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High Quantum Yields (high + quantum_yield)
Selected AbstractsDesign, characterization, and utilization of a fast fluorescence derivatization reaction utilizing o -phthaldialdehyde coupled with fluorescent thiolsELECTROPHORESIS, Issue 7 2007Suminda Hapuarachchi Abstract We have developed a chemical derivatization scheme for primary amines that couples the fast kinetic properties of o -phthaldialdehyde (OPA) with the photophysical properties of visible, high quantum yield, fluorescent dyes. In this reaction, OPA is used as a cross-linking reagent in the labeling reaction of primary amines in the presence of a fluorescent thiol, 5-((2-(and-3)- S -(acetylmercapto)succinoyl)amino)fluorescein (SAMSA fluorescein), thereby incorporating fluorescein (,,=,78,000,M,1, quantum yield of 0.98) into the isoindole product. Detection is based on excitation and emission of the incorporated fluorescein using the 488,nm laser line of an Ar+ laser rather than the UV-excited isoindole, thereby eliminating the UV light sources for detection. Using this method, we have quantitatively labeled biologically important primary amines in less than 10,s. Detection limits for analysis of glutamate, glycine, GABA, and taurine were less than 2,nM. We present the characterization of OPA/SAMSA-F reaction and the potential utility of the derivatization reaction for dynamic chemical monitoring of biologically relevant analytes using CE. [source] Cationic Oligofluorene-Substituted Polyhedral Oligomeric Silsesquioxane as Light-Harvesting Unimolecular Nanoparticle for Fluorescence Amplification in Cellular ImagingADVANCED MATERIALS, Issue 5 2010Kan-Yi Pu A new bottom-up strategy is used to construct water-soluble organic/inorganic fluorescent unimolecular nanoparticles based on polyhedral oligomeric silsesquioxane (POSS) and conjugated oligoelectrolyte. Their high quantum yield, good cytocompatibility, and unique whole-cell permeability could serve as a light-harvesting energy donor to amplify the intracellular dye fluorescence for high-quality biological imaging through fluorescence resonance energy transfer (see image). [source] Effects of lodide on the Fluorescence and Activity of the Hydroperoxyflavin Intermediate of Vibrio harveyi Luciferase,PHOTOCHEMISTRY & PHOTOBIOLOGY, Issue 2 2005Shouqin Huang ABSTRACT The 4a-hydroperoxy-4a,5-dihydroFMN intermediate (II or HFOOH) of Vibrio harveyi luciferase is known to transform from a low quantum yield IIx to a high quantum yield (,max 485 nm, uncorrected) IIy fluorescent species on exposure to excitation light. Similar results were observed with II prepared from the ,H44A luciferase mutant, which is very weak in bioluminescence activity. Because of the rapid decay of the ,H44A II, its true fluorescence was obscured by the more intense 520 nm fluorescence (uncorrected) from its decay product oxidized flavin mononucleotide (FMN). Potassium iodide (KI) at 0.2 M was effective in quenching the FMN fluorescence, leaving the 485 nm fluorescence of II from both the wild-type (WT) and ,H44A luciferase readily detectable. For both II species, the luciferase-bound peroxyflavin was well shielded from KI quenching. KI also enhanced the decay rates of both the WT and ,H44A II. For ,H44A, the transformation of IIx to IIy can be induced by KI in the dark, and it is proposed to be a consequence of a luciferase conformational change. The WT II formed a bioluminescence-inactive complex with KI, resulting in two distinct decay time courses based on absorption changes and decreases of bioluminescence activity of II. [source] A simple light-emitted diode-induced fluorescence detector using optical fibers and a charged coupled device for direct and indirect capillary electrophoresis methodsELECTROPHORESIS, Issue 9 2006David Arráez-Román Abstract We constructed a simple fluorescence detector for both direct and indirect CE methods using a blue light-emitted diode (470,nm) as excitation source, a bifurcated optical fiber as a waveguide, and a CCD camera as a detector. The connection of all the components is fairly easy even for nonexperts and the use