Search results for "ANTHRACENE"

showing 10 items of 171 documents

Novel Alkylanthracenes Synthesis, Reductive Alkylation, and Reductive Polymerization

1988

A series of novel substituted anthracenes has been prepared which carry two or four n-alkyl groups at C-2 and C-3 (C-6 and C-7). The route taken includes the synthesis of novel 2,3-dialkylbutadienes, their Diels-Alder reaction with 1,4-benzo- or 1,4-naphthoquinone, the dehydrogenation of the adducts, and the reduction of the anthraquinones. The substituted anthracenes are submitted to reduction and reductive alkylation in ethereal solvents and in liquid ammonia to yield 9,10-dialkyl-substituted 9,10-dihydroanthracenes. A modification of the reductive alkylation, i.e. the introduction of 1,n-dihaloalkanes as electrophiles, provides polymeric chains, in which dihydroanthracene moieties are li…

Inorganic ChemistryEnd-groupAnthracenechemistry.chemical_compoundPolymerizationChemistryStereochemistryElectrophileAlkylationMedicinal chemistryAdductQuinoneCarbanionChemische Berichte
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Radioactively labelled epoxides. part V. Tritium labelled K-region oxides and trans-dihydrodiols of pyrene, benzo[a]pyrene and dibenz[a, h]anthracene

1987

Tritium labelled K-region oxides of pyrene, benzo[a]pyrene and dibenz[a,h]anthracene have been prepared by cyclization of the corresponding trans-dihydrodiols which were obtained by reduction of K-region quinones with sodium borotritide in the presence of oxygen. This synthetic pathway not only yields two metabolically important radioactively labelled derivatives of polycyclic aromatic hydrocarbons in a simple and efficient manner, but also requires a rather inexpensive source of tritium.

AnthraceneOrganic Chemistrychemistry.chemical_elementBiochemistryMedicinal chemistryOxygenAnalytical Chemistrychemistry.chemical_compoundchemistryBenzo(a)pyreneDrug Discoverypolycyclic compoundsDibenz(ah)anthracenePyreneOrganic chemistryRadiology Nuclear Medicine and imagingTritiumSpectroscopySodium borotritideJournal of Labelled Compounds and Radiopharmaceuticals
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Arbuscular mycorrhizal fungi altered the hypericin, pseudohypericin, and hyperforin content in flowers of Hypericum perforatum grown under contrastin…

2016

St. John's Wort (Hypericum perforatum) is a perennial herb able to produce water-soluble active ingredients (a.i.), mostly in flowers, with a wide range of medicinal and biotechnological uses. However, information about the ability of arbuscular mycorrhizal fungi (AMF) to affect its biomass accumulation, flower production, and concentration of a.i. under contrasting nutrient availability is still scarce. In the present experiment, we evaluated the role of AMF on growth, flower production, and concentration of bioactive secondary metabolites (hypericin, pseudohypericin, and hyperforin) of H. perforatum under contrasting P availability. AMF stimulated the production of aboveground biomass und…

0106 biological sciencesBiomassPlant Science01 natural scienceschemistry.chemical_compoundNutrientGuttiferae sensu lato; Hypericaceae; Naphthodianthrones; Phenols; Phloroglucinols; St. John’s Wort; Flowers; Hypericum; Mycorrhizae; Perylene; Phloroglucinol; Phosphorus; Plant Extracts; TerpenesMycorrhizaeGuttiferae sensu latoPerylenemedia_commonAnthracenesbiologyNaphthodianthronefood and beveragesHypericum perforatumPhosphorus04 agricultural and veterinary sciencesGeneral MedicineHypericinSettore AGR/02 - Agronomia E Coltivazioni ErbaceeHypericumHypericummedicine.drugmedia_common.quotation_subjectFlowersSecondary metabolitePhloroglucinolCompetition (biology)GeneticPhenolsBotanyGeneticsmedicinePhloroglucinolsGuttiferae sensu lato; Hypericaceae; Naphthodianthrones; Phenols; Phloroglucinols; St. John’s Wort; Ecology Evolution Behavior and Systematics; Molecular Biology; Genetics; Plant ScienceMolecular BiologyEcology Evolution Behavior and SystematicsPhenolPlant ExtractsTerpenesfungiHypericaceaebiology.organism_classificationEcology Evolution Behavior and SystematicHyperforinchemistry040103 agronomy & agriculture0401 agriculture forestry and fisheriesNaphthodianthronesSt. John’s Wort010606 plant biology & botany
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Unexpected DNA damage caused by polycyclic aromatic hydrocarbons under standard laboratory conditions

