Search results for "Acceptor"

showing 10 items of 394 documents

Rho-mediated activation of PI(4)P5K and lipid second messengers is necessary for promotion of angiogenesis by Semaphorin 4D

2011

Phosphatidylinositol 4-phosphate 5-kinase (PI(4)P5K) is a type I lipid kinase that generates the lipid second messenger phospholipid phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) and functions downstream of RhoA in actin organization. It is known to play an essential role in neurite remodeling, yielding a phenotype identical to that seen in cells treated with Semaphorin 4D (Sema4D), a protein that regulates proliferation, adhesion and migration in many different cell types. Plexin-B1, the receptor for Sema4D, activates RhoA in order to generate a pro-angiogenic signal in endothelial cells. Therefore, we looked in human umbilical vein endothelial cells (HUVEC) to determine if Plexin-B1 e…

Phosphatidylinositol 45-DiphosphateCancer ResearchRHOAPhysiologyAngiogenesisSemaphorin 4DClinical BiochemistrySEMA4DNeovascularization PhysiologicNerve Tissue ProteinsReceptors Cell SurfaceSemaphorinsSynaptojaninBiologySecond Messenger SystemsArticlePI(45)P2chemistry.chemical_compoundAntigens CDRhoSettore BIO/10 - BiochimicaHumansPlexin B1PhosphatidylinositolRho-associated protein kinaseCytoskeletonrho-Associated KinasesPI(4)P5KKinaseCell biologyPhosphotransferases (Alcohol Group Acceptor)AngiogenesiHEK293 CellschemistrySecond messenger systembiology.proteinCalciumrhoA GTP-Binding ProteinAngiogenesis
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Control of cellular phosphatidylinositol 4,5-bisphosphate levels by adhesion signals and Rho GTPases in NIH 3T3 fibroblasts

2000

The involvement of small GTPases of the Rho family in the control of phosphoinositide metabolism by adhesion signals was examined in NIH 3T3 fibroblasts. Abrogation of adhesion signals by detachment of cells from their substratum resulted in a time-dependent decrease in the cellular level of PtdIns(4,5)P2 by approximately 50%. This effect could be mimicked by treatment of adherent cells with Clostridium difficile toxin B and toxin B-1470, which inhibit specific subsets of Rho and Ras GTPases. Detachment of cells that had been pretreated with the clostridial toxins did not cause a further reduction in PtdIns(4,5)P2 levels, suggesting that the target GTPases are integrated into the control of…

Phosphatidylinositol 45-Diphosphaterac1 GTP-Binding Proteinrho GTP-Binding ProteinsBacterial ToxinsCellClostridium difficile toxin BRAC1GTPasePhospholipaseBiologyTransfectionBiochemistryMicechemistry.chemical_compoundPhosphoinositide Phospholipase CBacterial ProteinsCell AdhesionmedicineAnimalsPhosphorylationInositol phosphatechemistry.chemical_classificationPhospholipase CCytotoxinsPhosphoric Diester Hydrolases3T3 CellsMolecular biologyRecombinant ProteinsCell biologyKineticsPhosphotransferases (Alcohol Group Acceptor)medicine.anatomical_structurechemistryPhosphatidylinositol 45-bisphosphateType C PhospholipasesCalciumSignal TransductionEuropean Journal of Biochemistry
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Bis-Sulfone- and Bis-Sulfoxide-Spirobifluorenes: Polar Acceptor Hosts with Tunable Solubilities for Blue-Phosphorescent Light-Emitting Devices

2016

Bis-sulfone- and bis-sulfoxide-spirobifluorenes are a promising class of high-triplet-energy electron-acceptor hosts for blue phosphorescent light-emitting devices. The molecular design and synthetic route are simple and facilitate tailoring of the solubilities of the host materials without lowering the high-energy triplet state. The syntheses and characterization (including single-crystal structures) of four electron-accepting hosts are reported; the trend in their reduction potentials is consistent with the electron-withdrawing nature of the sulfone or sulfoxide substituents. Emission maxima of 421–432 nm overlap with the MLCT absorption of the sky-blue emitter bis(4,6-difluorophenyl-pyri…

