Search results for "Fluorescence"

showing 10 items of 2463 documents

Observation of Very Narrow Linewidths in the Fluorescence Excitation Spectra of Single Conjugated Polymer Chains at 1.2 K

2007

Fluorescence emission and excitation spectra of single poly[2-methoxy-5-(2'-ethyl-hexyloxy)-1,4-phenylene vinylene] polymer molecules embedded in poly(methylmethacrylate) have been recorded at 1.2 K. The ubiquitous spectral diffusion causes large variations in the spectral shape and apparent linewidth in the emission spectra. Nevertheless, we find very narrow (approximately 0.1 cm(-1)) purely electronic zero-phonon lines in the excitation spectra, which are 2 orders of magnitude smaller than previous estimates of the homogeneous linewidth. These results complement the molecular description of the low energy transitions in conjugated polymers.

chemistry.chemical_classificationVinyl CompoundsMaterials sciencePolymersGeneral Physics and AstronomyPolymerConjugated systemMolecular physicsFluorescenceFluorescenceLaser linewidthNuclear magnetic resonanceOrders of magnitude (time)chemistryPolymethyl MethacrylateMoleculeEmission spectrumDiffusion (business)Physical Review Letters
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Biochemical identification and tissue-specific expression patterns of keratins in the zebrafish Danio rerio

1998

We have identified a number of type I and type II keratins in the zebrafish Danio rerio by two-dimensional polyacrylamide gel electrophoresis, complementary keratin blot-binding assay and immunoblotting. These keratins range from 56 kDa to 46 kDa in molecular mass and from pH 6.6 to pH 5.2 in isoelectric point. Type II zebrafish keratins exhibit significantly higher molecular masses (56-52 kDa) compared with the type I keratins (50-48 kDa), but the isoelectric points show no significant difference between the two keratin subclasses (type II: pH 6.0-5.5; type I: pH 6.1-5.2). According to their occurrence in various zebrafish tissues, the identified keratins can be classified into "E" (epider…

chemistry.chemical_classificationanimal structuresHistologyintegumentary systembiologyMolecular massCellular differentiationDanioCell Biologybiology.organism_classificationMolecular biologyPathology and Forensic MedicineIsoelectric pointMicroscopy FluorescenceBiochemistrychemistryGenetic modelKeratinAnimalsKeratinsTissue DistributionPolyacrylamide gel electrophoresisZebrafishCytoskeletonZebrafishCell and Tissue Research
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Fluorescence and color as markers for the Maillard reaction in milk–cereal based infant foods during storage

2007

Abstract Free and total fluorescence compounds and color formation were measured in three different milk–cereal based infant foods stored at 25, 30 and 37 °C for 9 months to evaluate the advanced and final stages of the Maillard reaction. Milk–cereal infant foods containing honey (B) or fruits (C) had fluorescent values higher than sample (A) without them. This difference could be ascribed to the higher monosaccharide (fructose and/or glucose) content of (B) and (C), which could increase susceptibility to the Maillard reaction. However, for color increase (ΔE), no significant differences (p

chemistry.chemical_classificationdigestive oral and skin physiologyFood preservationfood and beveragesFructoseGeneral MedicineFluorescenceAnalytical Chemistrychemistry.chemical_compoundMaillard reactionsymbols.namesakechemistrysymbolsMonosaccharideColor formationFood scienceFood ScienceFood Chemistry
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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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Multispectral fluorescence detection of pigmented cutaneous tumours

2020

We investigated pigmented skin tumour lesions in vivo and ex vivo, including benign and dysplastic nevi, as well as malignant lesions, such as pigmented basal cell carcinoma (BCC) and malignant melanoma (MM) lesions, to obtain a complex view about the feasibility of different excitation sources solely and/or in combination to induce fluorescence signal useful for diagnosis of various low-fluorescent cutaneous neoplasia. A specialized multispectral analysis of the data obtained was applied by using excitation in broad spectral range, covering ultraviolet, visible and near-infrared spectral range, that contribute considerably to: (1) fundamental determination of tumour tissues’ spectral prope…

chemistry.chemical_classificationintegumentary systembiologyChemistryMelanomamedicine.diseaseFluorescenceMolecular biologyMelaninIn vivoKeratinmedicinebiology.proteinBasal cell carcinomaSkin cancerElastinBiophotonics—Riga 2020
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A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush

2011

A new biorelevant polymer brush showing a polybenzofulvene backbone was synthesized by a ‘‘grafting through’’ approach based on click chemistry and spontaneous polymerization reactions. The easy polymerization of the relatively complex monomer (6-MOEG-9-TM-BF3k) suggests the existence of a particularly efficient recognition process capable of pre-organizing the monomer molecules for the spontaneous polymerization. 13C-NMR spectroscopy as well as UV-vis and fluorescence spectroscopy suggested for poly-6-MOEG-9-TM-BF3k the features of a vinyl (1,2) p-stacked polymer. The new polybenzofulvene derivative was found to interact with water at room temperature to give clear water solutions, but TEM…

chemistry.chemical_classificationpolymer brushPolymers and PlasticsOrganic ChemistryBioengineeringPolymerPolymer brushCell morphologyBiochemistryFluorescence spectroscopyNMRchemistry.chemical_compoundMonomerchemistryChemical engineeringPolymerizationPolymer chemistryclick chemistryClick chemistryMacromolecule
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Recognition of Viologen Derivatives in Water by N-Alkyl Ammonium Resorcinarene Chlorides

2017

Three water-soluble N-alkyl ammonium resorcinarene chlorides decorated with terminal hydroxyl groups at the lower rims were synthesized and characterized. The receptors were decorated at the upper rim with either terminal hydroxyl, rigid cyclohexyl, or flexible benzyl groups. The binding affinities of these receptors toward three viologen derivatives, two of which possess an acetylmethyl group attached to one of the pyridine nitrogens, in water were investigated via 1H NMR spectroscopy, fluorescence spectroscopy, and isothermal titration calorimetry (ITC). ITC quantification of the binding process gave association constants of up to 103 M–1. Analyses reveal a spontaneous binding process whi…

chemistry.chemical_classificationta114010405 organic chemistryOrganic ChemistryEnthalpyIsothermal titration calorimetryViologenResorcinarene010402 general chemistry01 natural sciencesviologen derivativesFluorescence spectroscopy0104 chemical scienceschemistry.chemical_compoundN-alkyl ammonium resorcinarene chlorideschemistryPyridinePolymer chemistrymedicineOrganic chemistryAmmoniumta116Alkylmedicine.drugJOURNAL OF ORGANIC CHEMISTRY
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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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Luminescence properties of a cofacial dipalladium porphyrin dimer under argon and in the presence of dioxygen

2001

The preparation and luminescence properties of a dipalladium cofacial porphyrin dimer (DPA) Pd 2 (where DPA is the tetraanion of 1,8-bis(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrin-5-yl)anthracene) are reported and compared together with the photophysical behavior of the known monomeric (OEP)Pd and (TPP)Pd complexes. The effect of dioxygen in the presence and in the absence of the very bulky base, 1-t-butyl-5-phenylimidazole, is also investigated. The title dimer, (DPA) Pd 2, shows fluorescence and phosphorescence in the ps and ms time scale, respectively, with a global intensity lower than that of the porphyrin monomer analogues. The fluorescence sensitivity towards dioxygen quenc…

chemistry.chemical_compoundAnthraceneQuenching (fluorescence)MonomerchemistryDimerGeneral ChemistryLuminescencePhotochemistryPhosphorescenceFluorescencePorphyrinJournal of Porphyrins and Phthalocyanines
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