Search results for "Pyrene"

showing 10 items of 260 documents

Supramolecular assembly of pyrene-tetrathiafulvalene hybrids on graphene: Structure-property relationships and biosensing activity

2021

Two different molecular receptors (1 and 2) incorporating one and three pyrene units to promote the π–π interaction with the basal plane of graphene are reported. In order to modulate the electronic properties of graphene, the new receptors are endowed with an electron-donor tetrathiafulvalene moiety (exTTF). The resulting non-covalent hybrids have been characterized by different analytical, spectroscopic and microscopic techniques (TGA, Raman, UV-Vis absorption, TEM and XPS), and the supramolecular interaction of the molecular systems with graphene has been investigated by theoretical calculations. The electrochemical behavior of the pyrene-exTTF hybrids onto distinct graphene-based materi…

Materials scienceGrapheneSupramolecular chemistryGeneral Chemistrylaw.inventionSupramolecular assemblychemistry.chemical_compoundCrystallographysymbols.namesakechemistrylawMaterials ChemistrysymbolsMoietyPyreneRaman spectroscopyBiosensorTetrathiafulvalene
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Phosphine oxide functionalized pyrenes as efficient blue light emitting multifunctional materials for organic light emitting diodes

2015

In a search for blue light emitting multifunctional materials, the electron transport enhancing diphenyl phosphine–oxide (Ph2PO) group has been appended to blue light emitting pyrene derivatives. This design, we observe, leads to highly efficient electron transporting blue-emitters for non-doped organic light emitting devices (OLEDs) with good film formation characteristics. The superior performance is attributed to enhanced charge transport and formation of pyrene excimers assisted by thermally activated delayed fluorescence (TADF) in the device. We report the synthesis and characterization using experimental and computational methods of six such pyrene derivatives. Although three of these…

Materials scienceQuenching (fluorescence)business.industryStackingGeneral ChemistryPhotochemistryExcimerFluorescencechemistry.chemical_compoundchemistryMaterials ChemistryOLEDOptoelectronicsPyreneThin filmbusinessLuminescenceJournal of Materials Chemistry C
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Photochemical synthesis of pyrene perfluoroalkyl derivatives and their embedding in a polymethylmethacrylate matrix: a spectroscopic and structural s…

2014

A photochemical, alternative and eco-compatible approach to perfluoroalkyl derivatives of pyrene is presented. The perfluoroalkyl chain is regiospecifically introduced at the 1 position of pyrene. The synthesized products have been embedded in a polymethylmethacrylate matrix by photocuring at 365 nm. Both the photochemical reactions can be considered a “green tool” for the synthetic chemist in order to obtain materials with prospective optoelectronic applications. The so-obtained composites have been the object of a study by UV and fluorescence spectroscopy in order to explore their luminescence properties. The small angle X-ray scattering and the transmission electron microscopy techniques…

Materials scienceScatteringGeneral ChemistryMicrostructurePhotochemistryFluorescence spectroscopyPyrene PMMA Photochemical perfluoroalkylation OLEDMatrix (chemical analysis)chemistry.chemical_compoundchemistryTransmission electron microscopyMaterials ChemistryOLEDPyreneLuminescence
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Amphiphilic inulin graft co-polymers as self assembling micelles for doxorubicin delivery

2020

This paper reports the synthesis and characterization of a new amphiphilic inulin graft copolymer able to self-assemble in water into a micelle type structure and to deliver the anticancer model drug doxorubicin. For this aim, inulin was chemically modified in the side chain with primary amine groups (INU-EDA) and these were used as reactive moieties for the conjugation of poly ethylene glycol 2000 and succinyl-ceramide. The CMC of obtained amphiphilic inulin derivatives (INU-ceramide and INU-ceramide-PEG2000) was measured by means of fluorescence analysis using pyrene as the fluorescent probe. The obtained micelles were characterized by DLS and AFM analysis and the ability to release the l…

Materials sciencemicellesInulinBiomedical EngineeringMicelledoxorubicinchemistry.chemical_compoundPolymer chemistryAmphiphileCopolymermedicineSide chainGeneral Materials ScienceDoxorubicininulin micelles drug delivery doxorubicin graft co-polymersgraft co-polymersinulinGeneral ChemistryGeneral MedicinechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliverydrug deliveryPyrenemedicine.druginulin; micelles; drug delivery; doxorubicin; graft co-polymers
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O-Doped Nanographenes: A Pyrano/Pyrylium Route Towards Semiconducting Cationic Mixed-Valence Complexes

2020

Herein we report an efficient synthesis to prepare O‐doped nanographenes, which derive from the longitudinally and latitudinally p‐extension of pyrene. The derivatives are highly fluorescent and feature low‐oxidation potentials. Exploiting electrooxidation, crystals of cationic mixed valence (MV) complexes were grown in which the organic salts organize into face‐to‐face p‐ p stacks, a favorable solid‐state arrangement for organic electronics. Variable‐temperature EPR measurements and relaxation studies suggest a strong electron delocalization along the longitudinal axis of the columnar p‐stacking architectures. Electric measurements of single crystals of the MV salts exhibited a semiconduct…