of a CCD camera improves the applicability of this detector compared to the others using PMTs because it permits the recording of 2-D electropherograms or phosphorescence measurements. This detector provides a compact, low cost, and rapid system for the determination of native fluorescence compounds which have high quantum yields by CE with direct fluorescence detection, showing an LOD of 2.6×10,6,M for fluorescein; the determination of fluorescence derivative compounds by CE with direct fluorescence detection, showing an LOD of 1.6×10,7,M for FITC-labeled 1,6-diaminohexane; and nonfluorescence compounds by CE with indirect fluorescence detection with an LOD of 2.7×10,6,M for gallic acid. [source] Versatile, Benzimidazole/Amine-Based Ambipolar Compounds for Electroluminescent Applications: Single-Layer, Blue, Fluorescent OLEDs, Hosts for Single-Layer, Phosphorescent OLEDsADVANCED FUNCTIONAL MATERIALS, Issue 16 2009Chih-Hsin Chen Abstract A series of compounds containing arylamine and 1,2-diphenyl-1H -benz[d]imidazole moieties are developed as ambipolar, blue-emitting materials with tunable blue-emitting wavelengths, tunable ambipolar carrier-transport properties and tunable triplet energy gaps. These compounds possess several novel properties: (1) they emit in the blue region with high quantum yields; (2) they have high morphological stability and thermal stability; (3) they are capable of ambipolar carrier transport; (4) they possess tunable triplet energy gaps, suitable as hosts for yellow-orange to green phosphors. The electron and hole mobilities of these compounds lie in the range of 0.68,144,×,10,6 and 0.34,147,×,10,6,cm2 V,1 s,1, respectively. High-performance, single-layer, blue-emitting, fluorescent organic light-emitting diodes (OLEDs) are achieved with these ambipolar materials. High-performance, single-layer, phosphorescent OLEDs with yellow-orange to green emission are also been demonstrated using these ambipolar materials, which have different triplet energy gaps as the host for yellow-orange-emitting to green-emitting iridium complexes. When these ambipolar, blue-emitting materials are lightly doped with a yellow-orange-emitting iridium complex, white organic light-emitting diodes (WOLEDs) can be achieved, as well by the use of the incomplete energy transfer between the host and the dopant. [source] Synthesis and properties of conjugated polymers containing 3,9- and 2,9-linked carbazole units in the main chainJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 14 2009Kosaku Tamura Abstract Novel conjugated polymers containing 3,9- or 2,9-linked carbazole units in the main chain were synthesized by the polycondensation of ethynyl- and iodo-substituted 9-arylenecarbazolylene monomers, and their optical and electrical properties were studied. Polymers with weight-average molecular weights of 3400,12,000 were obtained in 76,99% yields by the Sonogashira coupling polycondensation in piperidine or tetrahydrofuran (THF)/piperidine at 30 °C for 48 h. All the 3,9-linked polymers absorbed light around 300 nm. The para -phenylene-linked polymer also absorbed light around 350 nm, while meta -phenylene-linked one did not. The 3,9-linked polymers absorbed light at a wavelength longer than the 2,9-linked one. The polymers emitted blue fluorescence with high quantum yields (0.21,0.78) upon excitation at the absorption maxima. The polymers were oxidized around 0.6 V, and reduced around 0.5 V. Poly(1) showed the dark conductivity of 3.7 × 10,11 S/cm (103 V/cm). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3506,3517, 2009 [source] Photophysical and electrochemical characterization of new poly(arylene vinylene) copolymers containing quinoline or bisquinoline segmentsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 13 2009John A. Mikroyannidis Abstract Four new fluorescent conjugated vinylene-copolymers incorporating quinoline or bisquinoline segments along the backbone were synthesized by Heck coupling. Three of them were fluorenevinylene-copolymers and contained quinoline (PQFV, PQFVT) or bisquinoline segments (PBQFV). One of them (PBQPV) was phenylenevinylene-copolymer and