenergy transfer/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energybiologyPhotosystem I Protein ComplexChemistryta1182Photosystem II Protein ComplexState (functional analysis)biology.organism_classificationFluorescenceCell BiophysicsAtomic physicsExcitationChlamydomonas reinhardtii010606 plant biology & botanyBiophysical journal
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Selective photocatalytic oxidation of aromatic alcohols in water by using P-doped g-C3N4

2018

A set of bare and P-doped graphitic carbon nitride (g-C3N4) photocatalysts has been prepared by thermal condensation of melamine, urea or thiourea. For the sake of comparison, a g-C3N4 sample obtained in the presence of cyanuric acid and thermally exfoliated C3N4 powders were also studied. The materials were physicochemically characterized and their photocatalytic activity was studied for the selective oxidation of benzyl alcohol (BA), 4-methoxy benzyl alcohol (4-MBA) and piperonyl alcohol (PA) in water suspension both under UV and visible light irradiation. The influence of the type and position of the substituents on conversion and selectivity to aldehyde was remarkable. The presence of P…

02 engineering and technology010402 general chemistryPhotochemistryAromatic alcohols01 natural sciencesAldehydeCatalysisCatalysichemistry.chemical_compoundPhotocatalysiAromatic alcoholPhotocatalysisG-C3N4General Environmental ScienceDoped carbon nitridechemistry.chemical_classification2300ChemistryProcess Chemistry and TechnologyGraphitic carbon nitride021001 nanoscience & nanotechnology0104 chemical sciencesThioureaBenzyl alcoholPhotocatalysisSelective oxidationSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyMelamineCyanuric acidSelectivityNuclear chemistryApplied Catalysis B: Environmental
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Microscopic Revelation of Charge-Trapping Sites in Polymeric Carbon Nitrides for Enhanced Photocatalytic Activity by Correlating with Chemical and El…

2019

The influences of chemical and electronic structures on the photophysical properties of polymeric carbon nitrides (PCNs) photocatalysts, which govern the microscopic mechanisms of the superior photocatalytic activity under visible-light irradiation, have been resolved in this work. Time-resolved photoluminescence and in situ electron paramagnetic resonance measurements indicate that the photoexcited electrons in the fractured PCNs swiftly transfer to the C2p-localized states where the trapped photoelectrons exhibit longer lifetime compared to those in the ordinary PCNs. Moreover, the structure deviation at the carbon (Cb) atoms around the bridging sites of heptazine ring units, where trappe…

021110 strategic defence & security studiesMaterials sciencePhotoluminescenceHeptazineHydrogen bond0211 other engineering and technologiesDFT calculation02 engineering and technologyElectronPhotoelectric effect021001 nanoscience & nanotechnologyPhotochemistrylaw.inventionpolymeric carbon nitridechemistry.chemical_compoundchemistrylawSSNMR spectroscopyPhotocatalysisGeneral Materials ScienceDensity functional theoryvisible-light-driven photocatalyst0210 nano-technologyElectron paramagnetic resonanceEPR spectroscopyACS Applied Materials &amp; Interfaces
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Formation of 2-nitrophenol from salicylaldehyde as a suitable test for low peroxynitrite fluxes

2016

There has been some dispute regarding reaction products formed at physiological peroxynitrite fluxes in the nanomolar range with phenolic molecules, when used to predict the behavior of protein-bound aromatic amino acids like tyrosine. Previous data showed that at nanomolar fluxes of peroxynitrite, nitration of these phenolic compounds was outcompeted by dimerization (e.g. biphenols or dityrosine). Using 3-morpholino sydnonimine (Sin-1), we created low fluxes of peroxynitrite in our reaction set-up to demonstrate that salicylaldehyde displays unique features in the detection of physiological fluxes of peroxynitrite, yielding detectable nitration but only minor dimerization products. By mean…

