Search results for "Electron donor"

showing 10 items of 64 documents

Lack of a peroxiredoxin suppresses the lethality of cells devoid of electron donors by channelling electrons to oxidized ribonucleotide reductase

2017

The thioredoxin and glutaredoxin pathways are responsible of recycling several enzymes which undergo intramolecular disulfide bond formation as part of their catalytic cycles such as the peroxide scavengers peroxiredoxins or the enzyme ribonucleotide reductase (RNR). RNR, the rate-limiting enzyme of deoxyribonucleotide synthesis, is an essential enzyme relying on these electron flow cascades for recycling. RNR is tightly regulated in a cell cycle-dependent manner at different levels, but little is known about the participation of electron donors in such regulation. Here, we show that cytosolic thioredoxins Trx1 and Trx3 are the primary electron donors for RNR in fission yeast. Unexpectedly,…

0301 basic medicineCancer ResearchThioredoxin reductaseSynthesis PhaseYeast and Fungal ModelsBiochemistryElectron DonorsSchizosaccharomyces PombeThioredoxinsGlutaredoxinCell Cycle and Cell DivisionGenetics (clinical)Chemical ReactionsOxidesPeroxidesNucleic acidsChemistryRibonucleotide reductaseBiochemistryExperimental Organism SystemsCell ProcessesSchizosaccharomyces pombePhysical SciencesSynthesis phaseThioredoxinOxidation-ReductionResearch ArticleDNA Replicationlcsh:QH426-470DNA transcriptionElectron donorsBiologyDNA replicationResearch and Analysis MethodsCatalysisElectron Transport03 medical and health sciencesModel OrganismsSchizosaccharomycesRibonucleotide ReductasesOxidationGeneticsMolecular BiologyEcology Evolution Behavior and SystematicsGlutaredoxinsCell growthDNA replicationChemical CompoundsOrganismsFungiBiology and Life SciencesCell BiologyDNAPeroxiredoxinsbiology.organism_classificationYeastCell cycle and cell divisionCheckpoint Kinase 2lcsh:Genetics030104 developmental biologySchizosaccharomyces pombeGene expressionSchizosaccharomyces pombe ProteinsPeroxiredoxin
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Impact of hydroxy and octyloxy substituents of phenothiazine based dyes on the photovoltaic performance

2013

Two novel organic dyes containing hydroxy and octyloxy substituents onto a phenothiazine skeleton were synthesized and their effects on the photovoltaic performance were studied. Hydroxy acts as an ancillary anchoring unit along with the carboxylic group, while the phenothiazine modified moiety acts as an electron donor. The photophysical and electrochemical studies revealed that maximum absorbance of the dye with the hydroxy group in the solution was blue shifted and its band gap increased, indicating that donor acceptor strength was reduced as compared to the octyloxy substituted dye. Furthermore, electron lifetime of the organic dye with the hydroxy moiety was shorter due to smaller resi…

Absorbancechemistry.chemical_compoundDye-sensitized solar cellchemistryBand gapProcess Chemistry and TechnologyGeneral Chemical EngineeringPhenothiazineEnergy conversion efficiencyMoietyElectron donorPhotochemistryElectrochemistryDyes and Pigments
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Amplified spontaneous emission of pyranyliden derivatives in PVK matrix

2016

One of the well-known red light emitting laser dyes is 4-(dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4Hpyran ( DCM ). Amplified spontaneous emission (ASE) has been widely investigated of DCM molecules or its derivatives in polymer or low molecular weight matrix. The main issue for these molecules is aggregation which limits doping concentration in matrix. Lowest ASE threshold values within concentration range of 2 and 4 wt% were obtained. In this work ASE properties of two original DCM derivatives in poly(N-vinylcarbazole) ( PVK ) at various concentrations will be discussed. One of the derivatives is the same DCM dye with replaced butyl groups at electron donor part with bulky try…

Amplified spontaneous emissionDye laserPhotoluminescencebusiness.industryChemistrySolvationQuantum yieldElectron donor02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryThreshold energy01 natural sciences0104 chemical scienceschemistry.chemical_compoundOptoelectronics0210 nano-technologyLuminescencebusinessSPIE Proceedings
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Stimulated emission and optical properties of pyranyliden fragment containing compounds in PVK matrix

2017

This work has been supported by National Research program “Multifunctional materials and composites, photonics and nanotechnology (IMIS2)”. Financial support provided by Scientific Research Project for Students and Young Researchers No. SJZ2015/12 realised at the Institute of Solid State Physics, University of Latvia is greatly acknowledged.

Amplified spontaneous emissionPhotoluminescenceMaterials scienceQuantum yieldElectron donor02 engineering and technologyPhotochemistry01 natural sciences010309 opticschemistry.chemical_compound0103 physical sciences:NATURAL SCIENCES:Physics [Research Subject Categories]Stimulated emissionElectrical and Electronic EngineeringAmplified spontaneous emissionGlass forming low molecular weight compoundsDCMLaser dyeDye laser021001 nanoscience & nanotechnologyThreshold energyAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialschemistryPyranyliden derivatives0210 nano-technologyMethyl group
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Organic solvent desorption from two tegafur polymorphs.

