Search results for "quinones"

showing 10 items of 114 documents

Polydimethylsiloxane composites containing 1,2-naphtoquinone 4-sulphonate as unique dispositive for estimation of casein in effluents from dairy indu…

2015

A unique dispositive to determine casein which is the most abundant protein in dairy sewages has been proposed. In this sensing technology, the derivatization reagent 1,2-naphtoquininone 4-sulphonate (NQS) is embedded into a polydimethylsiloxane-tetraethylortosilicate-SiO2 nanoparticles composite (PDMS-TEOS-SiO2NPs). When the composite is immersed into the samples, casein is extracted from the solution and derivatized inside the PDMS matrix after 10 min at 100°C. The sensing support changes its color from yellow to orange depending on the casein concentration. Quantitative analysis can be carried out by measuring the absorbance with a reflection probe or by image-processing tool (GIMP). Thi…

Composite numberNQSNanoparticleWastewaterBiochemistryAnalytical ChemistryAbsorbancechemistry.chemical_compoundCaseinEnvironmental ChemistryAnimalsDimethylpolysiloxanesDerivatizationSpectroscopyChromatographyPolydimethylsiloxaneCaseinsSilicon DioxideDairyingchemistryReagentColorimetryIndicators and ReagentsSpectrophotometry UltravioletSulfonic AcidsNaphthoquinonesAnalytica chimica acta
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Pseudomonas litolaris sp. nov., isolated from mediterranean seawater

2012

Strains 2SM5T and 2SM6, two strictly aerobic chemo-organotrophic gammaproteobacteria, were isolated from Mediterranean seawater off the coast of Vinaroz, Castellón, Spain, in February, 1990. They were extensively characterized by a polyphasic study that placed them in the genus Pseudomonas. Phylogenetic analysis of 16S rRNA gene sequences showed that both strains shared 100 % sequence similarity and were closely related to members of the Pseudomonas pertucinogena clade, with less than 97.3 % similarity to strains of established species; Pseudomonas xiamenensis was the closest relative. Analysis of sequences of three housekeeping genes, rpoB, rpoD and gyrB, further confirmed the phylogenetic…

DNA BacterialGenotypeMolecular Sequence DataBiologyDNA RibosomalMicrobiologyPseudomonas pertucinogenaBacterial ProteinsSpecies SpecificityPseudomonasRNA Ribosomal 16SGammaproteobacteriaBotanySeawaterCladePhylogenyEcology Evolution Behavior and SystematicsBase CompositionPhylogenetic treeMediterranean RegionFatty AcidsPseudomonasQuinonesGenes rRNASequence Analysis DNAGeneral MedicinerpoB16S ribosomal RNAbiology.organism_classificationLipidsBacterial Typing TechniquesHousekeeping genePhenotypeSpain
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Sphingobium aromaticiconvertens sp. nov., a xenobiotic-compound-degrading bacterium from polluted river sediment.

2007

A bacterial strain capable of degrading some monochlorinated dibenzofurans, designated RW16T, was isolated from aerobic River Elbe sediments. The strain was characterized based on 16S rRNA gene sequence analysis, DNA G+C content, physiological characteristics, polyamines, ubiquinone and polar lipid pattern and fatty acid composition. This analysis revealed that strain RW16T represents a novel species of the genus Sphingobium. The DNA G+C content of strain RW16T, 60.7 mol%, is the lowest yet reported for the genus. 16S rRNA gene sequence analysis placed strain RW16T as an outlier in the genus Sphingobium. The name Sphingobium aromaticiconvertens sp. nov. is proposed for this dibenzofuran-min…

DNA BacterialGeologic SedimentsMolecular Sequence DataMicrobiologyDNA RibosomalMicrobiologychemistry.chemical_compoundRiversGermanyRNA Ribosomal 16SSequence Homology Nucleic AcidSphingobium aromaticiconvertensPolyaminesWater Pollution ChemicalEcology Evolution Behavior and SystematicsPhospholipidsPhylogenyBenzofuransBase CompositionRiver sedimentbiologyEcologyFatty AcidsQuinonesGenes rRNAGeneral MedicineSequence Analysis DNABiodegradationDibenzofurans Polychlorinated16S ribosomal RNAbiology.organism_classificationBacterial Typing TechniquesSphingomonadaceaeRNA BacterialchemistryCarbohydrate MetabolismXenobioticGenus SphingobiumDNABacteriaInternational journal of systematic and evolutionary microbiology
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Actibacterium mucosum gen. nov., sp. nov., a marine alphaproteobacterium from Mediterranean seawater

