Search results for "spectrum"

showing 10 items of 2043 documents

Subphthalocyanines as narrow band red-light emitting materials

2007

A series of new light emitting subphthalocyanines, lower homologues of phthalocyanines, were synthesized having color points covering the red-orange region of the visible spectrum. Additionally, they were found to be of potential use as narrow band emitters for red-light emitting diodes.

Chemistrybusiness.industryOrganic ChemistryPhotochemistryBiochemistryFluorescencelaw.inventionNarrow bandlawDrug DiscoveryOptoelectronicsRed lightbusinessDiodeVisible spectrumLight-emitting diodeTetrahedron Letters
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Improving the photocatalytic H2 evolution activity of Keggin polyoxometalates anchoring copper-azole complexes

2021

Eliminating the use of precious metals as cocatalysts and using visible light are two important aspects in the field of photocatalytic H2 evolution with polyoxometalates (POMs) as photosensitizers. Here we present two new POM-based materials: [CuII5(2-ptz)6(H2O)4(GeW12O40)]·4H2O (1) and [CuI2(ppz)4][H2GeW12O40]·8H2O (2) (2-ptz = 5-(2-pyridyl) tetrazole, ppz = 3-(pyrid-4-yl) pyrazole) synthesized with the Keggin type [GeW12O40]4− (GeW12) polyanion and copper-azole complexes. The optimum photocatalytic H2 evolution rate of compound 1 without a noble metal cocatalyst is 3813 μmol g−1 h−1, which is 7.6 times higher than that of compound 2 and more than 27 times higher than that of bare GeW12 po…

Chemistrychemistry.chemical_elementengineering.materialPyrazolePhotochemistryPollutionCopperchemistry.chemical_compoundPhotocatalysisengineeringEnvironmental ChemistryNoble metalTetrazolePhotosensitizerDispersion (chemistry)Visible spectrumGreen Chemistry
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Sensitivity of the Cherenkov Telescope Array to spectral signatures of hadronic PeVatrons with application to Galactic Supernova Remnants

2023

The local Cosmic Ray (CR) energy spectrum exhibits a spectral softening at energies around 3~PeV. Sources which are capable of accelerating hadrons to such energies are called hadronic PeVatrons. However, hadronic PeVatrons have not yet been firmly identified within the Galaxy. Several source classes, including Galactic Supernova Remnants (SNRs), have been proposed as PeVatron candidates. The potential to search for hadronic PeVatrons with the Cherenkov Telescope Array (CTA) is assessed. The focus is on the usage of very high energy $\gamma$-ray spectral signatures for the identification of PeVatrons. Assuming that SNRs can accelerate CRs up to knee energies, the number of Galactic SNRs whi…

Cherenkov Telescope ArrayGamma rays: generalstatistical [methods]energy spectrumFOS: Physical sciencesVHESettore FIS/05 - Astronomia E Astrofisicacosmic raysMethods: data analysissupernovadata analysis [methods][PHYS.PHYS.PHYS-INS-DET]Physics [physics]/Physics [physics]/Instrumentation and Detectors [physics.ins-det]Cosmic raysInstrumentation and Methods for Astrophysics (astro-ph.IM)Cherenkov Telescope Arra ; alactic Supernova Remnants ; PeVatrons ;Methods: statisticalgalactic PeVatronsHigh Energy Astrophysical Phenomena (astro-ph.HE)emission spectrum) supernovae: general [(stars]Astronomy and AstrophysicssensitivityobservatoryGalactic PeVatronscosmic radiationspectralgalaxyhadron(Stars:) supernovae: generalAstrophysics - High Energy Astrophysical PhenomenaAstrophysics - Instrumentation and Methods for Astrophysics[PHYS.ASTR]Physics [physics]/Astrophysics [astro-ph]statisticalgeneral [gamma rays]signature
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Gas chromatographic-mass spectrometric analysis of chlorinated phenoxyphenols in the technical chlorophenol formulation ky-5′

1984

Abstract The content of polychlorinated phenoxyphenol (PCPP) impurities in the technical chlorophenol formulation Ky-5 (wood preservative) was studied. The phenolic fraction was shown to contain predioxins and isopredioxins, the structures of the components being verified by gas chromatography mass spectrometry of non-derivatized, methylated and acetylated fractions. 2,6-Dichloro-4-(2,4,6-trichlorophenoxy)phenol and 2,6-dichloro-4-(2,3,4,6-tetrachlorophenoxy)phenol were identified by the comparison of their retention times and the mass spectra of their methyl and acetyl derivatives with those of authentic specimens. The amounts of the above components in Ky-5 were ca. 0.8 and 0.2%, respecti…

ChlorophenolPreservativeChromatographyOrganic ChemistryFraction (chemistry)General MedicineMass spectrometryBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryMass spectrumPhenolGas chromatographyGas chromatography–mass spectrometryJournal of Chromatography A
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FluorMODleaf: A new leaf fluorescence emission model based on the PROSPECT model

