Search results for "PHOTOCHEMISTRY"

showing 10 items of 2034 documents

Characterisation of Chlorophyll a and Chlorophyll b Monomers in Various Solvent Environments with Ultrafast Spectroscopy

1998

In photosynthesis the energy from the sun is captured by light harvesting chlorophyll pigments and converted to stable chemical energy, by the photochemical reaction center. Photosynthetic energy transfer in the antenna systems of green plants has previously been studied by ultrafast time resolved spectroscopy. The characteristics of the chlorophyll pigments itself is important to study in order to understand the dynamics on a femtosecond timescale. One way to study the energy transfer is to use transient absorption spectroscopy and follow the increase or decrease in the transient absorption signal with time (1). Another way to study the energy transfer is to monitor the change in dichroism…

Chlorophyll bPhysics::Biological Physics0303 health sciencesChlorophyll aMaterials scienceDichroism010402 general chemistryPhotochemistry7. Clean energy01 natural sciences0104 chemical sciencesLight-harvesting complex03 medical and health scienceschemistry.chemical_compoundchemistryChlorophyllUltrafast laser spectroscopyTime-resolved spectroscopySpectroscopy030304 developmental biology
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Effects of chlorophyll a, chlorophyll b, and xanthophylls on the in vitro assembly kinetics of the major light-harvesting chlorophyll a/b complex, LH…

2001

The major light-harvesting chlorophyll a/b complex (LHCIIb) of photosystem II in higher plants can be reconstituted with pigments in lipid-detergent micelles. The pigment-protein complexes formed are functional in that they perform efficient internal energy transfer from chlorophyll b to chlorophyll a. LHCIIb formation in vitro, can be monitored by the appearance of energy transfer from chlorophyll b to chlorophyll a in time-resolved fluorescence measurements. LHCIIb is found to form in two apparent kinetic steps with time constants of about 30 and 200 seconds. Here we report on the dependence of the LHCIIb formation kinetics on the composition of the pigment mixture used in the reconstitut…

Chlorophyll bchemistry.chemical_classificationChlorophyll afood and beveragesLight-harvesting complexes of green plantsPhotochemistrychemistry.chemical_compoundB vitaminschemistryNeoxanthinStructural BiologyChlorophyllXanthophyllChlorophyll bindingMolecular BiologyJournal of Molecular Biology
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Filling the “green gap” of the major light-harvesting chlorophyll a/b complex by covalent attachment of Rhodamine Red

2009

AbstractThe major light-harvesting chlorophyll a/b complex (LHCII) greatly enhances the efficiency of photosynthesis in green plants. Recombinant LHCII can be assembled in vitro from its denatured, bacterially expressed apoprotein and plant pigments. This makes it an interesting candidate for biomimetic light-harvesting in photovoltaic applications. Due to its almost 20 pigments bound per apoprotein, LHCII absorbs efficiently in the blue and red spectral domains of visible light but less efficiently in the green domain, the so-called “green gap” in its absorption spectrum. Here we present a hybrid complex of recombinant LHCII with organic dyes that add to LHCII absorption in the green spect…

ChlorophyllLHCIIProtein FoldingFRET (Förster resonance energy transfer)Chlorophyll aAbsorption spectroscopyBiophysicsPhotosynthesisPhotochemistryBiochemistryRhodamineLight-harvesting complexchemistry.chemical_compoundPhotosynthesisFluorescent DyesRhodaminesChlorophyll Afood and beveragesSite-specific labelingCell BiologyMaleimide dyeB vitaminsSolar spectrumchemistryChlorophyllVisible spectrumBiochimica et Biophysica Acta (BBA) - Bioenergetics
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Hierarchical Self-Organization of Perylene Bisimide–Melamine Assemblies to Fluorescent Mesoscopic Superstructures

2000

A series of three perylene tetracarboxylic acid bisimide dyes 3a-c bearing phenoxy substituents at the four bay positions of the perylene core were synthesized and their complexation behavior to complementary ditopic dialkyl melamines 8a-c was investigated. Binding constants and Gibbs binding energies for the hydrogen bonds between the imide and the complementary melamine moiety have been determined in several solvents by NMR and UV/Vis titration experiments with monotopic model compounds 5 and 9. The effects of the solvent polarity and specific solvent-solute interactions on the degree of polymerization of (3 x 8)n are discussed, and a general formula to estimate the chain length of [AA-BB…

ChlorophyllMagnetic Resonance SpectroscopyLightPolymersMolecular ConformationSupramolecular chemistryDegree of polymerizationImidesPhotochemistryFluorescenceCatalysischemistry.chemical_compoundNon-covalent interactionsPerylenechemistry.chemical_classificationMicroscopy ConfocalTriazinesHydrogen bondOrganic ChemistryOptical polarizationPolymerGeneral ChemistrySolutionsSupramolecular polymersMicroscopy ElectronchemistrySpectrophotometry UltravioletPeryleneChemistry – A European Journal
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Optically Detected Magnetic Resonance of Chlorophyll Triplet States in Water-Soluble Chlorophyll Proteins from Lepidium virginicum: Evidence for Exci…

2018

Optically detected magnetic resonance of triplet states populated by photoexcitation in water-soluble chlorophyll proteins (WSCPs) from Lepidium virginicum has been performed using both absorption and fluorescence detection. Well resolved triplet-singlet (T-S) spectra have been obtained and interpreted in terms of electronic interactions among the four chlorophylls (Chls), forming two dimers in the WSCP tetramer. Localization of the triplet state on a single Chl leads to a redistribution of the oscillator strength in the remaining three Chls of the complex. By comparing the spectra with those obtained on a substoichiometric WSCP complex containing only 2 Chls per protein tetramer, we proved…

