Search results for "PHOTOCHEMISTRY"

showing 10 items of 2034 documents

Fluorescence emission and enhanced photochemical stability of Zn(II)-5-triethyl ammonium methyl salicylidene ortho-phenylendiiminate interacting with…

2010

Abstract The photophysical and photochemical properties of the cationic Zn II complex of 5-triethyl ammonium methyl salicylidene ortho-phenylendiimine (ZnL 2+ ) interacting with native DNA were investigated by steady state and time-resolved fluorescence spectroscopies. Experimental results indicate that, in the presence of DNA, ZnL 2+ is efficiently protected from a photochemical process, which occurs when it is in the free state dispersed in aqueous solution. The analysis of the absorption and emission spectra of ZnL 2+ , both stored in the dark and after exposure to tungsten lamp light for 24 h, corroborated by quantum chemical calculations, allowed us to point out that ZnL 2+ undergoes a…

Intercalation (chemistry)Context (language use)PhotochemistryBiochemistryFluorescence spectroscopyFluorescenceInorganic ChemistrySchiff baseIntercalationOrganometallic CompoundsMoleculeFluorescence spectroscopyPhotooxidationSettore CHIM/02 - Chimica FisicaAqueous solutionChemistrySpectrum AnalysisDNAPhotochemical ProcessesFluorescenceIntercalating AgentsSolventZincSettore CHIM/03 - Chimica Generale E InorganicaSolventsSteady state (chemistry)Oxidation-ReductionJournal of inorganic biochemistry
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Electrochemically Induced Reversible and Irreversible Coupling of Triarylamines

2011

The electrochemical coupling and dimerization behavior of the low molecular compounds triphenylamine (TPA) and 9-phenylcarbazole (PHC) in comparison to tri-p-tolylamine (p-TTA) with para-blocked methyl groups has been investigated in detail. In contrast to the unsubstituted radical cations of TPA and PHC, the radical cations of p-TTA are stable in the radical cation state and do not undergo any further coupling reactions. However, we found that the dicationic state of p-TTA does undergo two different competitive reaction pathways: (1) an irreversible intramolecular coupling reaction which leads to phenylcarbazole moieties and (2) a reversible intermolecular dimerization leading to charged σ…

Intermolecular forcePhotochemistryTriphenylamineElectrochemistryCoupling reactionSurfaces Coatings and FilmsCoupling (electronics)chemistry.chemical_compoundMonomerchemistryRadical ionIntramolecular forceMaterials ChemistryPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Intersystem Crossing and Light-Induced Bistability in Iron(?) Spin-Crossover Compounds

1996

Abstract The dynamics of the high-spin→low-spin intersystem crossing process in iron(?) spin-crossover compounds are strongly influenced by cooperative effects of elastic origin which are due to the large difference in volume between high-spin and low-spin complexes. The deviation from first order kinetics is attributed to a build-up of an internal pressure as the relaxation proceeds, leading to a characteristic self-acceleration. The elastic interactions may lead to a light-induced bistability for systems which otherwise remain in the high-spin state down to cryogenic temperatures.

Intersystem crossingBistabilityChemical physicsChemistrySpin crossoverRelaxation (NMR)Light inducedInternal pressureCondensed Matter::Strongly Correlated ElectronsRate equationCondensed Matter PhysicsInternal conversion (chemistry)PhotochemistryMolecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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Corrigendum: An Unusually Small Singlet-Triplet Gap in a Quinoidal 1,6-Methano[10]annulene Resulting from Baird's 4n π-Electron Triplet Stabilization.

2016

Within the continuum of π-extended quinoidal electronic structures exist molecules that by design can support open-shell diradical structures. The prevailing molecular design criteria for such structures involve proaromatic nature that evolves aromaticity in open-shell diradical resonance structures. A new diradical species built upon a quinoidal methano[10]annulene unit is synthesized and spectroscopically evaluated. The requisite intersystem crossing in the open-shell structure is accompanied by structural reorganization from a contorted Mobius aromatic-like shape in S0 to a more planar shape in the Huckel aromatic-like T1. This stability was attributed to Baird’s Rule which dictates the …

Intersystem crossingDiradicalChemical physicsChemistryExcited stateMoleculeAromaticityGeneral ChemistryElectronSinglet stateAnnulenePhotochemistryCatalysisAngewandte Chemie (International ed. in English)
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Heterocyclic photorearrangements. Photoinduced rearrangement of 3-styryl-1,2,4-oxadiazoles

1990

The photochemical behaviour of 3-styryl-5-phenyl-(5-methyl)-1,2,4-oxadiazoles in methanol at 254 nm has been investigated. A photoinduced rearrangement to the quinoline system has been pointed out and explained as proceeding through an initial photolysis of the ring ON bond, followed by a six membered ring closure reaction involving the styryl moiety.

Intramolecular reactionBicyclic moleculemedicine.drug_classOrganic ChemistryQuinolinePhotodissociationCarboxamideRing (chemistry)PhotochemistryCis trans isomerizationchemistry.chemical_compoundchemistrymedicineMoietyJournal of Heterocyclic Chemistry
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Gas-phase ion chemistry of protonated melatonin

2009

The gas-phase ion chemistry of protonated melatonin has been investigated by mass spectrometric (MS) techniques involving chemical ionisation, fast atom bombardment and electrospray ionisation. Either naturally-occurring or collision-induced decomposition experiments have been carried out using side chain tetra-deuterium-labelled derivatives, as well as the corresponding N–D derivatives obtained by exchange with D2O. The analysis of experimental results allows definite pathways for the formation of the ion at m/z 174 to be assigned and sheds some more light on the overall fragmentation pathways. Experiments on labelled derivatives evidenced H–D scrambling processes during fragmentation.

