Search results for "Phosphor"

showing 10 items of 1952 documents

[Ir(C^N)2(N^N)]+ emitters containing a naphthalene unit within a linker between the two cyclometallating ligands

2016

The synthesis of four cyclometallated [Ir(C^N) 2 (N^N)][PF 6 ] compounds in which N^N is a substituted 2,2’- -bipyridine (bpy) ligand and the naphthyl-centred ligand 2,7-bis(2-(2-(4-(pyridin-2-yl)phenoxy)ethoxy) ethoxy)naphthalene provides the two cyclometallating C^N units is reported. The iridium( III ) complexes have been characterized by 1 H and 13 C NMR spectroscopies, mass spectrometry and elemental analysis, and their electrochemical and photophysical properties are described. Comparisons are made with a model [Ir(ppy) 2 (N^N)][PF 6 ] compound (Hppy = 2-phenylpyridine). The complexes containing the naphthyl-unit exhibit similar absorption spectra and excitation at 280 nm leads to an …

Absorption spectroscopyChemistryLigandchemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographyExcited stateDensity functional theorySinglet stateIridium0210 nano-technologyPhosphorescenceHOMO/LUMODalton Transactions
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On the Low-Lying Excited States ofsym-Triazine-Based Herbicides

2005

We report a joint computational and luminescence study on the low-lying excited states of sym-triazines, namely, 1,3,5-triazine (1) and the ubiquitous herbicides atrazine [6-chloro-N2-ethyl-N4-isopropyl-1,3,5-triazine-2,4-diamine (2)] and ametryn [6-methylthio-N2-ethyl-N4-isopropyl-1,3,5-triazine-2,4-diamine (3)]. Geometrical structures, energetics, and transition and state properties of I and 2 were computed at the TD-DFT, CASSCF, and CASPT2 levels of theory. The fluorescence and phosphorescence emission spectra, lifetimes, and fluorescence quantum yields were measured for the three compounds, and from these, the energies of the lowest excited states and their corresponding radiative rates…

Absorption spectroscopyQuantum yieldPhotochemistryMolecular physicsAbsorptionAb initio quantum chemistry methodsOscillometryPressureRadiative transferEmission spectrumPhysical and Theoretical ChemistryMolecular StructureChemistry PhysicalHerbicidesTriazinesChemistryTemperatureHydrogen-Ion ConcentrationModels TheoreticalAtomic and Molecular Physics and OpticsSpectrometry FluorescenceModels ChemicalSpectrophotometryExcited stateAtrazineIndicators and ReagentsPhosphorescenceLuminescenceSoftwareChemPhysChem
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Metabolic shift of polyphosphate-accumulating organisms with different levels of polyphosphate storage

2012

Previous studies have shown that polyphosphate-accumulating organisms (PAOs) are able to behave as glycogen-accumulating organisms (GAOs) under different conditions. In this study we investigated the behavior of a culture enriched with Accumulibacter at different levels of polyphosphate (poly-P) storage. The results of stoichiometric ratios Gly degraded/HAc uptake, PHB synthesized/HAc uptake, PHV synthesized/HAc uptake and P release/HAc uptake confirmed a metabolic shift from PAO metabolism to GAO metabolism: PAOs with high poly-P content used the poly-P to obtain adenosine tri-phosphate (ATP), and glycogen (Gly) to obtain nicotinamide adenine dinucleotide (NADH) and some ATP. In a test whe…

Accumulibacter Type IIWaste component removalUnclassified drugPhysiologyChemical compositionMicrobial metabolismStorageWastewaterNicotinamide adenine dinucleotidePolyhydroxyalkanoic acidchemistry.chemical_compoundBacteriumBioreactorsPolyphosphatesGlycolysisAnaerobiosisBiomassPolyphosphate-accumulating organismsWaste Management and DisposalAccumulibacter Type IGlycogen accumulating organismPriority journalWater Science and TechnologyFluorescence microscopyPolyhydroxyvalerateSewageGlycogenHydrolysisFluorescence in situ hybridizationEcological ModelingPhosphorusHydrogen-Ion ConcentrationBioaccumulationPollutionStoichiometryWaste treatmentPolyphosphate-accumulating organismsBiodegradation EnvironmentalEnhanced biological phosphorus removalBiochemistryGlycogen-accumulating metabolism (GAM)Nicotinamide adenine dinucleotideAccumulibacter type 1Accumulibacter type 2GlycolysisGlycogenMetabolic Networks and PathwaysAccumulibacterAdenosine triphosphateEnvironmental EngineeringBiologyAcetic acidArticleAssociative storagePolyphosphate-accumulating metabolism (PAM)PolyphosphateGlycogen-accumulating organismsGlycogen-accumulating metabolismsTECNOLOGIA DEL MEDIO AMBIENTEPolyphosphate accumulating organismCivil and Structural EngineeringPolyphosphate-accumulating organisms (PAO)BacteriaPolyphosphateMetabolismIn situ measurementGlycogen-accumulating organisms (GAO)Polyphosphate-accumulating metabolismsNonhumanAmidesCarbonMetabolismchemistryPolyphosphate (poly-P)Bacterial metabolismCell cultureVolatilizationWater Research
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Determination of phosphorus by instrumental neutron activation and bremsstrahlung measurement in bone samples

