Search results for "YRE"

showing 10 items of 1025 documents

Kinetics of styrene biodegradation by Pseudomonas sp. E-93486

2011

The research into kinetics of styrene biodegradation by bacterial strain Pseudomonas sp. E-93486 coming from VTT Culture Collection (Finland) was presented in this work. Microbial growth tests in the presence of styrene as the sole carbon and energy source were performed both in batch and continuous cultures. Batch experiments were conducted for initial concentration of styrene in the liquid phase changed in the range of 5–90 g m−3. The Haldane model was found to be the best to fit the kinetic data, and the estimated constants of the equation were: μm = 0.1188 h−1, KS = 5.984 mg l−1, and Ki = 156.6 mg l−1. The yield coefficient mean value \documentclass[12pt]{minimal} \usepackage{amsmath} \…

ChemistryBatch experimentKineticsAnalytical chemistryGeneral MedicineChemostatBacterial growthApplied Microbiology and BiotechnologyBiotechnological Products and Process EngineeringCarbonDilutionStyreneKineticschemistry.chemical_compoundChemostatPseudomonasYield (chemistry)Organic chemistrySensitivity (control systems)Energy sourceStyreneBiotransformationBiotechnologyApplied Microbiology and Biotechnology
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Alkyloxy modified pyrene fluorophores with tunable photophysical and crystalline properties

2019

Novel alkyloxy modified 2,7-di-tert-butyl-4,5,9,10-tetra(arylethynyl)pyrenes were prepared through a straightforward Sonogashira coupling approach. Optical properties such as quantum yields and absorption/emission spectra of the fluorophores were investigated by UV/Vis and fluorescence measurements. Aggregation induced excimer formation of the chromophores in polar solvents and in the solid state was proved by the presence of a characteristic bathochromically shifted emission band and a decrease of the emission capability. These results strongly indicate the unexpected observation that the excimer formation of adjacent pyrene rings is not prevented by the introduction of bulky tert-butyl su…

ChemistryChemieSonogashira coupling02 engineering and technologyGeneral ChemistryChromophore010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryExcimer01 natural sciencesFluorescenceCatalysis0104 chemical sciencesLiquid crystals Luminophore pyrene crystal packingchemistry.chemical_compoundMaterials ChemistryMoleculePyreneEmission spectrumSettore CHIM/07 - Fondamenti Chimici Delle TecnologieAbsorption (chemistry)0210 nano-technology
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Size Dependence of Tracer Diffusion in Supercooled Liquids

1996

We have determined by forced Rayleigh scattering the diffusion coefficients D of several photochromic tracers with van der Waals radii between 0.38 and 8 nm (the largest ones being photolabeled polystyrene micronetworks) in 10 glass-forming liquids at temperatures between the glass temperature Tg and ∼1.2Tg. The results were analyzed in terms of power law plots, D(T) ∝ T/η(T)ξ, where η is the solvent shear viscosity, and temperature shifts, D(T) ∝ T/η(T + ΔT). The shift ΔT was related with the width of the rotational correlation time distribution via the time−temperature superposition principle.

ChemistryDiffusionGeneral EngineeringThermodynamicsPower lawPhysics::Fluid DynamicsCondensed Matter::Soft Condensed Mattersymbols.namesakeSuperposition principlechemistry.chemical_compoundsymbolsVan der Waals radiusPolystyrenePhysical and Theoretical ChemistrySupercoolingGlass transitionRotational correlation timeThe Journal of Physical Chemistry
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A theoretical study of the electronic spectrum of styrene

1999

Abstract The electronic spectrum of styrene has been studied by using multiconfigurational second-order perturbation theory (CASPT2). The study includes geometry optimization of the ground state, the lowest triplet state, and the lowest singlet excited state. The covalent 2 1 A ′ state placed vertically at 4.34 eV is assigned to the first band. The 1 1 A ′→3 1 A ′ transition located at 4.97 eV is responsible for the second band. The most intense feature involves the 5 1 A ′ state, which is calculated to lie 6.19 eV above the ground state. The lowest singlet–singlet Rydberg transition (3s) is predicted to occur at 5.85 eV.

ChemistryGeneral Physics and AstronomyEnergy minimizationStyrenesymbols.namesakechemistry.chemical_compoundComputer Science::Systems and ControlExcited stateRydberg formulasymbolsSinglet statePhysical and Theoretical ChemistryPerturbation theoryTriplet stateAtomic physicsGround stateChemical Physics Letters
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Mono- and Tripodal Porphyrins: Investigation on the Influence of the Number of Pyrene Anchors in Carbon Nanotube and Graphene Hybrids.

2020

A series of molecular precursors, containing one (1 and 3) or three (2 and 4) pyrene anchors, covalently linked to porphyrins (free base or Zn), were prepared and characterized. All of them enable ...

