Search results for "PHOTOCHEMISTRY"

showing 10 items of 2034 documents

Photoinduced dissociation of anionic and electron detachment of dianionic gold clusters by use of a laser pointer

2002

Abstract Size-selected anionic and dianionic gold clusters have been stored in a Penning trap and irradiated with the green light of a laser pointer. As examples of special interest, the systems Au 7 − and Au 29 2− have been chosen. In particular, Au 7 − , a small gold cluster with closed electron shell, is observed to decay into Au 6 − and Au 5 − with a decay pathway branching ratio similar to that of Au 9 + . The dianionic cluster Au 29 2− shows electron detachment upon photoexcitation. This observation is in agreement with independent experiments [Stoermer et al., Int. J. Mass Spectrom. 201 (2001) 63], where Au 29 2− is found to be the smallest dianion produced by neutral monomer evapora…

Gold clusterChemistryBranching fractionPhotodissociationElectron shellCondensed Matter PhysicsPenning trapPhotochemistryDissociation (chemistry)PhotoexcitationCluster (physics)Physical chemistryPhysical and Theoretical ChemistryInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
researchProduct

A Universal Approach to Quantify Overpotential-Dependent Selectivity Trends for the Competing Oxygen Evolution and Peroxide Formation Reactions : A C…

2021

In this article, we study the competing oxygen evolution and hydrogen peroxide (H2O2) formation reactions for periodic models of graphene with different active-site concentrations by means of densi...

GrapheneOxygen evolutionChemie02 engineering and technologyOverpotential010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesPeroxide3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundGeneral EnergychemistrylawElectrodePhysical and Theoretical Chemistry0210 nano-technologySelectivityHydrogen peroxide
researchProduct

Synthesis of 2,3‐Dihydro‐4‐pyridones, 4‐Quinolones, and 2,3‐Dihydro‐4‐azocinones by Visible‐Light Photocatalytic Aerobic Dehydrogenation

2019

Green chemistryChemistryOrganic Chemistry4-quinolonesPhotocatalysisDehydrogenationPhysical and Theoretical ChemistryVisible light photocatalyticPhotochemistryEuropean Journal of Organic Chemistry
researchProduct

Strain Release Chemistry of Photogenerated Small‐Ring Intermediates

2021

Abstract Photochemical processes, such as isomerizations and cycloadditions, have proven to be very useful in the construction of highly strained molecular frameworks. Photoinduced ring strain enables subsequent exergonic reactions which do not require the input of additional chemical energy and provides a variety of attractive synthetic options leading to complex structures. This review covers the progress achieved in the application of sequences combining excitation by ultraviolet light to form strained intermediates, which are further transformed to lower energy products in strain‐release reactions. As ring strain is considerable in small ring systems, photogenerated three‐ and four‐memb…

Green chemistryExergonic reactionphotochemistryStrain (chemistry)Chemistrygreen chemistryOrganic ChemistryReviewsGeneral ChemistryReviewstrain-releaseRing (chemistry)PhotochemistryCatalysisRing strainChemical energyPhotochemistry | Reviews Showcasering strainUltraviolet lighttransition-metal catalysisExcitationChemistry (Weinheim an Der Bergstrasse, Germany)
researchProduct

Frontispiece: Strain Release Chemistry of Photogenerated Small‐Ring Intermediates

2021

Green chemistryStrain (chemistry)ChemistryOrganic ChemistryGeneral ChemistryRing (chemistry)PhotochemistryCatalysisRing strainChemistry – A European Journal
researchProduct

Structural insight on organosilica electrodes for waste-free alcohol oxidations

2007

Organic modification of sol-gel catalytic glassy electrodes made of a thin layer of organosilica doped with nitroxyl radical TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) crucially enhances stability in the waste-free oxidation of alcohols to carbonyls in water. Structural comparison between analogous films made of organosilica and unmodified SiO2 shows that the origin of the pronounced stable activity of the ORMOSIL film lies in high hydrophobic and also in the pronounced low degree of hydrophilicity.

Green chemistryoxidationalcoholgreen chemistryInorganic chemistryAlcoholNitroxylGeneral ChemistryPhotochemistryHeterogeneous catalysisOrmosilCatalysisCatalysischemistry.chemical_compoundchemistryAlcohol oxidationsol-gelanodicTEMPOSol-gel
researchProduct

Are the five natural DNA/RNA base monomers a good choice from natural selection?