1997

A non destructive method based on the31P(n,γ)32P reaction for the assay of phosphorus in bone samples is described. This method involves a thermal neutron irradiation of 2 minutes in a reactor followed by the measurement of the bremsstrahlung produced by the β− of32P in a Ge-detector surrounded by an anti-Compton shield. Accuracy and precision were tested by analysing the certified NIST 1486 Bone Meal reference material and tri-calcium phosphate (Ca3(PO4)2) samples. The value obtained for the reference material was in good agreement with the certified value and with relative standard deviation of 4.1% the precision was acceptable. The value obtained for Ca3(PO4)2 shows a deviation of −6% fr…

Accuracy and precisionMaterials scienceHealth Toxicology and MutagenesisPhosphorusRadiochemistryPublic Health Environmental and Occupational HealthAnalytical chemistryBremsstrahlungchemistry.chemical_elementPollutionNeutron temperatureBone mealAnalytical ChemistryNuclear Energy and EngineeringchemistryNon destructiveRadiology Nuclear Medicine and imagingIrradiationSpectroscopyNeutron activationJournal of Radioanalytical and Nuclear Chemistry
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Chromo-Fluorogenic Detection of Nerve-Agent Mimics Using Triggered Cyclization Reactions in Push-Pull Dyes

2010

A family of azo and stilbene derivatives (1-9) are synthesized, and their chromo-fluorogenic behavior in the presence of nerve-agent simulants, diethylchlorophosphate (DCP), diisopropylfluorophosphate (DFP), and diethylcyanophosphate (DCNP) in acetonitrile and mixed solution of water/acetonitrile (3:1 v/v) buffered at pH 5.6 with MES, is investigated. The prepared compounds contain 2-(2-N,N-dimethylaminophenyl)ethanol or 2-[(2-N,N-dimethylamino)phenoxy]ethanol reactive groups, which are part of the conjugated pi-system of the dyes and are able to give acylation reactions with phosphonate substrates followed by a rapid intramolecular N-alkylation. The nerve-agent mimic-triggered cyclization …

AcetonitrilesIsoflurophateSilica gelOrganic ChemistryWaterGeneral ChemistryConjugated systemPhotochemistryBiochemistryPhosphonateKineticschemistry.chemical_compoundOrganophosphorus CompoundsReaction rate constantchemistryCyclizationReagentSpectrophotometry UltravioletHypsochromic shiftReactivity (chemistry)Chemical Warfare AgentsGasesAcetonitrileFluorescent DyesNuclear chemistryChemistry - An Asian Journal
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Application of the General Model "Biological Nutrient Removal Model No.1" to upgrade two full-scale WWTPs

2012

In this paper, two practical case studies for upgrading two wastewater treatment plants (WWTPs) using the general model BNRM1 (Biological Nutrient Removal Model No. 1) are presented. In the first case study, the Tarragona WWTP was upgraded by reducing the phosphorus load to the anaerobic digester in order to minimize the precipitation problems. Phosphorus load reduction was accomplished by mixing the primary sludge and the secondary sludge and by elutriating the mixed sludge. In the second case study, the Alcantarilla WWTP, the nutrient removal was enhanced by maintaining a relatively low dissolved oxygen concentration in Stage A to maintain the acidogenic bacteria activity. The VFA produce…

AcidogenesisBiological nutrient removalWATER TREATMENT PLANTSAerobic bacteriachemistry.chemical_elementActivated sludge modelPhosphatesWater PurificationWASTE-WATERBNRM1Environmental ChemistryAnaerobiosisOrganic ChemicalsWaste Management and DisposalTECNOLOGIA DEL MEDIO AMBIENTEWater Science and TechnologyCALIBRATIONSewagePhosphorusEnvironmental engineeringGeneral MedicineModels TheoreticalASM2DAerobiosisACTIVATED-SLUDGE MODELActivated sludge modelsEnhanced biological phosphorus removalWastewaterchemistrySIMULATIONPlant-wide mathematical modellingEnvironmental scienceSewage treatmentWater treatmentSanitary EngineeringWWTP upgrading
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Aequorin-expressing yeast emits light under electric control

2011

In this study, we show the use of direct external electrical stimulation of a jellyfish luminescent calcium-activated protein, aequorin, expressed in a transgenic yeast strain. Yeast cultures were electrically stimulated through two electrodes coupled to a standard power generator. Even low (1.5. V) electric pulses triggered a rapid light peak and serial light pulses were obtained after electric pulses were applied periodically, suggesting that the system is re-enacted after a short refraction time. These results open up a new scenario, in the very interphase between synthetic biology and cybernetics, in which complex cellular behavior might be subjected to electrical control.

