Search results for "electron transfer"

showing 10 items of 282 documents

Donor-acceptor substituted polyenes : orientation in mono- and multilayers

1992

Large molecules containing different chemical units whose interactions within the molecule result in new macroscopically observable effects, have become increasingly important.The organization of molecules of this type in ordered structures leads to functional molecular materials.Their use in molecular electronics requires that the units exhibit specific electronic properties. Recently, we reported on the intramolecular energy transfer through terminally substituted conjugated polyenes. An intramolecular electron transfer within donor-acceptor substituted polyenes can be achieved by introducing suitable terminal groups.

ChemistryPolyene SubstitutionsreaktionMechanical EngineeringMolecular electronicsNonlinear opticsConjugated systemPolyene540Orientation (vector space)Electron transferchemistry.chemical_compoundCrystallographyMechanics of MaterialsComputational chemistryIntramolecular forceMoleculeGeneral Materials Science
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Long lived photoinduced charges in donor-acceptor anthraquinone substituted thiophene copolymers

2006

The photoinduced charge-transfer properties of a series of polyalkylthiophene copolymers, carrying anthraquinone substituents covalently linked to the conjugated backbone, have been studied in the solid state by photoinduced absorption (PA) and light-induced electron spin resonance (LESR) spectroscopy. The measurements indicate the formation of metastable charges arising from the photoinduced electron transfer from the polythiophene backbone to the anthraquinone moieties. At low temperatures (below 200 K), long-lived persistent charges are formed, exhibiting lifetimes that extend for several minutes; their recombination kinetics has been studied by following the formation and decay of the P…

ChemistrySettore CHIM/06 - Chimica OrganicaConjugated systemPhotochemistryAcceptorAnthraquinonePhotoinduced electron transferSurfaces Coatings and Filmslaw.inventionPhotoexcitationchemistry.chemical_compoundlawMaterials ChemistryThiopheneconjugated polymersPolythiophenePhysical and Theoretical ChemistryElectron paramagnetic resonancephotophysics
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Ferrocenyl-functionalized tetranuclear gold(I) and gold(I)-copper(I) complexes based on tridentate phosphanes

2013

Tetranuclear AuI–FeII dimetallic and AuI–CuI–FeII trimetallic complexes bearing ferrocenyl (Fc) groups have been assembled by using two triphosphane ligands, namely, (PPh2CH2)2PPh (dpmp) and (PPh2)3CH (tppm). The compositions and structural type of the clusters are dependent on the stereochemistry of the P donor ligands. The complexes [tppmAu3Cu(C2R)3]PF6 [R = Fc (1) and 4-C6H4-Fc (2)] adopt a trigonal pyramidal {Au3Cu} arrangement of the coordinating metal core, whereas for the compounds with the linear triphosphane [Au4(dpmp)2(C2R)2](PF6)2 [R = Fc (3) and 4-C6H4-Fc (4)], a planar rhomboidal {Au4} framework was found. Clusters 1–4 were characterized by NMR spectroscopy and ESI-MS measureme…

ChemistryStereochemistrychemistry.chemical_elementTrigonal pyramidal molecular geometryNuclear magnetic resonance spectroscopyElectrochemistryRedoxCopperInorganic ChemistryMetalElectron transferchemistry.chemical_compoundCrystallographyTriphosphanevisual_artvisual_art.visual_art_mediumta116European journal of inorganic chemistry
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Probing DNA conductivity with photoinduced electron transfer and scanning tunneling microscopy.

2012

Abstract The possibility that the stacked DNA bases can mediate vectorial electron transfer has been examined using two different approaches. Experiments on photoinduced electron transfer with intercalated donors and acceptors (either randomly bound or linked dyads of ruthenium complex and viologen) indicate that while DNA may be a better medium than acetonitrile for electron transfer over short distances (2-3-base pair, equivalent to 10-14Å centre-to-centre separation), it is a poor medium for transport over larger separations. Attempts to measure conductivity of individual DNA molecules using scanning tunneling microscopy to image mixed monolayers of mercaptohexanol (MCH) and 30-mer or 10…

ChemistryViologenElectronsGeneral MedicineDNAPhotochemistryElectron transport chainPhotoinduced electron transferIntercalating Agentslaw.inventionElectron TransportElectron transferStructural BiologylawMicroscopy Scanning TunnelingMonolayerMicroscopymedicineNative stateScanning tunneling microscopeMolecular BiologyOxidation-Reductionmedicine.drugJournal of biomolecular structuredynamics
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Photoinduced ultrafast dye-to-semiconductor electron injection from nonthermalized and thermalized donor states.

2001

Electron injection from the transition metal complex Ru(dcbpy)(2)(NCS)(2) (dcbpy = 4,4'-dicarboxy-2,2'-bipyridine) into a titanium dioxide nanocrystalline film occurs on the femto- and picosecond time scales. Here we show that the dominating part of the electron transfer proceeds extremely rapidly from the initially populated, vibronically nonthermalized, singlet excited state, prior to electronic and nuclear relaxation of the molecule. The results are especially relevant to the understanding and design of molecular-based photovoltaic devices and artificial photosynthetic assemblies.