0301 basic medicineClinical BiochemistryPhotochemistryBiochemistryAdductNitrophenols03 medical and health scienceschemistry.chemical_compoundddc:570NitrationPeroxynitrous AcidAromatic amino acidsLeukocytesOrganic chemistryMoleculeHumansTyrosinelcsh:QH301-705.5Chromatography High Pressure Liquidlcsh:R5-920AldehydesMolecular StructureOrganic ChemistryPeroxynitrous acid030104 developmental biologylcsh:Biology (General)chemistrySalicylaldehydelcsh:Medicine (General)PeroxynitriteResearch PaperRedox Biology
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Singlet Oxygen Attack on Guanine: Reactivity and Structural Signature within the B-DNA Helix

2016

International audience; Oxidatively generated DNA lesions are numerous and versatile, and have been the subject of intensive research since the discovery of 8-oxoguanine in 1984. Even for this prototypical lesion, the precise mechanism of formation remains elusive due to the inherent difficulties in characterizing high-energy intermediates. We have probed the stability of the guanine endoperoxide in B-DNA as a key intermediate and determined a unique activation free energy of around 6 kcal mol−1 for the formation of the first C−O covalent bond upon the attack of singlet molecular oxygen (1O2) on the central guanine of a solvated 13 base-pair poly(dG-dC), described by means of quantum mechan…

0301 basic medicineGuanineBase pairGuanineMolecular Dynamics Simulation010402 general chemistryPhotochemistry01 natural sciencesCatalysis03 medical and health sciencesMolecular dynamicschemistry.chemical_compoundPolydeoxyribonucleotidesReactivity (chemistry)Base PairingSinglet OxygenChemistrySinglet oxygenOrganic ChemistrySolvationGeneral Chemistry0104 chemical sciences030104 developmental biologyCovalent bondHelixDNA B-FormOxidation-Reduction[CHIM.RADIO]Chemical Sciences/Radiochemistry
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Redox-Active Ferrocene grafted on H-Terminated Si(111): Electrochemical Characterization of the Charge Transport Mechanism and Dynamics

2019

AbstractElectroactive self-assembled monolayers (SAMs) bearing a ferrocene (Fc) redox couple were chemically assembled on H-terminated semiconducting degenerate-doped n-type Si(111) substrate. This allows to create a Si(111)|organic-spacer|Fc hybrid interface, where the ferrocene moiety is covalently immobilized on the silicon, via two alkyl molecular spacers of different length. Organic monolayer formation was probed by Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS) and X-ray photoelectron spectroscopy (XPS) measurements, which were also used to estimate thickness and surface assembled monolayer (SAM) surface coverage. Atomic force microscopy (AFM) measurements all…

0301 basic medicineMaterials for devicesMaterials sciencelcsh:Medicine-Surface engineeringPhotochemistryRedoxArticle03 medical and health scienceschemistry.chemical_compoundElectron transfer0302 clinical medicineX-ray photoelectron spectroscopyMonolayerSi(111); Charge Transport Mechanism and Dynamicslcsh:ScienceAlkylchemistry.chemical_classificationMultidisciplinarylcsh:RChemistry030104 developmental biologychemistryFerrocenelcsh:QCyclic voltammetry030217 neurology & neurosurgery
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Stable radical anions generated from a porous perylenediimide metal-organic framework for boosting near-infrared photothermal conversion

2019

Radical anions of electron-deficient systems are widely used, but are easily reoxidized upon exposure to air. Therefore, the stabilization of radical anions under ambient conditions is of great significance, but still remains a scientific challenge. Herein, perylenediimide is employed to prepare a crystalline metal-organic framework for stabilizing radical anions without extensive chemical modification. The porous, three-dimensional framework of perylenediimide can trap electron donors such as amine vapors and produce radical anions in-situ through photo-induced electron transfer. The radical anions are protected against quenching by shielding effect in air and remain unobstructed in air fo…

0301 basic medicineMultidisciplinaryMaterials scienceScienceQNear-infrared spectroscopyGeneral Physics and AstronomyChemical modification02 engineering and technologyGeneral ChemistryPhotothermal therapy021001 nanoscience & nanotechnologyPhotochemistryArticleGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesElectron transfer030104 developmental biologyShielding effectMetal-organic frameworkAmine gas treatinglcsh:Q0210 nano-technologyPorositylcsh:ScienceNature Communications
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