2012

Strain R46T, a marine alphaproteobacterium, was isolated from Mediterranean seawater at Malvarrosa beach, Valencia, Spain. It is an aerobic chemo-organotrophic, mesophilic and slightly halophilic organism, with complex ionic requirements. Phylogenetic analyses based on the 16S rRNA and gyrB gene sequences showed that strain R46T formed a separate branch within the family Rhodobacteraceae , bearing similarities below 94.7 and 80.3 %, respectively, to any other recognized species. It contained Q10 as the predominant isoprenoid quinone and C18 : 1ω7c/C18 : 1ω6c as the major cellular fatty acid. Phosphatidylglycerol was the only identified polar lipid, although other lipids were also detected. …

DNA BacterialMolecular Sequence DataBiologyMicrobiologyGenusPhylogeneticsRNA Ribosomal 16SBotanyMediterranean SeaSeawaterRhodobacteraceaePhylogenyEcology Evolution Behavior and SystematicsBase CompositionPhylogenetic treeStrain (chemistry)Fatty AcidsQuinonesPhosphatidylglycerolsSequence Analysis DNAGeneral MedicineRibosomal RNA16S ribosomal RNAHalophileBacterial Typing TechniquesType speciesSpainInternational Journal of Systematic and Evolutionary Microbiology
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Isolation and identification of new anthraquinones from Rhamnus alaternus L and evaluation of their free radical scavenging activity

2018

From the butanolic and the ethyl acetate extracts of Rhamnus alaternus L root bark and leaves, three new anthraquinone glycosides, alaternosides A-C (1,4,6,8 tetrahydroxy-3 methyl anthraquinone 1-O-ß-D-glucopyranosyl-4,6-di-O-α-L-rhamnopyranoside (1); 1,2,6,8 tetrahydroxy-3 methyl anthraquinone 8-O-ß-D-glucopyranoside (2) and 1, 6 dihydroxy-3 methyl 6 [2′-Me (heptoxy)] anthraquinone (3)) were isolated and elucidated together with the two known anthraquinone glycosides, Physcion-8-O-rutinoside (4) and emodin-6-O-α-L-rhamnoside (5) as well as with the known kaempferol-7-methylether (6), β-sitosterol (7) and β-sitosterol-3-O-glycoside (8). Their chemical structures were elucidated using spectr…

DPPHRadicalEthyl acetateAnthraquinonesPlant Science01 natural sciencesBiochemistryAnthraquinoneMedicinal chemistryAnalytical Chemistrychemistry.chemical_compoundRhamnus alaternusAnthraquinonesGlycosidesKaempferolschemistry.chemical_classificationbiologyMolecular Structure010405 organic chemistryPlant ExtractsOrganic ChemistryGlycosideFree Radical Scavengersbiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistryRhamnuschemistryvisual_artvisual_art.visual_art_mediumBark
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Amphetamine and methamphetamine determination in urine by reversed-phase high-performance liquid chromatography with sodium 1,2-napthoquinone 4-sulfo…

1995

A rapid method is described for the identification and determination of amphetamine and methamphetamine in human urine samples by liquid chromatography with UV-Vis detection. The samples were transferred onto a C18 solid-phase extraction column and chromatographed on a Hypersil ODS RP C18, 5 microns (250 x 4 mm I.D.) with an acetonitrile-water elution gradient containing propylamine. Under these conditions, the amines are eluted with a short retention time. The procedure has been applied to the determination of amphetamine and methamphetamine in the range 0.3-4.0 micrograms/ml in spiked urine samples. The detection limits at 280 nm were 4 and 2 ng/ml for amphetamine and methamphetamine, res…

Detection limitChromatographySpectrophotometry InfraredElutionChemistryExtraction (chemistry)Reproducibility of ResultsPropylamineGeneral ChemistryMethamphetamineHigh-performance liquid chromatographyMethamphetamineAmphetaminechemistry.chemical_compoundmedicineHumansIndicators and ReagentsSolid phase extractionQuantitative analysis (chemistry)Chromatography High Pressure LiquidNaphthoquinonesmedicine.drugJournal of Chromatography B: Biomedical Sciences and Applications
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Electronic fluxes during diels-alder reactions involving 1,2-benzoquinones: mechanistic insights from the analysis of electron localization function …