ChlorophyllMaterials Chemistry2506 Metals and Alloys0301 basic medicineOscillator strength010402 general chemistryPhotochemistryLepidium01 natural sciencesCoatings and Films03 medical and health scienceschemistry.chemical_compoundTetramerMaterials ChemistryPhysical and Theoretical Chemistry; Surfaces Coatings and Films; Materials Chemistry2506 Metals and AlloysPhysical and Theoretical ChemistryTriplet stateNuclear Magnetic Resonance BiomolecularPlant ProteinsChemistryTemperatureWaterChromophorePorphyrinFluorescenceRecombinant Proteins0104 chemical sciencesSurfaces Coatings and FilmsSurfacesPhotoexcitation030104 developmental biologySolubilityChlorophyllThe Journal of Physical Chemistry B
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Evidence for two spectroscopically different dimers of light-harvesting complex I from green plants

2000

A preparation consisting of isolated dimeric peripheral antenna complexes from green plant photosystem I (light-harvesting complex I or LHCI) has been characterized by means of (polarized) steady-state absorption and fluorescence spectroscopy at low temperatures. We show that this preparation can be described reasonably well by a mixture of two types of dimers. In the first dimer about 10% of all Q(y)() absorption of the chlorophylls arises from two chlorophylls with absorption and emission maxima at about 711 and 733 nm, respectively, whereas in the second about 10% of the absorption arises from two chlorophylls with absorption and emission maxima at about 693 and 702 nm, respectively. The…

ChlorophyllP700Photosystem IIPhotosystem I Protein ComplexChemistryDimerCircular DichroismPhotosynthetic Reaction Center Complex ProteinsLight-Harvesting Protein ComplexesPhotosystem II Protein ComplexPhotochemistryPhotosystem IBiochemistryZea maysFluorescence spectroscopychemistry.chemical_compoundSpectrometry FluorescenceLight harvesting complex ISpectrophotometryAbsorption (chemistry)Protein Structure QuaternaryDimerization
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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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Characterization of the Fast and Slow Reversible Components of Non-Photochemical Quenching in Isolated Pea Thylakoids by Picosecond Time-Resolved Chl…

1999

The fast and slow reversible components of non-photochemical chlorophyll fluorescence quenching commonly assigned to the qE and the qI mechanism have been studied in isolated pea thylakoids which were prepared from leaves after a moderate photoinhibitory treatment. Chlorophyll fluorescence decays were measured at picosecond resolution and analyzed on the basis of the heterogeneous exciton/radical pair equilibrium model. Our results show that the fast reversible non-photochemical quenching is completely assigned to the PS II antenna and is related to zeaxanthin. The slow reversible qI type quenching is located at the PS II reaction center and involves enhanced nonradiative decay of the prima…

ChlorophyllPhotosynthetic reaction centrePhotoinhibitionQuenching (fluorescence)ChemistryNon-photochemical quenchingPeasPhotochemistryBiochemistryKineticsSpectrometry FluorescencePicosecondExcited stateThylakoidChlorophyll fluorescencePlant ProteinsBiochemistry
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Water soluble chlorophyll binding protein of higher plants: A most suitable model system for basic analyses of pigment–pigment and pigment–protein in…

2011

Abstract This short review paper describes spectroscopic studies on pigment–pigment and pigment–protein interactions of chlorophyll (Chl) a and b bound to the recombinant protein of class IIa water soluble chlorophyll protein (WSCP) from cauliflower. Two Chls form a strongly excitonically coupled open sandwich dimer within the tetrameric protein matrix. In marked contrast to the mode of excitonic coupling of Chl and bacterio-Chl molecules in light harvesting complexes and reaction centers of all photosynthetic organisms, the unique structural pigment array in the Chl dimer of WSCP gives rise to an upper excitonic state with a large oscillator strength. This property opens the way for thorou…

ChlorophyllPhysiologyTetrameric proteinDimerLight-Harvesting Protein ComplexesTemperatureWatermacromolecular substancesPlant SciencePlantsPhotochemistryPhotosynthesisModels BiologicalLight-harvesting complexchemistry.chemical_compoundPigmentchemistryChlorophyllvisual_artvisual_art.visual_art_mediumChlorophyll bindingMoleculeAgronomy and Crop ScienceJournal of Plant Physiology
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Visible-light driven oxidation of gaseous aliphatic alcohols to the corresponding carbonyls via TiO2 sensitized by a perylene derivative

2013

Sensitized P25 TiO2 was prepared by wet impregnation with a home-prepared perylene dye, i.e., N,N?-bis(2-(1- piperazino)ethyl)-3,4,9,10-perylene-tetracarboxylic acid diimide dichloride (PZPER). Energy levels of PZPER were found to be compatible with those of TiO2 allowing fast electron transfer. The obtained catalyst has been characterized and used in the gas-phase partial oxidation of aliphatic primary and secondary alcohols, i.e., methanol, ethanol, and 2- propanol. The reaction was carried out under cut-off (?> 400 nm) simulated solar radiation in O2 atmosphere. The perylene derivative allowed a good absorbance of visible radiation thanks to its low optical energy gap (2.6 eV) which was …

Chromatography GasLightHealth Toxicology and MutagenesisInorganic chemistryFormaldehydeElectronsPhotochemistry..ImidesCatalysisCatalysischemistry.chemical_compoundDiimideEnvironmental ChemistryReactivity (chemistry)Partial oxidationVisible light photocatalysisPeryleneTitaniumSettore ING-IND/24 - Principi Di Ingegneria ChimicaMolecular StructureMethanolPerylene-sensitized TiO2General MedicinePollutionAliphatic alcohol oxidationchemistryYield (chemistry)MethanolPerylene-sensitized TiO2 Visible light photocatalysis Aliphatic alcohol oxidationOxidation-ReductionPerylene
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