Phosphine oxidechemistry.chemical_classificationOrganic ChemistrySulfoxide02 engineering and technologyElectron acceptor010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesAcceptor0104 chemical sciencesSulfonechemistry.chemical_compoundchemistryOLEDPhysical and Theoretical ChemistryTriplet state0210 nano-technologyPhosphorescenceEuropean Journal of Organic Chemistry
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Impact of the position isomer of the linkage in the double D–A branch-based organic dyes on the photovoltaic performance

2014

Abstract Three organic dyes with double D–A system were synthesized and applied in the dye-sensitized solar cells. These dyes contain phenothiazine as an electron donor and cyanoacetic acid as an acceptor/anchor. Linkages were incorporated at the ortho-, meta- and para-positions and their impact on the performance of photovoltaic was observed. Among them, the dye with a para-position linkage exhibited the highest short-circuit photocurrent density (12.26 mA cm−2) and open-circuit photovoltage (756 mV), leading to the best overall efficiency (6.14%) due to better light harvesting capacity under standard global 1.5 AM conditions. Under similar measuring conditions the dyes with ortho and meta…

PhotocurrentProcess Chemistry and TechnologyGeneral Chemical EngineeringPhotovoltaic systemElectron donorLinkage (mechanical)PhotochemistryAcceptorlaw.inventionDye-sensitized solar cellchemistry.chemical_compoundCyanoacetic acidchemistrylawPhenothiazineDyes and Pigments
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PV and magnetic field effects in poly(3-hexylthiophene)-fullerene cells doped with phthalocyanine soluble derivative

2007

An attempt was made to widen the photosensitivity spectral range of poly(3-hexylthiophene)-fullerene blend by adding an extra electron donor — a newly synthesized soluble phthalocyanine derivative (SnClPc) having the electron absorption band at 708 nm. As the electron acceptor, home-synthesised di(ethoxycarbonyl) methano-fullerene carboxylate (C 61 (CO 2 Et) 2 ) was used, and as the hole transporter — the regioregular poly 3-hexylthiophene (P3HT). The sandwich-type samples were prepared on an ITO glass substrate by coating it with a 30–50 nm thick PEDOT:PSS layer followed by a ~100 nm thick P3HT:C 61 (CO 2 Et) 2 :SnClPc blend. For the top electrodes In or Au were used. Spectral dependences …

Photocurrentchemistry.chemical_classificationChemistryDopingAnalytical chemistryElectron acceptorCondensed Matter PhysicsElectronic Optical and Magnetic Materialschemistry.chemical_compoundPhotosensitivityPEDOT:PSSAbsorption bandPhthalocyanineOrganic chemistryQuantum efficiencyInstrumentationThe European Physical Journal Applied Physics
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Synthesis and photovoltaic performance of asymmetric di-anchoring organic dyes

2015

Abstract Two novel metal-free organic dyes bearing two asymmetric double donor–acceptor segments were synthesized. Their physical, optical, electrochemical properties and photovoltaic performances were investigated. Compared with the mono-anchoring dye containing single donor–acceptor chain, these new dyes exhibited a broader and much stronger absorption in the light wavelength ranging from 400 to 600 nm, showed higher IPCE values and short-circuit current density, which led to more efficient photovoltaic performance. The dye with triphenylamine and phenothiazine as two electron donors and two cyanoacrylic acids as two electron acceptors exhibited an impressive power conversion efficiency o…

Photocurrentchemistry.chemical_classificationMaterials scienceProcess Chemistry and TechnologyGeneral Chemical EngineeringEnergy conversion efficiencyElectron acceptorPhotochemistryElectrochemistryTriphenylaminechemistry.chemical_compoundDye-sensitized solar cellchemistryPhenothiazineAbsorption (electromagnetic radiation)Dyes and Pigments
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Intramolecular charge transfer in elongated donor-acceptor conjugated polyenes