2007

Abstract The genotoxicity of 15 polycyclic aromatic hydrocarbons was determined with the alkaline version of the comet assay employing V79 lung fibroblasts of the Chinese hamster as target cells. These cells lack the enzymes necessary to convert PAHs to DNA-binding metabolites. Surprisingly, 11 PAHs, i.e., benzo[ a ]pyrene (BaP), benz[ a ]anthracene, 7,12-dimethylbenz[ a ]anthracene, 3-methylcholanthrene, fluoranthene, anthanthrene, 11 H -benzo[ b ]fluorene, dibenz[ a,h ]anthracene, pyrene, benzo[ ghi ]perylene and benzo[ e ]pyrene caused DNA strand breaks even without external metabolic activation, while naphthalene, anthracene, phenanthrene and naphthacene were inactive. When the comet as…

LightHealth Toxicology and MutagenesisAnthanthreneFluorenemedicine.disease_causeMedicinal chemistrychemistry.chemical_compoundCricetulusCricetinaeCytochrome P-450 CYP1A1polycyclic compoundsGeneticsmedicineAnimalsPolycyclic Aromatic HydrocarbonsBiotransformationCells CulturedFluorantheneAnthracenePhenanthreneComet assaychemistryPyreneComet AssayGenotoxicityDNA DamageMutation Research/Genetic Toxicology and Environmental Mutagenesis
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Dendron to central core S1-S1 and S2-S(n) (n1) energy transfers in artificial special pairs containing dendrimers with limited numbers of conformatio…

2013

Two dendrimers consisting of a cofacial free-base bisporphyrin held by a biphenylene spacer and function- alized with 4-benzeneoxomethane (5-(4-benzene)tri-10,15,20-(4-n-octyl- benzene)zinc(II)porphyrin) using either five or six of the six available meso-positions, have been synthesized and characterized as models for the an- tenna effect in Photosystems I and II. The presence of the short linkers, -CH2O-, and long C8H17 soluble side chains substantially reduces the number of conformers (foldamers) compared with classic dendrimers built with longer flexible chains. This simpli- fication assists in their spectroscopic and photophysical analysis, notably with respect to fluorescence resonance…

AnthracenesDendrimersMolecular StructureStereochemistryMetalloporphyrinsOrganic ChemistryGeneral ChemistryBiphenylenePorphyrinFluorescenceAcceptorCatalysischemistry.chemical_compoundCrystallographyFörster resonance energy transferchemistryEnergy TransferModels ChemicalDendrimerSinglet stateConformational isomerismChemistry (Weinheim an der Bergstrasse, Germany)
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Metabolism of Phenanthrene, Benz[a]anthracene, Benzo[a]pyrene, Chrysene and Benzo[c]phenanthrene by Eight cDNA-expressed Human and Rat Cytochromes P4…

1996

Abstract Phenanthrene, benz[a]anthracene, chrysene, benzo[c]phenanthrene, and benzo[a]pyrene have been studied for their regiospecific oxidation by five human (1A1, 1A2, 2A6, 2E1, 3A4) and three rat (1A1, 1A2, 2B1) CYP isoforms. All substrates are preferentially metabolized by CYP1A1 and CYP1A2 in human and rat. Other isoforms play a minor role if at all. Significant differences between human and rat CYP isoforms can be recognized with regard to the regiospecific oxidation of PAH. For instance, K-region oxidation is more pronounced in rat than in human CYP1A1 and CYP1A2. Hence, extrapolation from metabolism studies in rodents to human may be limited.

ChryseneAnthracenePolymers and PlasticsStereochemistryOrganic ChemistryBenzo(c)phenanthreneCYP1A2respiratory systemPhenanthreneBenz(a)anthracenechemistry.chemical_compoundBenzo(a)pyrenechemistrypolycyclic compoundsMaterials ChemistryPyreneheterocyclic compoundsPolycyclic Aromatic Compounds
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The use of anthracene as a model compound in a comparative study of hydrous pyrolysis methods for industrial waste remediation