Materials sciencemolecular graphenespolycyclic aromatic hydrocarbonsHeteroatom010402 general chemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundCompostos orgànicslaw[CHIM]Chemical ScienceselectrocrystallizationElectron paramagnetic resonanceOrganic electronicsValence (chemistry)[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryDopingCationic polymerizationGeneral MedicineGeneral Chemistryelectrocrystallization; electron paramagnetic resonance; heteroatom doping; molecular graphenes; polycyclic aromatic hydrocarbonsFluorescence0104 chemical sciencesElectroquímicaCrystallographyelectron paramagnetic resonancechemistryPyreneheteroatom doping
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Characterization of cryopreserved rat liver parenchymal cells by metabolism of diagnostic substrates and activities of related enzymes

1992

The metabolism of testosterone and benzo(a)pyrene (BaP) which is mediated by diverse enzymes was determined in cryopreserved rat liver parenchymal cells and compared with that found in freshly isolated cells. In addition, the activities of single xenobiotic-metabolizing enzymes were measured by using specific substrates. The cytochrome P450 (P450)-mediated total metabolic conversion of testosterone was reduced to 55% in cryopreserved cells. The metabolite profile, i.e. the formation of single metabolites compared with total metabolic conversion, was however unchanged when compared with freshly isolated cells. A concomitant reduction in the activities of the involved P450 isoenzymes can ther…

MetaboliteCell CountBiologyHydroxylationBiochemistryIsozymeCryopreservationchemistry.chemical_compoundCytochrome P-450 Enzyme SystemBenzo(a)pyreneAnimalsTestosteroneGlutathione TransferaseCryopreservationPharmacologyProteinsCytochrome P450Trypan BlueMetabolismArylsulfotransferaseRatsLiverchemistryBiochemistryCell culturebiology.proteinPercollDrug metabolismBiochemical Pharmacology
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Unzipping Nucleoside Channels by Means of Alcohol Disassembly

2013

Gold nanoparticles capped with simple adenosine derivatives can form colloidal aggregates in nonpolar solvents. Theoretical calculations indicate the formation of organic channels by the supramolecular assembly of the nanoparticles by means of hydrogen bonds between the adenine moieties. The aggregates were only negligibly sensitive to nPrOH, iPrOH, and tBuOH, whereas some showed a similar response to MeOH and EtOH, and others showed high selectivity toward MeOH. DNA nucleoside derivatives (1-(2-deoxy-β-D-ribofuranosyl)-5-methyluracil and 2′,3′-O-isopropylideneadenosine) as well as thymine and other aromatic compounds such as pyrene derivatives (pyrene, 1-chloropyrene, 1-hydroxypyrene, (1-p…

Metal NanoparticlesNanoparticlePhotochemistryCatalysisSupramolecular assemblychemistry.chemical_compoundBase PairingChemistryHydrogen bondOtras Ciencias QuímicasOrganic ChemistryCiencias QuímicasHydrogen BondingNucleosidesDNAGeneral ChemistryCombinatorial chemistryThymineColloidal goldAlcoholsRNANanoparticlesPyreneGoldNucleosideCIENCIAS NATURALES Y EXACTASDNAChemistry - A European Journal
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Blue-emitting pyrene-based aggregates.

2015

The self-assembling features and gel formation of two pyrene imidazoles are presented. The supramolecular aggregation of these synthesised molecules results in an unusual blue-monomeric emission, which is rationalized by a combined experimental and theoretical investigation.

Metals and AlloysSupramolecular chemistrymacromolecular substancesGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMonomerchemistryPolymerizationMaterials ChemistryCeramics and CompositesBlue emittingPyreneChemical communications (Cambridge, England)
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Glutathione Conjugation of Bay- and Fjord-Region Diol Epoxides of Polycyclic Aromatic Hydrocarbons by Glutathione Transferases M1-1 and P1-1

1997

Metabolism of polycyclic aromatic hydrocarbons in mammalian cells results in the formation of vicinal diol epoxides considered as ultimate carcinogens if the oxirane ring is located in a bay- or fjord-region of the parent compound. In the present study, individual stereoisomers of the bay-region diol epoxides of chrysene, dibenz[a,h]anthracene, and benzo[a]pyrene as well as of the fjord-region diol epoxides of benzo[c]phenanthrene, benzo[c]chrysene, and benzo[g]-chrysene have been incubated with GSH in the presence of human glutathione transferases GSTM1-1 (a mu-class enzyme) and GSTP1-1 (a pi-class enzyme). As previously shown with GSTA1-1 (an alpha-class enzyme) both M1-1 and P1-1 demonst…

Models MolecularChryseneStereochemistryConjugated systemToxicologySubstrate Specificitychemistry.chemical_compoundpolycyclic compoundsHumansPolycyclic Aromatic HydrocarbonsCarcinogenGlutathione TransferaseBay-Region Polycyclic Aromatic Hydrocarbonchemistry.chemical_classificationAnthraceneintegumentary systemStereoisomerismGeneral MedicineGlutathionePhenanthreneGlutathioneIsoenzymesKineticsEnzymechemistryCarcinogensEpoxy CompoundsPyreneCrystallizationChemical Research in Toxicology
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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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