Search results for "Acceptor"

showing 10 items of 394 documents

Ultrafast Twisting of the Indoline Donor Unit Utilized in Solar Cell Dyes: Experimental and Theoretical Studies

2015

Previous time-resolved measurements on D149, the most-studied dye of the indoline family, had shown a fast time-component of 20–40 ps that had tentatively been attributed to structural relaxation. Using femtosecond transient absorption, we have investigated the isolated indoline donor unit (i.e., without acceptor group) and found an ultrafast decay characterized by two lifetimes of 3.5 and 23 ps. Density functional theory calculations show π-bonding and π*-antibonding character of the central ethylene group for the highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO), respectively. The LUMO is localized on the flexible vinyl-diphenyl region of the donor unit and a twist…

ChemistryRelaxation (NMR)PhotochemistryAcceptorSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyExcited stateUltrafast laser spectroscopyIndolineDensity functional theoryMolecular orbitalPhysical and Theoretical ChemistryHOMO/LUMOThe Journal of Physical Chemistry C
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Orbital-Resolved Partial Charge Transfer from the Methoxy Groups of Substituted Pyrenes in Complexes with Tetracyanoquinodimethane—A NEXAFS Study

2012

It is demonstrated that the near-edge X-ray absorption fine structure (NEXAFS) provides a powerful local probe of functional groups in novel charge transfer (CT) compounds and their electronic properties. Microcrystals of tetra-/hexamethoxypyrene as donors with the strong acceptor tetracyano-p-quinodimethane (TMP/HMP-TCNQ) were grown by vapor diffusion. The oxygen and nitrogen K-edge spectra are spectroscopic fingerprints of the functional groups in the donor and acceptor moieties, respectively. The orbital selectivity of the NEXAFS pre-edge resonances allows us to precisely elucidate the participation of specific orbitals in the charge transfer process. Upon complex formation, the intensit…

ChemistryResonanceGeneral ChemistryPhotochemistryBiochemistryAcceptorTetracyanoquinodimethaneCatalysisXANESSpectral linechemistry.chemical_compoundPartial chargeColloid and Surface ChemistryAtomic orbitalSelectivityJournal of the American Chemical Society
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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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Oligo(phenylenvinylene) mit terminaler Donor-Acceptor-Substitution

2002

ChemistryStereochemistrySubstitution (logic)General MedicineDonor acceptorAngewandte Chemie
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ChemInform Abstract: Thermal 1,6-Electrocyclization Reactions of Acceptor-Substituted 2,3-Divinyl-1H-indoles Yielding Functionalized Carbazoles.

1990

Three new synthetic procedures for and thermal 1,6-electrocyclizations of acceptor-substituted 2,3-divinyl-1H-indoles leading to functionalizing carbazoles are described. The scope and limitations as well as some mechanistic aspects of the methodologies are discussed. The key strategies employed include Pd(II)-catalyzed coupling and Wittig procedures.

ChemistryWittig reactionGeneral MedicineCombinatorial chemistryAcceptorChemInform
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Wittig-Olefinierung zu neuen donor- und akzeptor-substituierten 3-Vinylindolen: Optimierte Syntheseverfahren

1989

The optimized Wittig reaction of selectively functionalized 3-acylindoles yield new, and for Diels-Alder reactions highly reactive donor- and acceptor substituted 3-vinylindoles, respectively.

ChemistryYield (chemistry)fungiWittig reactionOrganic chemistryGeneral ChemistryAcceptorMonatshefte für Chemie - Chemical Monthly
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Assessing and modeling nitrite inhibition in microalgae-bacteria consortia for wastewater treatment by means of photo-respirometric and chlorophyll f…

2022

Abstract Total nitrite (TNO2 = HNO2 + NO−2) accumulation due to the activity of ammonia-oxidizing bacteria (AOB) was monitored in microalgae-bacteria consortia, and the inhibitory effect of nitrite/free nitrous acid (NO2-N/FNA) on microalgae photosynthesis and inhibition mechanism was studied. A culture of Scenedesmus was used to run two sets of batch reactors at different pH and TNO2 concentrations to evaluate the toxic potential of NO2-N and FNA. Photo-respirometric tests showed that NO2-N accumulation has a negative impact on net oxygen production rate (OPRNET). Chlorophyll a fluorescence analysis was used to examine the biochemical effects of NO2-N stress and the mechanism of NO2-N inhi…

ChlorophyllPhotosynthetic reaction centrechemistry.chemical_classificationNitrous acidChlorophyll aEnvironmental EngineeringBacteriabiologyChemistryChlorophyll AElectron acceptorbiology.organism_classificationPollutionFluorescenceWater Purificationchemistry.chemical_compoundMicroalgaeEnvironmental ChemistryNitriteWaste Management and DisposalChlorophyll fluorescenceNitritesScenedesmusPhotosystemNuclear chemistryScience of The Total Environment
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Supported liquid membrane extraction of glyphosate metabolites

2001

Use of the supported liquid membrane (SLM) technique for (aminomethyl)phosphonic acid (AMPA) extraction is presented. For the extraction of this analyte a suitable SLM system involves a liquid membrane containing Aliquat 336 – a cationic carrier that facilitates AMPA transport. The extraction of this compound, as in the case of glyphosate, is dependent on the donor phase pH and the concentration and type of counter-ion in the acceptor phase, although some differences are also observed. In both cases the transport mechanism is counter-coupled transport in which the driving force of mass transport over the membrane is created by the gradient of chloride anions from the acceptor to donor phase.

ChromatographyChemistryExtraction (chemistry)Filtration and SeparationAliquat 336ChlorideAcceptorAnalytical Chemistrychemistry.chemical_compoundMembraneLiquid–liquid extractionMass transferPhase (matter)medicinemedicine.drugJournal of Separation Science
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Supported liquid membrane extraction of aromatic aminophosphonates

2001

Abstract A fast and efficient supported liquid membrane (SLM) extraction system for the series of substituted aromatic aminophosphonates was elaborated. The mass transfer of solute was examined in terms of operator (pH and ionic strength of water phase, composition of membrane phase and the concentration of analyte) dependent parameters. Additionally, the influence of the aminophosphonates structure on the extraction efficiency was examined. From the results it can be concluded that the most effective conditions of membrane process are 10% (w/w) carrier concentration (Aliquat 336) in the liquid membrane, high pH of donor phase (pH=11) and moderate salt concentration (0.4 M NaCl) in the acce…

ChromatographyaminophosphonatesChemistryExtraction (chemistry)Inorganic chemistryAliquat 336BiochemistryAcceptorAnalytical ChemistryMembrane technologychemistry.chemical_compoundMembraneIonic strengthPhase (matter)Mass transferextractionEnvironmental Chemistrysupported liquid membraneSpectroscopyAnalytica Chimica Acta
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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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