2011

Author's version of an article published in Chemosphere, 84 (4), 403-408. Also available from the publisher: http://dx.doi.org/10.1016/j.chemosphere.2011.03.061 Polycyclic aromatic hydrocarbons are very stable compounds and tend to bioaccumulate in the environment due to their high degree of conjugation and aromaticity. Hydrous pyrolysis is explored as a technique for the treatment of industrial water containing PAH, using anthracene as a model compound. The reactivity of anthracene under a range of temperatures and durations are studied in this paper. Aliquots of 1.0-10.0mg of anthracene in a range of 1.0-5.0 mL of H(2)O are subjected to hydrous pyrolysis under varied conditions of tempera…

Environmental EngineeringEnvironmental remediationHealth Toxicology and MutagenesisIndustrial WasteIncinerationIndustrial waterWaste Disposal FluidIndustrial wastechemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryHydrous pyrolysisAnthracenesAnthraceneWaste managementVDP::Mathematics and natural science: 400::Chemistry: 440Public Health Environmental and Occupational HealthOxidation reductionGeneral MedicineGeneral ChemistryHydrogen PeroxideSilicon DioxidePollutionFluorocarbon PolymerschemistryPyrolysisWater Pollutants Chemical
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Strong influence of the exposure medium on mutagenicity in the Ames test: 7-methylbenz[a]anthracene-5,6-oxide.

1991

We have previously shown that the activity of the ionized mutagen, 1-hydroxmethylpyrene sulphate, is strongly enhanced in Salmonella typhimurium TA98, when KCl is present in the exposure medium (50-fold at a concentration of 125 mM KCl) and that the halogen ion is responsible for this effect. Here we show that KCl has the opposite effect on the activity of the lipophilic mutagen, 7-methylbenz[a]anthracene-5,6-oxide, (10-fold decrease at a concentration of 125 mM) and that K+ accounts for this influence. Many other solutes also decreased the mutagenicity of 7-methylbenz[a]anthracene-5,6-oxide, but to a smaller extent than the K+ salts. The stability of 7-methylbenz[a]anthracene-5,6-oxide did…

Salmonella typhimuriumHealth Toxicology and MutagenesisEpoxideMutagenToxicologymedicine.disease_causeAmes testPotassium ChlorideToxicologychemistry.chemical_compoundGeneticsmedicineBenz(a)AnthracenesGenetics (clinical)AnthracenebiologyStrain (chemistry)Mutagenicity TestsWaterbiology.organism_classificationEnterobacteriaceaeCulture MediaDistilled waterchemistryBacteriaNuclear chemistryMutagensMutagenesis
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Confined growth of carbon nanoforms in one-dimension by fusion of anthracene rings inside the pores of MCM-41

2014

We report a simple two-step procedure that uses anthracene, a cheap polyaromatic hydrocarbon with low melting point, as a molecular precursor to produce carbon nanoforms (CNFs). First, we describe the chemical synthesis of graphite from the fusion of anthracene rings at relatively low temperature (520 °C) followed by cyclodehydrogenation. Next, we extend this protocol to the synthesis of CNFs by confining the molecular precursor in a mesoporous host like MCM-41. The confined environment favors one-dimensional growth of CNFs with sizes controlled by the pores of the mesoporous host.

FusionAnthraceneMaterials scienceLow melting pointchemistry.chemical_elementNanotechnologyChemical synthesischemistry.chemical_compoundChemical engineeringchemistryMCM-41General Materials ScienceGraphiteMesoporous materialCarbonNanoscale
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Supramolecular interactions of hexacyanocobaltate(III) with polyamine receptors containing a terminal anthracene sensor

2003

Abstract The fluorescence emission properties of a series of chemosensors containing a polyamine receptor bearing an anthracene signaling unit were studied. The fluorescence emission intensity is dependent on the protonation degree of the receptor, the fully protonated form exhibiting the highest emission intensity. By removing protons from the nitrogens a quenching effect can be observed, due to an electron-transfer from the amine to the excited fluorophore. The rate constant of the quenching process is exponentially dependent on the distance of the nitrogen from which the electron is transferred (β=0.6 A−1). The ability of the chemosensors for signaling anions was tested through the model…

AnthraceneFluorophoreGeneral Chemical EngineeringSupramolecular chemistrySolvationGeneral Physics and AstronomyProtonationGeneral ChemistryPhotochemistryFluorescencechemistry.chemical_compoundReaction rate constantchemistryExcited statePhysics::Chemical PhysicsJournal of Photochemistry and Photobiology A: Chemistry
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