2009

In order to prevent the damaging effects of sun radiation in the genetic material, its constituent chromophores, the five natural DNA/RNA nucleobases cytosine, thymine, uracil, adenine, and guanine, should be able to efficiently dissipate absorbed radiation, UV specifically, avoiding as much as possible photoreactions leading to lesions. It has been established experimentally and theoretically that efficient internal conversion channels, still open and relevant in the oligomer-stacked strands, exist in the monomers allowing an effective waste of the initial energy. Previous evidences cannot explain, however, why minor differences in the molecular structure modify drastically the photochemis…

GuanineOrganic ChemistryUracilConical intersectionInternal conversion (chemistry)PhotochemistryCatalysisThymineNucleobasechemistry.chemical_compoundchemistryExcited statePhysical and Theoretical ChemistryCytosineJournal of Photochemistry and Photobiology C: Photochemistry Reviews
researchProduct

Modelling Photoionisations in Tautomeric DNA Nucleobase Derivatives 7H-Adenine and 7H-Guanine: Ultrafast Decay and Photostability

2021

The study of radiation effects in DNA is a multidisciplinary endeavour, connecting the physical, chemical and biological sciences. Despite being mostly filtered by the ozone layer, sunlight radiation is still expected to (photo)ionise DNA in sizeable yields, triggering an electron removal process and the formation of potentially reactive cationic species. In this manuscript, photoionisation decay channels of important DNA tautomeric derivatives, 7H-adenine and 7H-guanine, are characterised with accurate CASSCF/XMS-CASPT2 theoretical methods. These simulation techniques place the onset of ionisation for 7H-adenine and 7H-guanine on average at 8.98 and 8.43 eV, in line with recorded experimen…

Guaninephotoionisation010402 general chemistryPhotochemistryphotostability01 natural sciencesNucleobasechemistry.chemical_compoundUltraviolet visible spectroscopy0103 physical sciencesUV/Vis spectroscopyexcited states010304 chemical physicsconical intersectionsCationic polymerizationionisation potentialsEspectroscòpia infrarojaQuímicaConical intersectionTautomer0104 chemical scienceschemistryExcited stateCASSCF/CASPT2DNA/RNAGround statePhotochem
researchProduct

A Chemosensor Bearing Sulfonyl Azide Moieties for Selective Chromo-Fluorogenic Hydrogen Sulfide Recognition in Aqueous Media and in Living Cells

2014

A simple chemodosimeter based on a sulfonyl azide dye (1-Az), which displayed a highly selective response toward hydrogen sulfide anion in mixed aqueous media, was synthesised and characterised. Addition of hydrogen sulfide to acetonitrile/HEPES 1:1 solutions of 1-Az induced a clear colour change from red-orange to yellow, which was easily detected by the naked eye, and by an enhancement in the emission intensity. Other common anions, thiol-containing biomolecules and oxidants did not induce any noticeable colour or fluorescence modulation in the probe. The chemodosimeter also showed a good sensitivity, with limits of detection of 11.91 and 0.63 μM by using UV/Vis or fluorescence measuremen…

HEPESSulfonylchemistry.chemical_classificationHydrogen sulfideOrganic Chemistrychemistry.chemical_elementPhotochemistryFluorescenceSulfurchemistry.chemical_compoundchemistryAzideNaked eyePhysical and Theoretical ChemistryAcetonitrileEuropean Journal of Organic Chemistry
researchProduct

The new era of 1,2,4-oxadiazoles

2009

The synthesis, the chemical and photochemical reactivity, and the use of 1,2,4-oxadiazoles in materials and as bioactive compounds have been reviewed. The material in this survey includes some historical background, general features, state-of-the-art applications together with a critical discussion about current limitations and suggestions for future developments.

HETEROCYCLES OXADIAZOLES BIOACTIVE COMPOUNDS PHOTOCHEMISTRY FIVE-MEMBERED HETEROAROMATICSChemistryOrganic ChemistryNanotechnologyPhotochemical reactivitySettore CHIM/06 - Chimica OrganicaPhysical and Theoretical ChemistryBiochemistryCritical discussion
researchProduct