Search results for "quench"

showing 10 items of 306 documents

Photooxidations of Alkenes in Fluorinated Constrained Media:  Fluoro-organically Modified NaY as Improved Reactors for Singlet Oxygen “Ene” Reactions

2007

Creating a stationary fluorinated environment inside the zeolite cavity can increase the reactivity observed for intrazeolite photooxidation of alkenes. Exchanging the zeolite with fluorinated organic cations is a much more effective strategy than simply using a fluorinated solvent for slurry irradiations. Use of cations containing C-F bonds is also more efficient than use of deuterated cations for creation of a singlet oxygen friendly environment where the quenching processes are slowed down. Doping the zeolite with fluoro-organic cation 4 resulted in an increase in the singlet oxygen lifetime to 12 micros.

chemistry.chemical_classificationQuenching (fluorescence)ZEOLITESChemistryAlkeneSinglet oxygenOrganic ChemistryInorganic chemistryINTRAZEOLITE PHOTOOXIDATIONSLIFETIMEOXIDATIONPhotochemistrySolventchemistry.chemical_compoundCHEMISTRYReactivity (chemistry)Singlet stateDEACTIVATIONOLEFINSZeoliteEne reactionThe Journal of Organic Chemistry
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New insights into the water-solubilization of thiol-sensitive fluorogenic probes based on long-wavelength 7-hydroxycoumarin scaffolds

2014

Abstract The synthesis and photophysical properties of novel water-soluble phenol-based fluorophores derived from 3-benzothiazolyl-7-hydroxycoumarin and emitting in the range 485–631 nm are described. Further conversion into thiol-sensitive fluorogenic probes through the chemical modification of their hydroxyl group was next investigated. Depending on the type of thiol-reactive quenching moiety used (2,4-dinitrobenzenesulfonyl ester, 2,4-dinitrophenyl ether or benzoquinone-type Michael acceptors) and the water-solubilizing group(s) pre-introduced into the coumarin core, dramatic differences in the thiol-induced fluorescence activation of these pro-fluorophores under physiological conditions…

chemistry.chemical_classificationQuenching (fluorescence)[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringChemical modificationEther[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.THER]Chemical Sciences/Medicinal ChemistryPhotochemistryCoumarinFluorescence[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiolPhenolMoietyComputingMilieux_MISCELLANEOUS[CHIM.CHEM]Chemical Sciences/CheminformaticsDyes and Pigments
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Hydrodynamic mechanisms of spinodal decomposition in confined colloid-polymer mixtures: A multiparticle collision dynamics study

2013

A multiscale model for a colloid-polymer mixture is developed. The colloids are described as point particles interacting with each other and with the polymers with strongly repulsive potentials, while polymers interact with each other with a softer potential. The fluid in the suspension is taken into account by the multiparticle collision dynamics method (MPC). Considering a slit geometry where the suspension is confined between parallel repulsive walls, different possibilities for the hydrodynamic boundary conditions (b.c.) at the walls (slip versus stick) are treated. Quenching experiments are considered, where the system volume is suddenly reduced (keeping the density of the solvent flui…

chemistry.chemical_classificationQuenchingPolymersSpinodal decompositiondigestive oral and skin physiologyTime evolutionGeneral Physics and AstronomySlip (materials science)PolymerMolecular Dynamics Simulationbody regionsCondensed Matter::Soft Condensed MatterColloidClassical mechanicschemistryChemical physicsddc:540HydrodynamicsColloidsBoundary value problemPhysical and Theoretical ChemistrySolubilityThe Journal of Chemical Physics
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Spinodal demixing, percolation and gelation of biostructural polymers

1990

We present a variety of new experiments which concern the self-assembly of a polymeric network from homogeneous solutions of Agarose, a representative biostructural polysaccharide used for previous studies at our laboratories. They allow deriving a semi-quantitative phase diagram in the T, C plane. The diagram includes both the spinodal and gelation lines. Below a value of about 2% w/v, concentration is not sufficient for direct gelation; however, quenching of the sol from high temperatures to below the spinodal line initiates the spinodal demixing. The latter generates two sets of regions having respectively, higher- and lower-than-average polymer concentrations. In the higher-concentratio…

chemistry.chemical_classificationQuenchingSpinodalMaterials sciencePolymers and PlasticsPlane (geometry)Organic ChemistryDiagramKineticsPolymerCondensed Matter PhysicsCrystallographychemistryChemical physicsPercolationMaterials ChemistryPhase diagramMakromolekulare Chemie. Macromolecular Symposia
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Time-Resolved study of network self-organization from a biopolymeric solution

1991

Time-resolved studies of network self-organization from homogeneous solutions of the representative biostructural polymer agarose are presented. Solutions are temperature quenched and observed by several techniques. Consistent with previous suggestions by the authors, experiments at concentrations up to about 1.75% w/v provide direct kinetic evidence for the occurrence of at least two distinct processes, leading, in sequence, to self-assembly. These are as follows: (a) a liquid–liquid phase separation of the solution occurring via spinodal demixing and resulting in two sets of regions that have, respectively, higher and lower than average concentrations of random-coiled polymers; and (b) th…

chemistry.chemical_classificationQuenchingSpinodalOrganic ChemistryBiophysicsGeneral MedicinePolymerBranching (polymer chemistry)BiochemistryInstabilityBiomaterialschemistry.chemical_compoundchemistryChemical physicsHelixOrganic chemistryAgarosePhase diagramBiopolymers
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Unexpectedly ambivalent O-2 role in the autocatalytic photooxidation of 2-methoxybenzyl alcohol in water