Chemistrybusiness.industryGeneral ChemistryElectronic structurePhotochemistryBiochemistryCatalysisNanocrystalline materialElectron transferColloid and Surface ChemistrySemiconductorTransition metalPicosecondExcited stateSinglet stateAtomic physicsbusinessJournal of the American Chemical Society
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Pigment−Pigment and Pigment−Protein Interactions in Recombinant Water-Soluble Chlorophyll Proteins (WSCP) from Cauliflower

2007

Plants contain water-soluble chlorophyll-binding proteins (WSCPs) that function neither as antennas nor as components of light-induced electron transfer of photosynthesis but are likely constituents of regulatory protective pathways in particular under stress conditions. This study presents results on the spectroscopic properties of recombinant WSCP from cauliflower reconstituted with chlorophyll b (Chl b) alone or with mixtures of Chl a and Chl b. Two types of experiments were performed: (a) measurements of stationary absorption spectra at 77 and 298 K and CD spectra at 298 K and (b) monitoring of laser flash-induced transient absorption changes with a resolution of 200 fs in the time doma…

Chlorophyll bCircular dichroismAbsorption spectroscopyCircular DichroismLasersDimerKineticsLight-Harvesting Protein ComplexesBrassicaPigments BiologicalRecombinant ProteinsSurfaces Coatings and FilmsKineticschemistry.chemical_compoundCrystallographyElectron transferchemistryUltrafast laser spectroscopyChlorinMaterials ChemistryLinear Energy TransferSpectrophotometry UltravioletPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Light-harvesting chlorophyll protein (LHCII) drives electron transfer in semiconductor nanocrystals

2017

Type-II quantum dots (QDs) are capable of light-driven charge separation between their core and the shell structures; however, their light absorption is limited in the longer-wavelength range. Biological light-harvesting complex II (LHCII) efficiently absorbs in the blue and red spectral domains. Therefore, hybrid complexes of these two structures may be promising candidates for photovoltaic applications. Previous measurements had shown that LHCII bound to QD can transfer its excitation energy to the latter, as indicated by the fluorescence emissions of LHCII and QD being quenched and sensitized, respectively. In the presence of methyl viologen (MV), both fluorescence emissions are quenched…

ChlorophyllParaquatPhotosynthetic reaction centreMaterials scienceAbsorption spectroscopyLight-Harvesting Protein ComplexesBiophysics02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesBiochemistryElectron TransportLight-harvesting complexElectron transferQuantum DotsUltrafast laser spectroscopyFluorescence Resonance Energy TransferAction spectrumPeasPhotosystem II Protein ComplexCell Biology021001 nanoscience & nanotechnologyFluorescence0104 chemical sciencesSemiconductorsQuantum dotNanoparticles0210 nano-technologyBiochimica et Biophysica Acta (BBA) - Bioenergetics
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Titelbild: Luminescence and Light‐Driven Energy and Electron Transfer from an Exceptionally Long‐Lived Excited State of a Non‐Innocent Chromium(III) …

2019

ChromiumElectron transferMaterials sciencechemistryExcited stateLight drivenchemistry.chemical_elementCover (algebra)General MedicineAtomic physicsLuminescenceAngewandte Chemie
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Tuning of the photoinduced charge transfer process in donor-acceptor "double cable" copolymers

2003

The covalent linking of acceptor molecules to electron donating conjugated polymer is an approach for the development of new photoactive materials for the fabrication of organic photoelectric conversion devices. With this strategy we have designed a polyalkylthiophene copolymer series containing in the side chain anthraquinone molecules as electron acceptor. The peculiar features of the copolymers are the good processability and the ease in tailoring the content of acceptor moieties. Their potential use as photoactive materials is investigated in terms of the photoinduced charge transfer properties, studied by FTIR photoinduced absorption and Light Induced Electron Spin Resonance spectrosco…

Condensed Matter PhysicConjugated systemPhotochemistryAnthraquinonePhotoinduced electron transferlaw.inventionchemistry.chemical_compoundlawMaterials ChemistryMoleculeDonor-acceptor alkylthiophene copolymerPhotoinduced charge transferElectron paramagnetic resonanceMechanical EngineeringElectronic Optical and Magnetic MaterialMetals and AlloysSettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsAcceptorElectronic Optical and Magnetic MaterialschemistryMechanics of MaterialsCovalent bondPolythiopheneLight-induced electron spin resonancePhotoinduced absorption
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Photoelectron spectroscopy of thin discontinuous metal films deposited onto a sapphire substrate

1995

Abstract The charging of small metallic clusters forming discontinuous gold and gallium films, condensed in vacuum onto an insulating substrate (sapphire), was experimentally studied by the method of ultraviolet photoelectron spectroscopy (UPS) for a photon energy of 5.4 eV. It seems that the charging is due to electron emission as well as to electron transfer from metal islands to the empty electron states in the metal-insulator interface.

Condensed Matter::Quantum GasesAnalytical chemistryPhysics::Opticschemistry.chemical_elementSubstrate (electronics)Condensed Matter PhysicsSurfaces Coatings and FilmsElectron transferTransition metalX-ray photoelectron spectroscopychemistrySapphireCondensed Matter::Strongly Correlated ElectronsThin filmGalliumInstrumentationUltraviolet photoelectron spectroscopyVacuum
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