2010

International audience; A new model of chlorophyll a fluorescence emission by plant leaves, FluorMODleaf, is presented. It is an extension of PROSPECT, a widely used leaf optical properties model that regards the leaf as a pile of N absorbing and diffusing elementary plates. In FluorMODleaf, fluorescence emission of an infinitesimal layer of thickness dx is integrated over the entire elementary plate. The fluorescence source function is based on the excitation spectrum of diluted isolated thylakoids and on the emission spectra of isolated photosystems, PSI and PSII, which are the main pigment–protein complexes involved in the initial stages of photosynthesis. Scattering within the leaf is p…

Chlorophyll aMaterials scienceTeledetecció010504 meteorology & atmospheric sciencesAnalytical chemistrySoil Science01 natural sciences010309 opticschemistry.chemical_compoundOptics0103 physical sciences[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyEmission spectrumComputers in Earth SciencesChlorophyll fluorescence0105 earth and related environmental sciencesRemote sensing[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Scatteringbusiness.industryAbsorption cross sectionGeologyFluorescenceFluorescènciachemistryChlorophyllQuantum efficiencybusiness
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Refinement of a structural model of a pigment-protein complex by accurate optical line shape theory and experiments.

2007

Time-local and time-nonlocal theories are used in combination with optical spectroscopy to characterize the water-soluble chlorophyll binding protein complex (WSCP) from cauliflower. The recombinant cauliflower WSCP complexes reconstituted with either chlorophyll b (Chl b) or Chl a/Chl b mixtures are characterized by absorption spectroscopy at 77 and 298 K and circular dichroism at 298 K. On the basis of the analysis of these spectra and spectra reported for recombinant WSCP reconstituted with Chl a only (Hughes, J. L.; Razeghifard, R.; Logue, M.; Oakley, A.; Wydrzynski, T.; Krausz, E. J. Am. Chem. Soc. U.S.A. 2006, 128, 3649), the "open-sandwich" model proposed for the structure of the pig…

Chlorophyll bChlorophyllModels MolecularCircular dichroismOptics and PhotonicsAbsorption spectroscopyChemistryDimerExcitonChlorophyll ACircular DichroismSpectrum AnalysisStatic ElectricityLight-Harvesting Protein ComplexesBrassicaSpectral lineSurfaces Coatings and Filmschemistry.chemical_compoundCrystallographyKineticsModels ChemicalMaterials ChemistryChlorophyll bindingPhysical and Theoretical ChemistrySpectroscopyThe journal of physical chemistry. B
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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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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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Analysis of pyridoquinoline derivatives by liquid chromatography/atmospheric pressure chemical ionization mass spectrometry

2001

A method using liquid chromatography/atmospheric pressure chemical ionization mass spectrometry (LC/APCI-MS) has been developed for the characterization and determination of pyridoquinoline derivatives 4,6-bis(dimethylaminoethylamino)-2,8,10-trimethylpyrido[3,2-g]quinoline, 4,6-bis(dimethylaminoethoxy)-2,8,10-trimethylpyrido[3,2-g]quinoline and 4,6-bis[(dimethylaminoethyl)thio]-2,8,10-trimethylpyrido[3,2-g] quinoline, all with potential antitumor properties. LC separation was performed on a conventional C18 column using a binary mobile phase composed of acetonitrile and 50 mM aqueous ammonium formate at pH 3. The APCI mass spectra obtained showed that proton addition giving [M + H]+ was the…

ChromatographyAqueous solutionOrganic ChemistryQuinolineAnalytical chemistryAtmospheric-pressure chemical ionizationMass spectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryIonizationAmmonium formateMass spectrumAcetonitrileSpectroscopyRapid Communications in Mass Spectrometry
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Comparison of liquid chromatography using triple quadrupole and quadrupole ion trap mass analyzers to determine pesticide residues in oranges.

2005

Liquid chromatography-triple quadrupole/mass spectrometry (LC-TQ/MS) and liquid chromatography-quadrupole ion trap/mass spectrometry (LC-QIT/MS) for determining bupirimate, hexaflumuron, tebufenpyrad, buprofezin, pyriproxyfen, and fluvalinate in fruits have been compared. The differences in the mass spectra obtained by triple and ion trap quadrupoles are discussed, showing how both of them provide interesting features. The evaluation of the two instruments was carried out by ethyl acetate extraction of oranges spiked with the studied pesticides at LOQ and 10 times the LOQ. Results obtained by LC-TQ/MS correlated well with those obtained by LC-QIT/MS. Recoveries were 70-94% by LC-TQ/MS and 7…

ChromatographyChemistryOrganic ChemistryAnalytical chemistryPesticide ResiduesGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical ChemistryTriple quadrupole mass spectrometerStandard additionMass spectrumSample preparationIon trapQuadrupole ion trapChromatography LiquidCitrus sinensisJournal of chromatography. A
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