contained bisquinoline segments. All the copolymers were soluble in common organic solvents and had relatively low glass transition temperature (Tg = 50,56 °C for fluorenevinylenes and Tg < 25 °C for phenylenevinylene). In THF solutions, the quinoline-containing copolymers showed absorption maxima at 411,420 nm while the bisquinoline-containing ones exhibited maxima at 357,361 nm. The emission maxima of solutions were 465,490 nm. The copolymers showed high quantum yields up to 64%. The films exhibited absorption and emission maxima in the range of 371,437 nm and 480,521 nm, respectively. All copolymers revealed reversible reduction with electron affinity of 2.66,3.53 eV and irreversible oxidation scans with ionization potential of 5.39,5.53 eV. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3370,3379, 2009 [source] Advancing the Solid State Properties of Metallo-Supramolecular Materials: Poly(, -caprolactone) Modified , -Conjugated Bis(terpyridine)s and their Zn(II) Based Metallo-PolymersMACROMOLECULAR RAPID COMMUNICATIONS, Issue 20 2008Andreas Winter Abstract A set of rigid , -conjugated bis(terpyridine) macroligands with poly(, -caprolactone) (pCL) on their side chains was synthesized and investigated. The introduced pCL chains gave rise to enhanced processability and film-forming properties of the materials. Blue photoluminescence with high quantum yields was observed in dilute solution and in the solid state, indicating that intermolecular aggregation of the , -conjugated systems was effectively suppressed. The macroligands were further used for coordination with zinc(II) ions leading to new metallo-polymers with high solubility, improved film-forming behavior and promising photophysical properties with respect to potential OLED applications. [source] New , -Conjugated Polymers Containing 1,3,5-Triazine Units in the Main Chain: Synthesis and Optical and Electrochemical Properties of the Polymers,MACROMOLECULAR RAPID COMMUNICATIONS, Issue 12 2005Shijie Ren Abstract Summary: Three new soluble , -conjugated polymers containing 1,3,5-triazine units in the main chain, Pa,Pc, were synthesized. The polymers showed optical properties in solution that were mainly dependant on the properties of the substituting R groups, on the triazine ring. Hence, Pa and Pb (R,=,H and OCH3, respectively) showed blue photoluminescent (PL) emission with high quantum yields (QY) even in polar solvents, whereas Pc (R,=,N,N -dimethylamino) gave green-blue PL emission with very low QY. The PL spectra of the polymers in solution were concentration and polarity dependent, which suggested the formation of an exciplex. The three new soluble , -conjugated polymers containing 1,3,5-triazine units in the main chain synthesized here. [source] Substituent effects on the photofading of disperse azo dyes on poly(ethylene terephthalate) substrateCOLORATION TECHNOLOGY, Issue 3 2010Yasuyo Okada The relationships between the chemical structures and oxidative fading of the disperse azo dyes, p -nitrophenylazo- and benzothiazoleazo-anilines, on poly(ethylene terephthalate) substrate are discussed in terms of the parameters k0,i (rate constants of reaction towards 1O2) and fi (photosensitivity), the molecular parameters of molecular orbital theory and substituents in the diazo and coupling components, on the assumption that the initial rates of oxidative fading are proportional to the product of k0,i and fi. 2-Methoxy-5-acetylamino- N -substituted aniline couplers exhibited large fi values. 2-Chloro and 4-nitro substituents of aniline diazo components exhibited small fi values or high quantum yields of internal conversion, while 4-nitro substituent did not. A close correlation between N -substituents and light fastness, proposed by Müller and supplemented by Dawson, demonstrates the applicability of frontier orbital theory, through the highest occupied molecular orbital (HOMO) energy of the dyes, to the analysis of oxidative fading. Dyes with N -2-cyanoethyl substituents, which gave a lower HOMO energy, also exhibited superior light fastness compared with N -2-hydroxyethyl substituents. [source] | |||||||||||||||||||||||||