1995

Abstract Intramolecular charge transfer (ICT) has been investigated by electro-optical absorption measurements for two series of donor-acceptor polyenes of increasing length. Each molecule undergoes an increase in dipole moment upon photoexcitation. The experimental results indicate that lengthening the polyenic chain linking the donor and acceptor end groups results in a bathochromic shift of the ICT absorption band and induces marked increases of both excited state and transition dipoles, whereas the ground-state dipole is relatively unaffected. As a result, marked photoinduced changes in the dipole moment (up to 33 D) were obtained with the longest molecules (up to 27 A) leading to highl…

PhotoexcitationBond dipole momentDipoleChemistryAbsorption bandIntramolecular forceExcited stateBathochromic shiftGeneral Physics and AstronomyPhysical and Theoretical ChemistryPhotochemistryAcceptorChemical Physics Letters
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Single-molecule spectroscopy of molecular aggregates at low temperature

2004

We have conducted single-molecule spectroscopy of a fluorescent polyphenylene dendrimer consisting of four peripheral perylenemonoimides which serve as energy donors and a central terrylenediimide which is the energy acceptor. After selective excitation of the donors the low-temperature emission spectra of single dendrimers show the purely electronic zero-phonon line as the most prominent feature of the acceptor. These sharp emission lines are subjected to appreciable spectral shifts. Fluorescence excitation spectroscopy of individual dendrimers in the spectral region of the donor absorption allows to extract energy transfer rates for single donors within the dendrimer. Although the energy …

PhotoluminescenceChemistryExcitonBiophysicsAnalytical chemistryGeneral ChemistryCondensed Matter PhysicsPhotochemistryBiochemistryAcceptorFluorescenceAtomic and Molecular Physics and OpticsDendrimerEmission spectrumSpectroscopyAbsorption (electromagnetic radiation)Journal of Luminescence
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Energy of excitons and acceptor–exciton complexes to explain the origin of ultraviolet photoluminescence in ZnO quantum dots embedded in a SiO2 matrix

2011

Abstract Assuming finite depth and within the effective mass approximation, the energies of exciton states and of the acceptor–exciton complexes confined in spherical ZnO quantum dots (QDs) embedded in a SiO2 matrix are calculated using a matrix procedure, including a three-dimensional confinement of carrier in the QDs. This theoretical model has been designed to illustrate the two emission bands in the UV region observed in our experimental Photoluminescence spectrum (PL), with the first emission band observed at 3.04 eV and attributed to the bound ionized acceptor–exciton complexes, and the second one located at 3.5 and assigned to the free exciton. Our calculations have revealed a good a…

PhotoluminescenceCondensed Matter::OtherChemistryExcitonGeneral ChemistryCondensed Matter::Mesoscopic Systems and Quantum Hall EffectCondensed Matter Physicsmedicine.disease_causeAcceptorCondensed Matter::Materials ScienceMatrix (mathematics)Quantum dotIonizationMaterials ChemistrymedicineAtomic physicsUltravioletBiexcitonSolid State Communications
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Recombination processes in unintentionally doped GaTe single crystals

2002

Emission spectra of GaTe single crystals in the range of 1.90–1.38 eV have been analyzed at different temperatures and excitation intensities by photoluminescence, photoluminescence excitation, and selective photoluminescence. A decrease in band gap energy with an increase in temperature was obtained from the redshift of the free exciton recombination peak. The energy of longitudinal optical phonons was found to be 14±1 meV. A value of 1.796±0.001 eV for the band gap at 10 K was determined, and the bound exciton energy was found to be 18±0.3 meV. The activation energy of the thermal quenching of the main recombination peaks and of the ones relating to the ionization energy of impurities and…

PhotoluminescenceImpurity statesBand gapChemistryExcitonGallium compounds ; III-VI semiconductors ; Photoluminescence ; Impurity states ; Cefect states ; Electron-phonon interactions ; Phonon-exciton interactions ; Excitons ; Red shift ; Radiation quenchingDopingGallium compoundsRadiation quenchingUNESCO::FÍSICAIII-VI semiconductorsGeneral Physics and AstronomyPhonon-exciton interactionsCefect statesAcceptorRed shiftElectron-phonon interactionsCondensed Matter::Materials Science:FÍSICA [UNESCO]ExcitonsPhotoluminescence excitationEmission spectrumIonization energyAtomic physicsPhotoluminescence
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