2013

Desorption behavior of 8 different solvents from α and β tegafur (5-fluoro-1-(tetrahydro-2-furyl)uracil) has been studied in this work. Solvent desorption from samples stored at 95% and 50% relative solvent vapor pressure was studied in isothermal conditions at 30 °C. The results of this study demonstrated that: solvent desorption rate did not differ significantly for both phases; solvent desorption in all cases occurred faster from samples with the largest particle size; and solvent desorption in most cases occurred in two steps. Structure differences and their surface properties were not of great importance on the solvent desorption rates because the main factor affecting desorption rate …

Antimetabolites AntineoplasticVapor PressureChemistry PharmaceuticalInorganic chemistryEthyl acetatePharmaceutical ScienceElectron donorSolventchemistry.chemical_compoundAdsorptionchemistryDesorptionSolventsAdsorptionSolvent effectsAcetonitrileCrystallizationTetrahydrofuranTegafurInternational journal of pharmaceutics
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Dioxygen reduction by cobalt(II) octaethylporphyrin at liquid|liquid interfaces.

2010

Oxygen reduction catalyzed by cobalt(II) (2,3,7,8,12,13,17,18-octaethylporphyrin) [Co(OEP)] at soft interfaces is studied by voltammetry and biphasic reactions. When Co(OEP) is present in a solution of 1,2-dichloroethane in contact with an aqueous acidic solution, oxygen is reduced if the interface is positively polarized (water phase versus organic phase). This reduction reaction is facilitated when an additional electron donor, here ferrocene, is present in excess in the organic phase.

Aqueous solutionPorphyrinsSurface PropertiesInorganic chemistrychemistry.chemical_elementElectron donorOxygenRedoxAtomic and Molecular Physics and OpticsCatalysisCatalysisOxygenchemistry.chemical_compoundchemistryPhase (matter)Organometallic CompoundsPhysical and Theoretical ChemistryCobaltVoltammetryOxidation-ReductionChemphyschem : a European journal of chemical physics and physical chemistry
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Acene-type donors bearing one 1,3-dithiole ring

1999

Abstract A series of acene-type donors bearing only one 1,3-dithiole ring have been synthesized by following a Wittig-Horner reaction from 7 H -benz[ d,e ]anthracen-7-one and several phosphonate esters. The excellent donor properties have been studied using both experimental techniques and quantum-chemical calculations and reveal that the extraction of the first electron in the oxidation process occurs from the dithiole ring (0.42 e) and the acene unit (0.58 e).

Bearing (mechanical)StereochemistryChemistryMechanical EngineeringMetals and AlloysElectron donorCondensed Matter PhysicsRing (chemistry)Chemical synthesisPhosphonateMedicinal chemistryElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundMechanics of MaterialslawMaterials ChemistryMoleculeAceneUnit (ring theory)Synthetic Metals
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Photoluminescence quantum yield exceeding 80% in low dimensional perovskite thin-films via passivation control

2017

Quasi-2D perovskites with the BA : MA molar ratio equal to 3 : 3 show a remarkable PLQY exceeding 80%, thanks to the use of an electron donor as the passivating agent. These films have been applied in LEDs that exhibit high brightness exceeding 1000 cd m−2 and current efficiencies >3 cd A−1.

BrightnessPhotoluminescenceMaterials sciencePassivationQuantum yieldElectron donor02 engineering and technology010402 general chemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundlawMaterials ChemistryThin filmPerovskite (structure)business.industryMetals and AlloysGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesOptoelectronics0210 nano-technologybusinessLight-emitting diodeChemical Communications
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Chemistry and reactivity of dinuclear manganese oxamate complexes: Aerobic catechol oxidation catalyzed by high-valent bis(oxo)-bridged dimanganese(I…

2006

[EN] The high-valent bis(oxo)-bridged dimanganese(IV) complexes with the series of binucleating 4.5-X-2-o-phenylenebis(oxamate) ligands (opbaX(2); X = H, Cl, Me) (1a-c) have been synthesized and characterized structurally, spectroscopically and magnetically. Complexes la-c possess unique Mn-2(mu-O)(2) core structures with two o-phenylenediamidate type additional bridges which lead to exceptionally short Mn-Mn distances (2.63-2.65 angstrom) and fairly bent Mn-O-Mn angles (94.1 degrees-94.6 degrees). The cyclovoltammograms of la-c in acetonitrile (25 degrees C, 0.1 M Bu4NPF6) show an irreversible one-electron oxidation peak at moderately high anodic potentials (E-ap = 0.50-0.85 V versus SCE),…

CatecholManganeseLigandStereochemistryProcess Chemistry and TechnologyCatecholschemistry.chemical_elementElectron donorManganeseMedicinal chemistryCatalysisQuinonechemistry.chemical_compoundHomologous serieschemistryO-O Bond activationOxidationsFISICA APLICADAReactivity (chemistry)Physical and Theoretical ChemistryAcetonitrileRedox properties
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Influence of spatial arrangements of π-spacer and acceptor of phenothiazine based dyes on the performance of dye-sensitized solar cells

2013

Abstract Three phenothiazine based organic dyes PTA , PDTA and PTDA with D– π –A, π –D– π –A and A– π –D– π –A frameworks were designed and synthesized for the dye sensitized solar cells (DSSCs). Phenothiazine with octyloxyphenyl moiety acts as donor while thiophene and cyanoacetic acid units act as a π -spacer and an acceptor, respectively. The effects of the molecular structures of the dyes on the performance of the DSSCs were investigated systematically along with their photophysical and photoelectrochemical properties. The dye PTDA with A– π –D– π –A framework exhibited a better light harvesting capacity and an effective electron extraction pathway from the electron donor to the TiO 2 s…

ChemistryElectron donorGeneral ChemistryCondensed Matter PhysicsPhotochemistryAcceptorElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundDye-sensitized solar cellCyanoacetic acidPhenothiazineOrganic dyeMaterials ChemistryThiopheneMoietyElectrical and Electronic EngineeringOrganic Electronics
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