Search results for "ANTHRACENE"

showing 10 items of 171 documents

Pressure-Induced Polymerization of Polycyclic Arene-Perfluoroarene Cocrystals: Single Crystal X-ray Diffraction Studies, Reaction Kinetics, and Desig…

2020

Pressure-induced polymerization of aromatic compounds leads to novel materials containing sp3 carbon-bonded networks. The choice of the molecular species and the control of their arrangement in the crystal structures via intermolecular interactions, such as the arene–perfluoroarene interaction, can enable the design of target polymers. We have investigated the crystal structure compression and pressure-induced polymerization reaction kinetics of two polycyclic 1:1 arene–perfluoroarene cocrystals, naphthalene/octafluoronaphthalene (NOFN) and anthracene/octafluoronaphthalene (AOFN), up to 25 and 30 GPa, respectively, using single-crystal synchrotron X-ray diffraction, infrared spectroscopy, a…

chemistry.chemical_classificationAnthraceneStackingInfrared spectroscopyGeneral ChemistryPolymerCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographyColloid and Surface ChemistryPressure-induced polymerization; single-crystal synchrotron X-ray diffraction; high-pressure kinetic studychemistryPolymerizationX-ray crystallographySingle crystal
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A study of weathered coal spectroscopic properties

2017

Abstract Current coal industry causes significant environmental pollution and the most air pollution deaths in the world, making the development of new eco-friendly applications one of the top priorities. Coal contains up to 50 % humic substances (HS), the majority of which is humic acid (HA). HA is well known for its beneficial properties and thus compounds extracted from coal can be used to develop new applications. To address this issue, we assessed structural composition of coal HS by measuring their spectroscopic properties. As the result, obtained spectra can be used to identify information about the molecules and thus allowing describing the composition of HS. The purpose of this stu…

chemistry.chemical_classificationAnthracenebusiness.industry020209 energyAir pollutionEnvironmental pollutionWeathering02 engineering and technology010501 environmental sciencesmedicine.disease_causecomplex mixtures01 natural scienceschemistry.chemical_compoundchemistryEnvironmental chemistryAcridine0202 electrical engineering electronic engineering information engineeringmedicineOrganic chemistryHumic acidCoalbusiness0105 earth and related environmental sciencesNaphthaleneEnergy Procedia
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Purification of rat liver epoxide hydratase to apparent homogeneity.

1975

Epoxide hydratase (EC 4.2.1.63) is a microsomal enzyme which catalyses the conversion of epoxides to trans-dihydrodiols. Epoxides, produced by the action of microsomal monooxygenases (EC 1.14.1.1) from aromatic and olefinic compounds, are thought to be responsible for many of the harinful effects of polycyclic hydrocarbons and related compounds. Thus epoxide hydratase, together with glutathione 9transferases, (EC 2.5.1.18) may play an important role in the removal of carcinogenic and cytotoxic metabolites (for reviews see [l-3]). It has been reported [4,5] that dihydrodiols formed from some polycyclic hydrocarbons (benz(a)anthracene and benzo(a)pyrene) are reactivated by the microsomal mono…

chemistry.chemical_classificationEpoxide HydrolasesMaleAnthraceneBiophysicsCell BiologyGlutathioneMonooxygenaseBiochemistryRatsMolecular Weightchemistry.chemical_compoundEnzymechemistryBiochemistryStructural BiologyGeneticsMicrosomeMicrosomes LiverPyreneAnimalsPolycyclic HydrocarbonsMolecular BiologyCarcinogenHydro-LyasesFEBS letters
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A new cross-linkable 9,10-diphenylanthracene derivative as a wide bandgap host for solution-processed organic light-emitting diodes

2018

Efficient organic light-emitting diodes (OLEDs) can be obtained using multilayered architectures where the processes of charge injection, transport and recombination are separated and optimized in each layer. Processing these structures from solution requires strategies to avoid redissolution or damage of the previously deposited layers. Several reports have demonstrated the development of cross-linkable hole transport materials, while less literature describes the synthesis and applications of such wide bandgap host materials for multilayered OLEDs. In this work we introduce a cross-linkable derivative of 9-(4-(10-phenylanthracene-9-yl)phenyl)-9H-carbazole incorporating styrene moieties (S…

chemistry.chemical_classificationMaterials sciencebusiness.industryBand gapRadical polymerization910-Diphenylanthracene02 engineering and technologyGeneral ChemistryPolymerElectroluminescence010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryMaterials ChemistryOLEDOptoelectronics0210 nano-technologybusinessLayer (electronics)DiodeJournal of Materials Chemistry C
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Luminescence properties of a cofacial dipalladium porphyrin dimer under argon and in the presence of dioxygen

2001

The preparation and luminescence properties of a dipalladium cofacial porphyrin dimer (DPA) Pd 2 (where DPA is the tetraanion of 1,8-bis(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrin-5-yl)anthracene) are reported and compared together with the photophysical behavior of the known monomeric (OEP)Pd and (TPP)Pd complexes. The effect of dioxygen in the presence and in the absence of the very bulky base, 1-t-butyl-5-phenylimidazole, is also investigated. The title dimer, (DPA) Pd 2, shows fluorescence and phosphorescence in the ps and ms time scale, respectively, with a global intensity lower than that of the porphyrin monomer analogues. The fluorescence sensitivity towards dioxygen quenc…

chemistry.chemical_compoundAnthraceneQuenching (fluorescence)MonomerchemistryDimerGeneral ChemistryLuminescencePhotochemistryPhosphorescenceFluorescencePorphyrinJournal of Porphyrins and Phthalocyanines
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Isolation, separation and quantification of metabolites of the carcinogenic polycyclic aromatic hydrocarbon dibenz(a,h)anthracene