Activated proteinsLightScyphozoaAequorinApplied Microbiology and BiotechnologyElectricityHydroxidesCellular behaviorsPriority journalYeast electro-stimulationbiologyPhosphorescencePower generatorsGeneral MedicineElectrostimulationMAQUINAS Y MOTORES TERMICOSElectrodeElectric pulseInterphaseBioluminescenceYeast cultureGenetic EngineeringMATEMATICA APLICADABiotechnologyPotassium CompoundsLight pulse generatorsSaccharomyces cerevisiaeBioengineeringNanotechnologyLight pulseSaccharomyces cerevisiaeElectrical stimulationsYeast strainArticleAequorinBioluminescenceBiologySynthetic biologyBioelectronicsBioelectronicsbiology.organism_classificationElectric controlYeastElectric StimulationYeastFISICA APLICADABiophysicsbiology.proteinProtein expressionJellyfishElectrical controlLuminescenceCell functionTransgenics
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Modelling of the ternary system H3PO4/H2O/TBP

2002

Abstract A thermodynamic model is presented for the extraction of phosphoric acid from water by tri-n-butylphosphate (TBP), from aqueous solutions containing 0–6 mol/kg phosphoric acid. The activity coefficient of phosphoric acid was calculated from experimental data using Pitzer’s equation, and those of the components in the organic phase were calculated by Sergievskii–Danus’s relationship. The proposed model gives a satisfactory description of the distribution of phosphoric acid and water, in the considered concentration range, by taking into account the formation of the following species: TBP, TBP·H2O, H3PO4·TBP and (TBP)2·H3PO4·H2O.

Activity coefficientChromatographyAqueous solutionTernary numeral systemChemistryGeneral Chemical EngineeringInorganic chemistryExtraction (chemistry)General Physics and AstronomyThermodynamic modelchemistry.chemical_compoundPhase (matter)Physical and Theoretical ChemistryPhosphoric acidFluid Phase Equilibria
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Ferrocenylbis(ylene) phosphoranes

1997

The ferrocenylbis(methylene)phosphorane Fc-P(=CTms 2 ) 2 ( 1 ) (Fc = −C 5 H 4 FeC 5 H 5 ) can be synthesized starting from ferrocenyldichlorophosphane FcPCl 2 or ferrocenyldilithiophosphane FcPLl 2 . The X-ray structure of ( 1 ) shows some unusual structural features, which indicate considerable electronic interaction of the ferrocenyl group and the σ 3 λ 5 -phosphorane unit. As a consequence of this interaction, the rotational barrier of the methylene bonds is extraordinary low. Therefore, in contrast to other bis(methylene)phosphoranes, the endo - and exo -Tms groups are indistinguishable on the NMR time scale even at −100°C. The analogous ferrocenylbis(imino)phosphorane Fc-P(=NTms) 2 ( 9…

Addition reactionStereochemistryOrganic Chemistrychemistry.chemical_elementBiochemistryPhosphoraneNitrogenInorganic Chemistrychemistry.chemical_compoundchemistryReagentElectrophileX-ray crystallographyMaterials ChemistryFerrocenyl groupPhysical and Theoretical ChemistryMethyleneJournal of Organometallic Chemistry
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Novel mutations of the MET proto-oncogene in papillary renal carcinomas.

1999

Hereditary papillary renal carcinoma (HPRC) is characterized by multiple, bilateral papillary renal carcinomas. Previously, we demonstrated missense mutations in the tyrosine kinase domain of the MET proto-oncogene in HPRC and a subset of sporadic papillary renal carcinomas. In this study, we screened a large panel of sporadic papillary renal carcinomas and various solid tumors for mutations in the MET proto-oncogene. Summarizing these and previous results, mutations of the MET proto-oncogene were detected in 17/129 sporadic papillary renal carcinomas but not in other solid tumors. We detected five novel missense mutations; three of five mutations were located in the ATP-binding region of t…

AdenomaModels MolecularCancer ResearchProtein ConformationDNA Mutational AnalysisMolecular Sequence DataHereditary Papillary Renal Cell CarcinomaBiologymedicine.disease_causeTransfectionProto-Oncogene MasReceptor tyrosine kinaseMiceAdenosine TriphosphateNeoplastic Syndromes HereditaryProto-OncogenesGeneticsCarcinomamedicineMissense mutationAnimalsHumansPoint MutationAmino Acid SequencePhosphorylationCodonMolecular BiologyKidneyMutationBinding SitesSequence Homology Amino AcidPoint mutation3T3 CellsDNA NeoplasmProto-Oncogene Proteins c-metmedicine.diseaseCarcinoma PapillaryKidney NeoplasmsNeoplasm Proteinsmedicine.anatomical_structureCell Transformation NeoplasticCancer researchbiology.proteinMutagenesis Site-DirectedTyrosine kinaseProtein Processing Post-TranslationalSequence AlignmentOncogene
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