Search results for "Fluorescence"

showing 10 items of 2463 documents

Epifluorescence microscopy studies of fatty acid monolayers: Domain formation induced by polymeric gegenions

1991

The monolayer behavior of long-chain fatty acids at the air/water interface on a poly(ethyleneimine) containing subphase was investigated. The interaction of the polymeric gegenions in the subphase leads to expanded states and permits the visualization of the aggregation behavior of different long-chain fatty acids via fluorescence microscopy. The monolayer morphologies and their variability were intensively studied by fluorescence microscopy. In addition, the transfer of the complexed fatty acid monolayers to solid substrates has been investigated.

chemistry.chemical_classificationPolymers and PlasticschemistryChemical engineeringOrganic ChemistryMonolayerMaterials ChemistryFluorescence microscopeEthyleneimineFatty acidOrganic chemistryCondensed Matter PhysicsDomain formationMakromolekulare Chemie. Macromolecular Symposia
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Single molecule probing of dynamics in supercooled polymers

2011

6 pages; International audience; Fluorescence experiments with single BODIPY molecules embedded in a poly(methyl acrylate) matrix have been performed at various temperatures in the supercooled regime. By using pulsed excitation, fluorescence lifetime and linear dichroism time trajectories were accessible at the same time. Both observables have been analyzed without data binning. While the linear dichroism solely reflects single particle dynamics, the fluorescence lifetime observable depends on the molecular environment, so that the dynamics from the polymer host surrounding a chromophore contributes to this quantity. We observe that the lifetime correlation decays slightly faster than polar…

chemistry.chemical_classificationPolymersAnalytical chemistryGeneral Physics and Astronomy02 engineering and technologyPolymerChromophoreDichroism010402 general chemistry021001 nanoscience & nanotechnologyPolarization (waves)Linear dichroism01 natural sciencesFluorescence0104 chemical scienceschemistry.chemical_compound[CHIM.POLY]Chemical Sciences/PolymerschemistryChemical physicsMoleculePhysical and Theoretical ChemistryBODIPY0210 nano-technologySingle BODIPY moleculesExcitation
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Fluorogenic Enzyme-Triggered Domino Reactions Producing Quinoxalin-2(1H)-one-based Heterocycles

2020

International audience; A simple and effective biocompatible domino reaction triggered by a model protease and leading to formation of strongly fluorescent quinoxalin-2(1H)-one N-heterocycles is described. Some positive attributes including versatility and ability to provide outstanding fluorescence "OFF-ON" responses were revealed by this work. They open the way for practical applications of this novel type of "covalent-assembly" based fluorescent probes in the fields of sensing and bioimaging. Among the myriad of synthetic transformations and catalysts currently available for concise and efficient synthesis of organic molecules, bioinspired approaches based on the use of enzymes often int…

chemistry.chemical_classificationProtease[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistrymedicine.medical_treatmentOrganic Chemistry010402 general chemistryBiocompatible material01 natural sciencesBiochemistryCombinatorial chemistryFluorescenceDomino0104 chemical sciencesEnzymeCascade reactionmedicinePhysical and Theoretical ChemistryOrganic Letters
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Bistetrazine-Cyanines as Double-Clicking Fluorogenic Two-Point Binder or Crosslinker Probes

2018

Fluorogenic probes can be used to minimize the background fluorescence of unreacted and nonspecifically adsorbed reagents. The preceding years have brought substantial developments in the design and synthesis of bioorthogonally applicable fluorogenic systems mainly based on the quenching effects of azide and tetrazine moieties. The modulation power exerted by these bioorthogonal motifs typically becomes less efficient on more conjugated systems; that is, on probes with redshifted emission wavelength. To reach efficient quenching, that is, fluorogenicity, even in the red range of the spectrum, we present the synthesis, fluorogenic, and conjugation characterization of bistetrazine-cyanine pro…

chemistry.chemical_classificationQuenching (fluorescence)010405 organic chemistryChemistryOrganic ChemistryPeptideGeneral ChemistryConjugated system010402 general chemistry01 natural sciencesFluorescenceCombinatorial chemistryCatalysis0104 chemical sciencesTetrazinechemistry.chemical_compoundCovalent bondAzideBioorthogonal chemistryChemistry - A European Journal
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Chiral synthetic pseudopeptidic derivatives as triplet excited state quenchers