1986

chemistry.chemical_compoundCarcinogenic Polycyclic Aromatic HydrocarbonChemistryClinical BiochemistryOrganic chemistryDibenz(ah)anthraceneGeneral Materials ScienceGeneral MedicineIsolation (microbiology)Analytical ChemistryFresenius' Zeitschrift für analytische Chemie
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Controlling Spin-Correlated Radical Pairs with Donor-Acceptor Dyads: A New Concept to Generate Reduced Metal Complexes for More Efficient Photocataly…

2021

Abstract One‐electron reduced metal complexes derived from photoactive ruthenium or iridium complexes are important intermediates for substrate activation steps in photoredox catalysis and for the photocatalytic generation of solar fuels. However, owing to the heavy atom effect, direct photochemical pathways to these key intermediates suffer from intrinsic efficiency problems resulting from rapid geminate recombination of radical pairs within the so‐called solvent cage. In this study, we prepared and investigated molecular dyads capable of producing reduced metal complexes via an indirect pathway relying on a sequence of energy and electron transfer processes between a Ru complex and a cova…

chemistry.chemical_element010402 general chemistryPhotochemistry7. Clean energy01 natural sciencestime-resolved spectroscopyCatalysischemistry.chemical_compoundElectron transferBipyridineMoietyPhotochemistry | Hot Paperdonor–acceptor systemsenergy transferAnthraceneFull Paper010405 organic chemistryOrganic ChemistryPhotoredox catalysisGeneral ChemistryFull Paperselectron transfer0104 chemical sciencesRutheniumchemistryPhotocatalysisFlash photolysisphotocatalysis
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Open-chain polyamine ligands bearing an anthracene unit - Chemosensors for logic operations at the molecular level

2001

In this work the absorption and the fluorescence emission properties as well as the protonation sequence of three open chain polyamine ligands of different dimensions bearing an anthracene unit were studied. The protonation and stability constants with Ni2+, Cu2+, Zn2+, and Cd2+ have been determined in 0.15 mol·dm−3 NaCl at 298.1 ± 0.1 K. The values of both protonation and stability constants follow the expected trends according to the number of nitrogen donors, sequence of chelate rings and hydrophilic−hydrophobic balance. Chelation enhancement of the fluorescence emission (CHEF) was observed for some complexes of these ligands with Zn2+ and Cd2+. In contrast the analog complexes containin…

inorganic chemicalsAnthraceneQuenching (fluorescence)Inorganic chemistrychemistry.chemical_elementProtonationFluorescenceCopperInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artvisual_art.visual_art_mediumChelationAbsorption (chemistry)
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Skin response to a carcinogen involves the xenobiotic receptor pregnane X receptor.

2015

Skin is in daily contact with potentially harmful molecules from the environment such as cigarette smoke, automobile emissions, industrial soot and groundwater. Pregnane X receptor (PXR) is a transcription factor expressed in liver and intestine that is activated by xenobiotic chemicals including drugs and environmental pollutants. Topical application of the tumor initiator 7,12-dimethylbenz(a)anthracene (DMBA) enhances Pxr, Cyp1a1, Cyp1b1 and Cyp3a11, but not Ahr expression in the skin. Surprisingly, DMBA-induced Pxr upregulation is largely impaired in Langerin(+) cell-depleted skin, suggesting that DMBA mainly triggers Pxr in Langerin(+) cells. Furthermore, PXR deficiency protects from DN…

medicine.medical_specialtyReceptors SteroidLangerinDNA damage910-Dimethyl-12-benzanthraceneDMBADermatologymedicine.disease_causeBiochemistrydigestive systemArticleDownregulation and upregulationCell MovementInternal medicinemedicineAnimalsMolecular BiologyCarcinogenSkinPregnane X receptorbiologyintegumentary systemPregnane X ReceptorAryl hydrocarbon receptordigestive system diseasesUp-RegulationMice Inbred C57BLEndocrinologyLangerhans CellsCancer researchbiology.proteinCarcinogensCarcinogenesisDNA DamageExperimental dermatology
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Donor-π-acceptors containing the 10-(1,3-dithiol-2-ylidene)anthracene unit for dye-sensitized solar cells

2012

Two donor-acceptor molecular tweezers incorporating the 10-(1,3-dithiol-2-ylidene)anthracene unit as donor group and two cyanoacrylic units as accepting/anchoring groups are reported as metal-free sensitizers for dye-sensitized solar cells. By changing the phenyl spacer with 3,4-ethylenedioxythiophene (EDOT) units, the absorption spectrum of the sensitizer is red-shifted with a corresponding increase in the molar absorptivity. Density functional calculations confirmed the intramolecular charge-transfer nature of the lowest-energy absorption bands. The new dyes are highly distorted from planarity and are bound to the TiO(2) surface through the two anchoring groups in a unidentate binding for…

optical propertiesAbsorption spectroscopypigments010402 general chemistryPhotochemistrydyes01 natural sciences7. Clean energyCatalysischemistry.chemical_compound[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUSAnthracene010405 organic chemistryOrganic ChemistryDithiolGeneral ChemistryMolar absorptivity0104 chemical sciencesDye-sensitized solar cellchemistryIntramolecular forcesensitizerssolar cellsAbsorption (chemistry)absorptionMolecular tweezers
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