Search results for "Fluorene"

showing 10 items of 82 documents

Synthesis of phenothiazine-based di-anchoring dyes containing fluorene linker and their photovoltaic performance

2015

Abstract A new di-anchoring organic dye based on phenothiazine featuring A-D-π-D-A (acceptor-donor-π-linker-donor-acceptor) configuration with fluorene as the π linker was designed and successfully synthesized. Compared to the corresponding mono-anchoring D-A congener, this new dye exhibited a broader and stronger absorption in the light wavelength ranging from 400 nm to 600 nm and thus showed a more efficient photovoltaic performance for dye-sensitized solar cells (DSSCs). The overall power conversion efficiency (η) of this new dye in a sensitized solar cell amounted to 5.70%, which is 17% higher than that of the equivalent based counterpart (4.87%). On the other hand, the introduction of …

Materials scienceProcess Chemistry and TechnologyGeneral Chemical EngineeringEnergy conversion efficiencyFluoreneMolar absorptivityPhotochemistrylaw.inventionDye-sensitized solar cellchemistry.chemical_compoundchemistrylawPhenothiazineSolar cellThiopheneLinkerDyes and Pigments
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Redox-responsive organometallic foldamers from ferrocene amino acid: Solid-phase synthesis, secondary structure and mixed-valence properties

2011

Oligoferrocenes Fmoc-Fca(n)-OMe (n=3-5) are assembled in a stepwise precise manner from Fmoc-protected ferrocene amino acid Fmoc-Fca-OH (H-Fca-OH = 1-amino-1'-ferrocene carboxylic acid; Fmoc = 9-fluorenylmethyloxycarbonyl) via amide bonds on solid supports by sequential Fmoc deprotection, acid activation and coupling steps. The resulting well-defined oligomers form ordered zigzag structures in THF solution with characteristic hydrogen bonding patterns. Electrochemical experiments reveal sequential oxidations of the individual ferrocene units in these peptides giving mixed-valent cations. Optical intervalence electron transfer is detected by intervalence transitions in the near-IR.

Models MolecularMetallocenesStereochemistryCarboxylic acidProtein Structure SecondaryInorganic Chemistrychemistry.chemical_compoundElectron transferSolid-phase synthesisPolymer chemistryOrganometallic CompoundsFerrous CompoundsAmino AcidsProtein secondary structurechemistry.chemical_classificationFluorenesValence (chemistry)Hydrogen bondSpectrum AnalysisDipeptidesAmino acidSolutionschemistryFerrocenePeptidomimeticsOxidation-ReductionDalton Transactions
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Uridine uptake inhibition as a cytotoxicity test for a human hepatoma cell line (HepG2 cells): comparison with the neutral red assay

2001

International audience; This study describes a sensitive microassay for measuring cytotoxicity based on the degree of inhibition of RNA synthesis in HepG2 cells. RNA synthesis is measured by the kinetic uptake of radiolabeled uridine. A large number of compounds were tested in a wide range of concentrations. The concentration required to induce 50% inhibition of HepG2 uridine uptake rates (IC50) was determined for each compound and used to rank its potency. These IC50s were compared with IC50s measured with the neutral red assay. 2-acetylaminofluorene, benzo[a]pyrene and methylnitrosourea were not cytotoxic in the neutral red assay. Uridine uptake was always inhibited at lower concentrations…

Neutral redCarcinoma Hepatocellular[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainToxicologyXenobiotics03 medical and health scienceschemistry.chemical_compoundInhibitory Concentration 500302 clinical medicineNeutral redToxicity TestsTumor Cells CulturedPotencyCytotoxic T cellHumansBenzopyrenesCytotoxicityColoring AgentsUridine030304 developmental biology0303 health sciencesReproducibility of ResultsMethylnitrosourea2-AcetylaminofluoreneUridine uptakeIn vitroUridineKineticschemistryBiochemistryCytotoxicity-helpG2 cell line[SDV.TOX.TCA] Life Sciences [q-bio]/Toxicology/Toxicology and food chain030220 oncology & carcinogenesisToxicityCarcinogensHepatocytesPyreneRNARegression AnalysisWater Pollutants Chemical
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The Interplay of Inverted Redox Potentials and Aromaticity in the Oxidized States of New π-Electron Donors: 9-(1,3-Dithiol-2-ylidene)fluorene and 9-(…