2009

The behavior of 6 pseudopeptidic models, synthesized by connecting different protected amino acids (Trp, Tyr, Phe, and Lys) with various diamino spacers, as quenchers of the triplet excited state of tiaprofenic acid (and its methyl ester), has been investigated. A series of quenching constants have been determined, which depend on the nature of the quencher and on the stereochemistry of the excited drug. A significant degree of stereodifferentiation has been found for the peptidomimetic synthesized with Phe and Tyr linked by a piperazine bridge. The obtained results support the utility of laser flash photolysis (LFP) as a tool to investigate the interactions between photoexcited drugs and s…

chemistry.chemical_classificationQuenching (fluorescence)010405 organic chemistryPeptidomimeticStereochemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryPhotochemistryOrganic ChemistryLaser flash photolysis010402 general chemistry01 natural sciencesBiochemistry3. Good health0104 chemical sciencesAmino acidPiperazinechemistry.chemical_compoundchemistryExcited stateQuenchingDrug DiscoveryTriplet excited stateFlash photolysisBinding site
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Photoinduced electron transfer in molecular organizates at the gas-water interface

1994

Abstract The influence of the molecular geometry is of fundamental importance for a better understanding of the photoinduced electron transfer mechanism. Because of their typical molecular structures, cyclophane rings have proved to be suitable for this purpose as electron acceptor molecules adsorbed under an amphiphile monolayer. We used a pyrene-labelled phospholipid derivative both as molecular anchor for the cyclophane ring and electron donor molecule. The co-spreading technique was used to prepare the complex monolayers. Surface pressure and surface potential measurements have indicated similar monolayer behaviour as with dimyristoylphosphatidic acid as anchor molecule, leading to the …

chemistry.chemical_classificationQuenching (fluorescence)ChemistryMetals and AlloysElectron donorSurfaces and InterfacesElectron acceptorPhotochemistryPhotoinduced electron transferSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferMonolayerMaterials ChemistryPyreneCyclophaneThin Solid Films
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Influence of Several Effectors on the Structure-Activity Relationship of Spleen Phosphodiesterase

1993

The influence of Mg(II) and organic solvents on the structure-activity relationship of spleen phosphodiesterase II was analyzed using UV and fluorescence spectroscopies. An increase in the RNase activity found in the presence of Mg(II) was related to the enzyme-Mg(II) interaction detected by UV spectroscopy. In the fluorescence spectra of phosphodiesterase strong hypochromic and bathochromic effects were observed when RNA was present at a concentration (52 μg ml−1) of the same magnitude as the concentration that inhibits the activity (Ki = 40 μg ml−1). The strong quenching observed in the presence of RNA shows the importance of large dynamic and static quenching of the Trp residues of the e…

chemistry.chemical_classificationQuenching (fluorescence)ChemistryPhosphodiesteraseBiochemistryFluorescenceCatalysisFluorescence spectroscopyUltraviolet visible spectroscopyEnzymeBiochemistryBathochromic shiftBiophysicsDenaturation (biochemistry)General Agricultural and Biological SciencesBiotechnologyBiocatalysis
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Photocatalysis within Hyperbranched Polyethers with a Benzophenone Core

2008

Quenching and product studies have been performed to demonstrate the suitability of hyperbranched polyethers with a tetrafunctionalized benzophenone core as photocatalysts. The triplet photosensitized transformation of an unsaturated diazo compound has been used as the model reaction. The polymer with highest molecular weight led to a similar product distribution even after several catalytic cycles, which evidences its excellent photostability under prolonged irradiation time. We attribute this to the stabilizing effect of the hyperbranched polymer shell.

chemistry.chemical_classificationQuenching (fluorescence)Organic ChemistryEtherPolymerPhotochemistryProduct distributionCatalysischemistry.chemical_compoundchemistryPolymer chemistryBenzophenonePhotocatalysisDiazoThe Journal of Organic Chemistry
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‘Interrupted’ diazotization of 3-aminoindoles and 3-aminopyrroles

2014

Abstract ‘Interrupted’ diazotization of 3-aminoindoles and 3-aminopyrroles, achieved by quenching with cold water immediately after the addition of nitrite, led, in good yields, to stable compounds whose structures were identified to be the diazonium species with nitrate as the counter ion, which show no saline character.

chemistry.chemical_classificationQuenching (fluorescence)Organic ChemistryInorganic chemistryPhotochemistryBiochemistrySettore CHIM/08 - Chimica Farmaceuticachemistry.chemical_compoundchemistryNitrateDrug DiscoveryAmino pyrroles Aminoindoles Diazoindoles Diazo pyrrolesNitriteCounterion
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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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