0000000000273950

AUTHOR

Uwe Pischel

0000-0001-8893-9829

showing 3 related works from this author

Unconventional Fluorescence Quenching in Naphthalimide-Capped CdSe/ZnS Nanoparticles

2013

Core–shell (CS) CdSe/ZnS quantum dots (QD) capped with ligands that possess a mercapto or an amino group and a naphthalimide (NI) as chromophore unit, linked by a short ethylene chain (CS@S–NI and CS@H2N–NI, respectively), have been synthesized and fully characterized by infrared and nuclear magnetic resonance spectroscopies, high-resolution transmission electron microscopy, and voltammetry as well as by steady-state absorption and emission spectroscopies. The organic ligands HS–NI and H2N–NI act as bidentate ligands, thereby causing a drastic decrease in the QD emission. This was particularly evident in the case of CS@S–NI. This behavior has been compared with that of commercially availabl…

DenticityChemistryLigandKineticsNanoparticleChromophorePhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyTransmission electron microscopyQuantum dotPhysical and Theoretical ChemistryAbsorption (chemistry)The Journal of Physical Chemistry C
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Diastereomeric Differentiation in the Quenching of Excited States by Hydrogen Donors

2003

chemistry.chemical_classificationKetoneQuenching (fluorescence)HydrogenInorganic chemistryDiastereomerHydrogen transferchemistry.chemical_elementGeneral ChemistryPhotochemistryCatalysischemistryExcited stateLaser chemistryAngewandte Chemie International Edition
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Electronic and Functional Scope of Boronic Acid Derived Salicylidenehydrazone (BASHY) Complexes as Fluorescent Dyes

2017

[EN] A series of boronic acid derived salicylidenehydrazone (BASHY) complexes was prepared and photophysically characterized. The dye platform can be modified by (a) electronic tuning along the cyanine-type axis via modification of the donor-acceptor pair and (b) functional tuning via the boronic acid residue. On the one hand, approach (a) allows the control of photophysical parameters such as Stokes shift, emission color, and two-photon absorption (2PA) cross section. The resulting dyes show emission light-up behavior in nonpolar media and are characterized by high fluorescence quantum yields (ca. 0.5-0.7) and brightness (ca. 35000-40000 M-1 cm(-1)). Moreover, the 2PA cross sections reach …

BrightnessDesignFluorophores010402 general chemistryPhotochemistry01 natural sciencessymbols.namesakechemistry.chemical_compoundResidue (chemistry)ChromophoreMolecular logicStokes shiftMoietyPROYECTOS DE INGENIERIABodipy dyes2-Photon absorptionEnhancement010405 organic chemistryChemistryOrganic ChemistryChromophoreFluorescence0104 chemical sciences3. Good healthsymbolsSurface modificationProbesHighly fluorescentDerivativesBoronic acidThe Journal of Organic Chemistry
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