Search results for "Fluorescence"

showing 10 items of 2463 documents

Rapid fluorimetric assay for primary amine groups in water samples

2003

Bond Elut C(18) solid-phase extraction cartridges were used for pre-concentration followed by derivatization with o-phthaldialdehyde-N-acetylcysteine (OPA-NAC) of primary amines in water. Optimal conditions were: conditioning the cartridges with borate buffer pH 10.4, retention of the primary amines, addition of the OPA-NAC(3.7 mmol L(-1)) 1:1 molar ratio and borate buffer pH 8, elution of the isoindol with MeOH-borate buffer (9:1) pH 10.2 and fluorescence measurement. The equations of the calibration graphs for methylamine, ethylamine, propylamine, butylamine, pentylamine, and beta-phenylethylamine at lambda(excitation)=330 nm and lambda(emission)=440 nm, in the optimal conditions are pres…

chemistry.chemical_compoundMolar concentrationChromatographyChemistryButylamineMethylamineFluorescence spectrometryPropylamineSolid phase extractionPentylamineDerivatizationBiochemistryAnalytical ChemistryAnalytical and Bioanalytical Chemistry
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(E,E,E)-4,4′-Distyrylstilbenes – Synthesis, Photophysics, Photochemistry and Phase Behavior

2008

The fluorescence quantum yields F(n) of oligo[2,5-bis(propyloxy)-1,4-phenylenevinylene]s (1b) reach for the trimer (n = 3) in solution a maximum of 86 %, which is almost twice as high as for the monomer (n = 1) and the octamer or undecamer (n = 8, 11). The latter represent the convergence limit of 46 %. 4-Mono-, 3,4-di- or 3,4,5-trisubstituted terminal phenyl rings in the trimers 6a–f do not lead to calamitic or phasmidic liquid crystals; however, 2,3,4-trisubstitution with hexyloxy groups (6h) and even with OCH3 groups (6g) effects LC formation. Irradiation with energy-rich UV light provokes a crosslinking of the originally conjugated chains. In the case of 6c, a chemo- and stereoselective…

chemistry.chemical_compoundMonomerLiquid crystalChemistryPhase (matter)Organic ChemistryStereoselectivityTrimerPhysical and Theoretical ChemistryConjugated systemPhotochemistryCondensation reactionFluorescenceEuropean Journal of Organic Chemistry
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Three independent channel nanohybrids as fluorescent probes

2015

A properly designed pyrene-capped CdSe/ZnS nanohybrid can act as a three-channel fluorescent sensor due to the independent emission of the pyrene monomer and excimer as well as that of the nanoparticle. As proof of principle, it was tested for a simple and rapid quantification of TNT in the presence of interferents of the same chemical family.

chemistry.chemical_compoundMonomerMaterials sciencechemistryGeneral Chemical EngineeringPyreneNanoparticleNanotechnologyGeneral ChemistryExcimerFluorescenceRSC Advances
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Investigations of the Microstructure of Lipid Interface Films

1990

The phase behaviour of phospholipid monolayers at electrolyte/gas interfaces is studied by fluorescence microscopy. At the LE/LC phase transition, phase separation leads to a Wigner-type lattice structure. The observations are quantified using digital image processing. The results show that the phase transition comprises three different regimes.

chemistry.chemical_compoundPhase transitionMaterials sciencechemistryPhase (matter)MonolayerFluorescence microscopePhospholipidAnalytical chemistryCrystal structureElectrolyteMicrostructure
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ChemInform Abstract: Diaryldistyrylpyrazines: Solvatochromic and Acidochromic Fluorophores.