2012

By means of the joint use of electron localization function (ELF) and Thom's catastrophe theory, a theoretical analysis of the energy profile for the hetero-Diels-Alder reaction of 4-methoxy-1,2-benzoquinone 1 and methoxyethylene 2 has been carried out. The 12 different structural stability domains obtained by the bonding evolution theory have been identified as well as the bifurcation catastrophes (fold and cusp) responsible for the changes in the topology of the system. This analysis permits finding a relationship between the ELF topology and the evolution of the bond breaking/forming processes and electron pair rearrangements through the reaction progress in terms of the different ways o…

Diels-Alder reactionsElectron pairElectron localization functionMolecular StructureChemistryCatastrophe theoryRegioselectivityElectronsGeneral ChemistryElectron localization function12-benzoquinonesComputational MathematicsRegioselectivityEnergy profileNucleophileChemical physicsComputational chemistryElectrophileBenzoquinonesQuantum TheoryDensity functional theoryCatastrophe theoryJournal of Computational Chemistry
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A method for the determination of dimethylamine in air by collection on solid support sorbent with subsequent derivatization and spectrophotometric a…

2005

A new method for dimethylamine determination in air is reported. The proposed assay is based on the employment of C18-packed solid phase extraction cartridges for sampling. The retained amine is then derivatized inside the cartridges with the reagent 1,2-naphthoquinone-4-sulfonate. By observing the coloured area of the cartridge, a semiquantitative estimation of the amine can be made. It was also possible to distinguish between primary and secondary amines by visual inspection. Quantitative tests entailed desorption from the cartridges of the derivatives formed, and measurement of the absorbance of the collected extracts. The selected conditions were applied to quantify dimethylamine up to …

DiethylamineDetection limitChromatographyAirOrganic ChemistryReproducibility of ResultsGeneral MedicineBiochemistrySensitivity and SpecificityAnalytical ChemistryCartridgechemistry.chemical_compoundchemistrySpectrophotometryReagentSample preparationSolid phase extractionVolatilizationDerivatizationDimethylamineDimethylaminesNaphthoquinonesJournal of chromatography. A
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Slow Relaxation of the Magnetization in Anilato-Based Dy(III) 2D Lattices.

2021

The search for two- and three-dimensional materials with slow relaxation of the magnetization (single-ion magnets, SIM and single-molecule magnets, SMM) has become a very active area in recent years. Here we show how it is possible to prepare two-dimensional SIMs by combining Dy(III) with two different anilato-type ligands (dianions of the 3,6-disubstituted-2,5-dihydroxy-1,4-benzoquinone: C6O4X22−, with X = H and Cl) in dimethyl sulfoxide (dmso). The two compounds prepared, formulated as: [Dy2(C6O4H2)3(dmso)2(H2O)2]·2dmso·18H2O (1) and [Dy2(C6O4Cl2)3(dmso)4]·2dmso·2H2O (2) show distorted hexagonal honeycomb layers with the solvent molecules (dmso and H2O) located in the interlayer space and…

Dy(III)Models Molecularhoneycomb structureMaterials sciencePharmaceutical ScienceCrystal structureArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundMagnetizationFI-SIMlcsh:Organic chemistryCoordination ComplexesDrug DiscoveryBenzoquinonesDysprosiumMoleculePhysical and Theoretical ChemistryMolecular StructureDimethyl sulfoxideOrganic ChemistryRelaxation (NMR)SIMSMMSolventCrystallographychemistrylayered materialsChemistry (miscellaneous)MagnetMolecular MedicineDerivative (chemistry)anilato ligandsMolecules (Basel, Switzerland)
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Biomimetic oxidation of pyrene and related aromatic hydrocarbons. Unexpected electron accepting abilities of pyrenequinones

2014

We present a mild catalytic method to oxidize PAHs and, in particular, pyrene. The pyrenediones are much better electron acceptors than benzoquinone in the gas phase and present similar accepting abilities in solution.

ElectronsElectronPhotochemistryHydrocarbons AromaticCatalysisGas phaseCatalysischemistry.chemical_compoundBiomimeticsMaterials ChemistryOrganic chemistryElectrodeschemistry.chemical_classificationPyrenesMetals and AlloysQuinonesOxidation reductionGeneral ChemistryElectron acceptorBenzoquinoneSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesPyreneOxidation-ReductionCatalytic method
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