ChemistryGrapheneFree baseGeneral ChemistryCarbon nanotubeBiochemistryCatalysislaw.inventionchemistry.chemical_compoundColloid and Surface ChemistryCovalent bondlawPolymer chemistryPyreneJournal of the American Chemical Society
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Ancillary Ligand Effect on Single-Site Styrene Polymerization:  Isospecificity of Group 4 Metal Bis(phenolate) Catalysts

2003

Styrene is polymerized isospecifically by group 4 metal complexes that contain a C2-symmetrically coordinated 1,4-dithiabutane-linked bis(phenolato) ligand activated by methylaluminoxane.

ChemistryLigandMethylaluminoxaneGeneral ChemistryBiochemistryCatalysisStyreneCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryPolymerizationSingle siteGroup (periodic table)visual_artPolymer chemistryvisual_art.visual_art_mediumJournal of the American Chemical Society
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Radioactively labelled epoxides. Part VI. tritium-labelled mono- and dimethyl substituted phenyl oxiranes (styrene oxides)

1988

Tritium-labelled (E)- and (Z)-2,3-dimethyl-2-phenyl oxirane 4, (E)- and (Z)-2-methyl-3-phenyl oxirane 7 and 2,2-dimethyl-3-phenyl oxirane 11 have been prepared by reduction of the corresponding bromoketones with sodium borotritide to the corresponding bromohydrins followed by cyclization to the oxiranes. These oxiranes were successfully used as diagnostic substrates to distinguish between different forms of epoxide hydrolase and glutathione transferase.

ChemistryOrganic ChemistryBiochemistryAnalytical ChemistryStyreneGlutathione transferasechemistry.chemical_compoundDrug DiscoveryOrganic chemistryRadiology Nuclear Medicine and imagingTritiumEpoxide hydrolaseSpectroscopySodium borotritideJournal of Labelled Compounds and Radiopharmaceuticals
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Stamping of monomeric SAMs as a route to structured crystallization templates: patterned titania films.

2000

Gold-coated glass slides have be patterned by using self-assembled monolayers (SAM) of alkane thiols. Through the use of a special thiol terminated with a styrene monomer, microstructures of 5 to 10 microm width and 70 A height have been formed on the surface by graft polymerization of styrene. These patterned gold slides have then been used to template the precipitation of thin titania films from ethanolic solutions of titanium isopropoxide to create microstructured architectures in the film. Plasmon resonance spectra have established the presence of different steps in the process and have been used to follow the kinetics of the precipitation of titania on the surface. The structured TiO2 …

ChemistryOrganic ChemistryNanotechnologyGeneral ChemistryCatalysisStyrenelaw.inventionchemistry.chemical_compoundMonomerPolymerizationChemical engineeringlawMonolayerSelf-assemblyTitanium isopropoxideSurface plasmon resonanceCrystallizationChemistry (Weinheim an der Bergstrasse, Germany)
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1H,13C and17O NMR study of aromatic ring-substituted monochloro- and monobromo-(E)-3-phenylpropenals

1991

Trans-Cinnamaldehydes (CAs) or o-, m- and p-X-(E)-3-phenylpropenals; (X = Cl or Br) were synthesized and their 1H, 13C and 17O NMR spectra were measured, assigned and analysed. The long-range benzylic couplings are discussed in terms of the conformational characteristics of the related styrene systems. The 1H, 13C and 17O NMR substituent chemical shifts of the CA derivatives were compared with those of styrene and explained by the π-electron delocalization in the conjugated CCCO bond system of CA.

ChemistryStereochemistryChemical shiftSubstituentGeneral ChemistryNuclear magnetic resonance spectroscopyConjugated systemRing (chemistry)Medicinal chemistryStyrenechemistry.chemical_compoundDelocalized electronGeneral Materials ScienceSolvent effectsMagnetic Resonance in Chemistry
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Phase-distribution chromatography (PDC) of polystyrene

1970

A chromatographic technique is described where the stationary phase is a layer of a very high molecular polystyrene fraction (M = 107) on glass beads (ballotines). The mobile phase is cyclohexane passing the column at a constant temperature below the theta-temperature. A polystyrene sample of sufficiently low molecular weight (M ≤ 106) injected as a small plug at the top of the column is fractionated because the distribution between the mobile and the stationary phase depends on the molecular weight. Since the large molecules preferentially remain in the stationary phase, the smaller molecules leave the column first. The fractionation effect is inverse to that found in GPC experiments. The …

Chiral column chromatographychemistry.chemical_compoundChromatographyColumn chromatographychemistryCyclohexanePhase (matter)Analytical chemistryMoleculeFraction (chemistry)PolystyreneFractionationJournal of Polymer Science Part A-2: Polymer Physics
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