IonsElectrospraySpectrometry Mass Electrospray IonizationChemistryElectrospray ionizationInorganic chemistryDeuterium Exchange MeasurementProtonationmelatonin ESI/MS ESI/MS/MSion chemistryGeneral MedicineFast atom bombardmentPhotochemistryAtomic and Molecular Physics and OpticsIonFragmentation (mass spectrometry)AmmoniaTandem Mass SpectrometryAcetamidesProton affinityQuantum TheoryGasesProtonsSpectroscopyGas-phase ion chemistryMelatonin
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Dynamics of closure of zinc bis-porphyrin molecular tweezers with copper(II) ions and electron transfer.

2011

Zinc bis-porphyrin molecular tweezers composed of a N(4) spacer bound through pyridyl units to the meso position of porphyrins were synthesized, and the tweezers are closed by the coordination of a copper(II) ion inside the spacer ligand. The effect of the π-π interaction between the porphyrin rings in the closed conformation on the absorption spectra of multi-electron oxidized species and the reduction potentials were clarified by chemical and electrochemical oxidation of the closed form of the zinc bis-porphyrin molecular tweezers in comparison with the open form without copper(II) ion and the corresponding porphyrin monomer. The shifts in redox potentials and absorption spectrum of the p…

IonsLigandMetalloporphyrinsOrganic Chemistrychemistry.chemical_elementGeneral ChemistryZincElectrochemical TechniquesPhotochemistryPorphyrinCopperCatalysisDicationElectron TransportElectron transferchemistry.chemical_compoundchemistryTweezerspolycyclic compoundsheterocyclic compoundsSpectrophotometry UltravioletMolecular tweezersOxidation-ReductionCopperChemistry (Weinheim an der Bergstrasse, Germany)
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Ion pair recognition receptor based on an unsymmetrically 1,1'-disubstituted ferrocene-triazole derivative.

2012

The ferrocene-triazole derivative 4, available from 1,1'-bis(diazido)ferrocene by sequential functionalization through click-type chemistry and the Staudinger reaction, is elaborated as a lab-on-a-molecule for the selective sensing of HP(2)O(7)(3-) and Hg(2+). Receptor 4 behaves as a ratiometric fluorescent probe for HP(2)O(7)(3-) with a good selectivity over other anions, whereas in the presence of Hg(2+) it modifies the fluorescent emission of the pyrene unit, acting as a selective on-off fluorescent sensor for Hg(2+) with a low detection limit. The most salient feature of compound 4 is its behavior as an excellent electrooptical ion pair recognition receptor able to simultaneously recogn…

IonsMagnetic Resonance SpectroscopyMetallocenesOrganic ChemistryTriazolesPhotochemistryFluorescenceRedoxIonchemistry.chemical_compoundchemistryFerroceneElectrochemistryPyreneSpectrophotometry UltravioletStaudinger reactionFerrous CompoundsSelectivityDerivative (chemistry)Fluorescent DyesThe Journal of organic chemistry
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Bright Blue Phosphorescence from Cationic Bis-Cyclometalated Iridium(III) Isocyanide Complexes

2012

We report new bis-cyclometalated cationic indium(III) complexes [((CN)-N-boolean AND)(2)Ir(CN-tert-Bu)(2)](CF3SO3) that have tert-butyl isocyanides as neutral auxiliary ligands and 2-phenylpyridine or 2-(4'-fluoropheny1)-R-pyridines (where R is 4-methoxy, 4-tert-butyl, or 5-trifluoromethyl) as (CN)-N-boolean AND ligands. The complexes are white or pale yellow solids that show irreversible reduction and oxidation processes and have a large electrochemical gap of 3.58-3.83 V. They emit blue or bluegreen phosphorescence in liquid/solid solutions from a cyclometalating-ligand-centered excited state. Their emission spectra show vibronic structure with the highest-energy luminescence peak at 440-…

Ir(Iii) ComplexesIsocyanideCationic polymerizationchemistry.chemical_elementEmitting Electrochemical-CellsExcited-State PropertiesElectroluminescent DevicesPhotochemistryAncillary LigandsInorganic Chemistrychemistry.chemical_compoundchemistryExcited stateEfficient BlueIii ComplexesMetal-ComplexesEmission spectrumIridiumPhysical and Theoretical ChemistryPhosphorescenceLuminescenceTurn-On TimesPhotophysical PropertiesSolid solutionInorganic Chemistry
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Intramolecular electron transfer between molybdenum and iron mimicking bacterial sulphite dehydrogenase

2014

Diferrocenyl/diferrocenium substituted dioxido molybdenum(VI) complexes [Fe2MoO2] 2(Fc)/[2(FC)]²⁺ mimic the catalytic active site including the redox subunits as well as the catalytic function of bacterial sulphite oxidases.

IronSulfite DehydrogenaseMolecular Conformationchemistry.chemical_elementBiocompatible MaterialsElectronsCrystallography X-RayPhotochemistryRedoxCatalysisCatalysisElectron TransportElectron transferCoordination ComplexesCatalytic DomainPolymer chemistryMaterials ChemistrySulfite dehydrogenaseFerrous CompoundsMolybdenumBacteriabiologyMetals and AlloysActive siteGeneral ChemistryElectron transport chainSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryMolybdenumIntramolecular forceCeramics and Compositesbiology.proteinOxidation-ReductionChemical Communications
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