2006

Derivatives of 9-(1,3-dithiol-2-ylidene)fluorene (9) and 9-(1,3-dithiol-2-ylidene)thioxanthene (10) have been synthesised using Horner-Wadsworth-Emmons reactions of (1,3-dithiol-2-yl)phosphonate reagents with fluorenone and thioxanthen-9-one. X-ray crystallography, solution electrochemistry, optical spectroscopy, spectroelectrochemistry and simultaneous electrochemistry and electron paramagnetic resonance (SEEPR), combined with theoretical calculations performed at the B3P86/6-31G** level, elucidate the interplay of the electronic and structural properties in these molecules. These compounds are strong two-electron donors, and the oxidation potentials depend on the electronic structure of t…

Organic ChemistryThioxantheneDithiolAromaticitySulfoxideGeneral ChemistryFluorenePhotochemistryCatalysisDicationchemistry.chemical_compoundchemistryFluorenoneRadical ionChemistry - A European Journal
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Exposure to retene, fluoranthene, and their binary mixture causes distinct transcriptomic and apical outcomes in rainbow trout (Oncorhynchus mykiss) …

2022

Polycyclic aromatic hydrocarbons (PAHs) are widely spread environmental contaminants which affect developing organisms. It is known that improper activation of the aryl hydrocarbon receptor (AhR) by some PAHs contributes to toxicity, while other PAHs can disrupt cellular membrane function. The exact downstream mechanisms of AhR activation remain unresolved, especially with regard to cardiotoxicity. By exposing newly hatched rainbow trout alevins (Oncorhynchus mykiss) semi-statically to retene (32 µg l−1; AhR agonist), fluoranthene (50 µg l−1; weak AhR agonist and CYP1a inhibitor) and their binary mixture for 1, 3, 7 and 14 days, we aimed to uncover novel mechanisms of cardiotoxicity using a…

PAH-yhdisteetFluorenesEarly life developmentHealth Toxicology and MutagenesisPAHPhenanthrenesAquatic ScienceseoksetReteneekotoksikologiakirjolohiOncorhynchus mykissMixtureAnimalsFluorantheneympäristömyrkytalkionkehitystranskriptomiPolycyclic Aromatic HydrocarbonsTranscriptomeWater Pollutants ChemicalYolk Sac
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Boron–nitrogen substituted dihydroindeno[1,2-b]fluorene derivatives as acceptors in organic solar cells

2019

The electrophilic borylation of 2,5-diarylpyrazines results in the formation of boron–nitrogen doped dihydroindeno[1,2-b]fluorene which can be synthesized using standard Schlenk techniques and worked up and handled readily under atmospheric conditions. Through transmetallation via diarylzinc reagents a series of derivatives were synthesized which show broad visible to near-IR light absorption profiles that highlight the versatility of this BN substituted core for use in optoelectronic devices. The synthesis is efficient, scalable and allows for tuning through changes in substituents on the planar heterocyclic core and at boron. Exploratory evaluation in organic solar cell devices as non-ful…

PAH-yhdisteetMaterials scienceOrganic solar cellchemistry.chemical_elementFluoreneOrganoboron chemistry010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesBorylationCatalysischemistry.chemical_compoundTransmetalationMaterials ChemistryBoronaurinkokennot010405 organic chemistryDopingMetals and AlloysGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryElectrophileCeramics and CompositesvalokemiaChemical Communications
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Changes in Cardiac Proteome and Metabolome Following Exposure to the Pahs Retene and Fluoranthene and Their Mixture in Developing Rainbow Trout Alevi…

2022

Exposure to polycyclic aromatic hydrocarbons (PAHs) is known to affect developing organisms. Utilization of different omics-based technologies and approaches could therefore provide a base for the discovery of novel mechanisms of PAH induced development of toxicity. To this aim, we investigated how exposure towards two PAHs with different toxicity mechanisms: retene (an aryl hydrocarbon receptor 2 (Ahr2) agonist), and fluoranthene (a weak Ahr2 agonist and cytochrome P450 inhibitor (Cyp1a)), either alone or as a mixture, affected the cardiac proteome and metabolome in newly hatched rainbow trout alevins (Oncorhynchus mykiss). In total, we identified 65 and 82 differently expressed proteins (…