2014

Diaryldimethylpyrazines are the starting materials for the synthesis of C2-symmetric donor- or acceptor-substituted distyrylpyrazines. The optical properties of these cruciform-shaped dyes are dominated by the distyrylpyrazine units; the photophysics is controlled by the styryl substitution, the diaryl substituents on the central pyrazine only having a small effect. Protonation occurs on the pyrazine and/or lateral amines or azines, thereby altering the absorption and emission properties. Hypso- and bathochromism as well as fluorescence quenching depend on the nature of the terminal substituent. This, and a significant positive solvatochromism of the fluorescence, allow optical sensing of t…

chemistry.chemical_compoundPyrazinechemistryPolarity (physics)Optical sensingSolvatochromismSubstituentProtonationGeneral MedicineAbsorption (chemistry)PhotochemistryFluorescenceChemInform
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Scintillation Measurements at Very High Solute Concentrations; Self Quenching-Structure Correlatios

1968

Abstract Measurements of the relative scintillation yields of some liquid organic systems were carried out with several highly soluble scintillator solutes. Self quenching was observed at high concentrations with some of the solutes, but not with others. The results were correlated with the ability of the solute molecules to come together, in a special configuration, close enough to form an association. A study of the atomic models of the solute molecules showed that those moleculeswith chromophor systems which were non-coplanar, or co-planar but shielded by substituent groups, did not produce self quenching. However, those solute molecules with unprotected co-planar chromophor systems did …

chemistry.chemical_compoundScintillationQuenching (fluorescence)chemistryAtomic theoryOrganic systemsSubstituentAnalytical chemistryMoleculePhosphorScintillatorMolecular Crystals
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A Bichromophore Based on Perylene and Terrylene for Energy Transfer Studies at the Single-Molecule Level

1999

A functionalized dialkylperylene and a modified terrylenetetracarboxdiimide (TTCDI) were joined by a hexanediyl spacer. The resulting bichromophoric molecule 1 (R = 4-tert-butylphenoxy) is a suitable model system for donor–acceptor energy transfer studies at the single-molecule level.

chemistry.chemical_compoundUltraviolet visible spectroscopychemistryEnergy transferOrganic ChemistryMoleculeModel systemGeneral ChemistryPhotochemistryCatalysisPeryleneFluorescence spectroscopyChemistry - A European Journal
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Synthesis and Electronic Spectra of Substitutedp-Distyrylbenzenes for the Use in Light-Emitting Diodes

2000

The influence of substitution on the absorption and Luminescence spectra of oligo(phenylenevinylene)s has been studied using distyrylbenzene (DSB) as a model compound. The degree, character, and pattern of substitution was varied systematically, altering the electronic properties of the DSB, the wavelength of the emitted light could be tuned over a range of 100 nm. The syntheses of 6b—h were performed by twofold Wittig Horner-olefinations of bisphoshonates 1a, b with substituted benzaldehydes 2a—i, 6ivia Heck-reaction of the dibromosulfonylbenzene 3, 6k by Siegrist-reaction of 4 with N-phenylbenzaldimine and the Knoevenagel-reaction of benzyl cyanide with 5 led to 6l.

chemistry.chemical_compoundWavelengthUltraviolet visible spectroscopyChemistrylawWittig reactionBenzyl cyanideAbsorption (electromagnetic radiation)PhotochemistryFluorescence spectroscopySpectral lineLight-emitting diodelaw.inventionJournal für praktische Chemie
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Use of fluorescent dyes for developing latent lip prints

2004

Advances in the sensitivity of techniques used to examine latent prints (finger or labial) make it necessary to find more effective methods of locating prints on different surfaces. The most difficult surfaces are those which are porous or multicoloured, in which case the developed print may not be easily seen. This study analyses the effectiveness of two fluorescent dyes, Nile Blue and Nile Red, in developing both recent and older latent lip prints on porous and multicoloured surfaces. The results indicate that Nile Red is a very effective reagent for the development of latent lip prints on difficult surfaces of this type.

chemistry.chemical_compoundchemistryChemistry (miscellaneous)Materials Science (miscellaneous)General Chemical EngineeringeducationNile redLIP PRINTSNanotechnologyNile blueFluorescenceColoration Technology
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ChemInform Abstract: Synthesis of Tetrasubstituted 4,4′-Biimidazoles.

2012

Highly substituted 4,4′-biimidazoles were synthesized, in good to excellent yields, through a multicomponent imidazole ring synthesis by using imidazol-4-yl-ethane-1,2-diones as starting materials. The obtained compounds were preliminarily tested as chromogenic and fluorescent sensors for heavy metals.

chemistry.chemical_compoundchemistryChromogenicImidazoleHeavy metalsGeneral MedicineRing (chemistry)FluorescenceCombinatorial chemistryChemInform
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