2015

An unusual autocatalytic photooxidation of 2-methoxybenzyl alcohol has been observed under UV irradiation in aqueous medium. The homogeneous oxidation is catalyzed by the corresponding aldehyde that is also the main oxidation product. The trend of alcohol disappearance rate matches the typical shape of an autocatalytic process, where a crucial and ambivalent role is played by the presence of molecular oxygen. Low oxygen concentrations give rise to a zero-order reaction since the beginning of irradiation, while higher amounts of oxygen reduce the alcohol oxidation rate until the aldehyde reaches a concentration high enough to speed up the alcohol's conversion. Experiments performed by varyin…

chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionAutocatalytic photooxidation 2-Methoxybenzyl alcohol 2-Methoxybenzaldehyd O2 quenchingHomogeneous photocatalysisProcess Chemistry and Technologychemistry.chemical_elementAlcoholSettore CHIM/06 - Chimica OrganicaPhotochemistryOxygenAldehydeCatalysisCatalysisAutocatalysischemistry.chemical_compoundchemistrySettore CHIM/03 - Chimica Generale E InorganicaAlcohol oxidationPhysical and Theoretical ChemistryAbsorption (chemistry)
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Multiple interactions between molecular and supramolecular ordering

1999

We report studies of the interplay among processes of molecular conformational changes, spinodal demixing of the solution, and molecular crosslinking involved in the physical gelation of a biopolysaccharide-water system. Multiple interactions and kinetic competition among these processes were studied under largely different absolute and relative values of their individual rates by appropriate choices of the quenching temperature at constant polymer concentration. Quenching temperature strongly affects the rate of growth but not the final value of the fractal dimension of the gel. Kinetic competition plays a central role in determining the final conformation of individual molecules and the s…

chemistry.chemical_classificationSpinodalQuenching (fluorescence)chemistryChemical physicsKineticsCondensationSupramolecular chemistryMoleculePhysical chemistryPolymerFractal dimensionPhysical Review E
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Effective conjugation in conjugated polymers with strongly twisted backbones: A case study on fluorinated MEHPPV

2016

Conjugated polymers with strongly twisted backbones, such as MEHPPV with fluorinated vinylene units (F-MEHPPV), demand a redefinition of the all-important ‘effective conjugation length’ ECL, which we extract here by a facile graphical method. In MEHPPV (being essentially planar), the ECL coincides with the ‘maximum conducive chain length’ MCC and extends over about n ≈ 9 repetition units (RU). In F-MEHPPV, the MCC is similarly long with n ≈ 8, but the ECL localizes on just one RU. The strong twist in F-MEHPPV persists in the excited state, broadening the emission spectrum and quenching the fluorescence with reduced radiative and enhanced non-radiative rates.

chemistry.chemical_classificationfluorinated MEHPPVMaterials scienceQuenching (fluorescence)twisted backbones02 engineering and technologyGeneral ChemistryPolymerConjugated system010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescence0104 chemical sciencesChain lengthPlanarchemistryExcited stateEffective conjugationMaterials ChemistryEmission spectrum0210 nano-technology
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Reliable and simple analytical methods for determination of citrulline and metabolically related amino acids by liquid chromatography after derivatiz…

2014

We describe the development of a high-performance liquid chromatography (HPLC) method for the determination of citrulline and other amino acids relevant to intestinal diseases. The amino acids were derivatized with 9-fluorenylmethylchloroformate (FMOC-Cl) and their derivatives were separated on two different columns, a core-shell column (Halo C18) and a silica-based monolith (Chromolith Performance RP-18). The derivatization reaction was optimized with respect to pH, buffer concentration and reproducibility. The optimal derivatization conditions were achieved with 0.4 M borate buffer at pH 9.20, a constant ratio of FMOC-Cl/total amino acids (10 : 1) and 75 mM tyramine after 1 min (quenching…

chemistry.chemical_classificationgeographyReproducibilityMonolithic HPLC columnQuenching (fluorescence)Chromatographygeography.geographical_feature_categoryResolution (mass spectrometry)General Chemical EngineeringGeneral EngineeringCiencias QuímicasHigh-performance liquid chromatographyMonolithic ColumnsAnalytical ChemistryAmino acidCore-Shell Columnschemistry.chemical_compoundchemistryCitrullineQuímica AnalíticaMonolithAmino AcidsDerivatizationCIENCIAS NATURALES Y EXACTAS
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Binding and Fluorescent Sensing of Dicarboxylates by a Bis(calix[4]pyrrole)-Substituted BODIPY Dye

2013

A bis(calix[4]pyrrole)-substituted BODIPY ditopic receptor 1 has been synthesised and characterised. The binding and sensing properties of 1 towards several aliphatic and aromatic dicarboxylates have been evaluated by using UV/Vis fluorescence and 1H NMR spectroscopy. The receptor strongly binds linear α,ω-dicarboxylates of appropriate lengths (C9 and C10) by acting as a cleft. For all dicarboxylates, the binding event is detected by a bathochromic shift in the UV/Vis spectra of the receptor and by strong quenching of its fluorescence.

chemistry.chemical_compound1h nmr spectroscopyQuenching (fluorescence)chemistryOrganic ChemistryBathochromic shiftmacromolecular substancesVis spectraPhysical and Theoretical ChemistryBODIPYPhotochemistryFluorescencePyrroleEuropean Journal of Organic Chemistry
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