PAH-yhdisteetProteomicsHistoryEnvironmental EngineeringProteomePolymers and PlasticsDevelopmental toxicologyPharmacology and ToxicologyZoologiproteomiikkaIndustrial and Manufacturing EngineeringkirjolohiMixtureAnimalsEnvironmental ChemistryMetabolomicsPolycyclic Aromatic HydrocarbonsBusiness and International ManagementaineenvaihduntaWaste Management and DisposalFluorenessydänPAHPhenanthrenesFarmakologi och toxikologiMiljövetenskapPollutionekotoksikologiaRainbow troutOncorhynchus mykissMetabolomePROTEOMICSkehitysbiologiaZoologyEnvironmental SciencesSSRN Electronic Journal
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Solid-Phase Synthesis of Peptide Libraries Combining α-Amino Acids with Inorganic and Organic Chromophores

2009

The synthesis of two series of peptidic chains composed of bis(terpyridine)ruthenium(II) acceptor units and organic chromophores (coumarin, naphthalene, anthracene, fluorene) by stepwise solid-phase peptide synthesis (SPPS) techniques is described. The first series of dyads comprises directly amide linked chromophores, while the second one possesses a glycine spacer between the two chromophores. All dyads were studied by UV/Vis and NMR spectroscopy, steady-state luminescence, luminescence decay and electrochemistry, as well as by DFT calculations. The results of these studies indicate weak electronic coupling of the chromophores in the ground state. Absorption spectra of all dyads are domin…

Photochemistrychemistry.chemical_elementNaphthalenesFluorenePhotochemistryRutheniumCatalysischemistry.chemical_compoundCoumarinsPeptide LibraryElectrochemistryAmino AcidsColoring AgentsAnthracenesFluorenesAnthraceneQuenching (fluorescence)Spectrum AnalysisOrganic ChemistryGeneral ChemistryNuclear magnetic resonance spectroscopyChromophoreRutheniumchemistryTerpyridinePeptidesLuminescenceChemistry - A European Journal
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The influence of automobile exhausts on mutagenicity of soils: contamination with, fractionation, separation, and preliminary identification of mutag…

2000

To test the assumption that automobile exhausts contribute to soil mutagenicity, two soils with low levels of mutagenic activities were exposed to traffic exhausts at a heavily charged junction of German motorways (Autobahnen) for 3, 7, 10, 13, 17, 21, and 26 weeks. Indeed, in the presence of a metabolic activation system from rat liver (S9), an average increase of 8 and 9 (4 and 12) revertants per gram per week was found in Salmonella typhimurium TA 98 (TA 100). In the absence of S9, meaningful measurements were impossible on account of a concurrent dose dependent increase of toxicity. No correlation between the increase of mutagenicity and the contents of polycyclic aromatic hydrocarbons …

Salmonella typhimuriumHealth Toxicology and MutagenesisSister chromatid exchangeMutagenBone Marrow CellsFractionationmedicine.disease_causeAmes testchemistry.chemical_compoundMiceGermanyGeneticsmedicineAnimalsHumansSoil PollutantsLymphocytesPolycyclic Aromatic HydrocarbonsBiotransformationCells CulturedVehicle EmissionsFluorenesChromatographyMicronucleus TestsPyrenesMutagenicity TestsTolueneRatsSolventchemistryMicronucleus testMicrosomes LiverSolventsPyreneSister Chromatid ExchangeMutagensMutation research
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Inhibition of the mutagenicity of 2-nitrofluorene, 3-nitrofluoranthene and 1-nitropyrene by vitamins, porphyrins and related compounds, and vegetable…

1997

When 21 vitamins including related compounds haemin, chlorophyllin, chlorophyll, biliverdin and bilirubin, as well as juices from five fruits and 25 vegetables and solvent extracts from the residues of fruits and vegetables were tested for their antimutagenic potencies with respect to mutagenicity induced by 2-nitrofluorene (2-NF), 3-nitrofluoranthene (3-NFA) and 1-nitropyrene(1-NP) in Salmonella typhimurium TA98 the following results were obtained. The tetracyclic nitroarenes 3-NFA and 1-NP were in general more effectively antagonized by potent antimutagenic compounds than the tricyclic 2-NF. beta-Carotene, retinol, retinal, retinoic acid, retinol palmitate, riboflavin 5'-phosphate, alpha-…

Salmonella typhimuriumPorphyrinsBilirubinMutagenToxicologymedicine.disease_causechemistry.chemical_compoundbeta-CaroteneVegetablesmedicineFood scienceCarotenoidchemistry.chemical_classificationFluorenesPyrenesBiliverdinMutagenicity TestsChlorophyllinfood and beveragesAntimutagenic AgentsVitaminsGeneral MedicinechemistryBiochemistryAntimutagenic AgentsFruitSolventsAntimutagenMutagensFood ScienceFood and Chemical Toxicology
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