Gold nanoclusters prepared with a controlled amount of Ag exhibit intense fluorescence with a quantum yield of ~16% and a "quasi-monoexponential" long lifetime of >200 ns. Characterization of the luminescent probes indicates high photostability and easy detection in cells. Additionally, fluorescence enhancement in the presence of proteins was found.
New types of fluorescent platinum nanoclusters (λ max. = 570 nm) have been synthesized using glutathione for ligand etching. These nanoclusters are mainly in the oxidation state Pt I (90%) exhibiting an intense fluorescence signal (QY∼17%) in the yellow region and lead to the formation of blue-emitting species for a long etching time process.
The asymmetric substituted BODIPY
dye 4,4-difluoro-1,3-dimethyl-4-bora-3a,4a-diaza-s-indacene
crystallizes in three different crystal habits, that is, as needles
(I), leaves (II), or microcrystalline sublimed
crystals (III). All crystals share the same crystal structure
but exhibit varying solid-state fluorescence from yellow-orange to
deep red. The crystal structure mainly consists of one-dimensional
chains of J-aggregates which leads to excitonic luminescence at λ
= 600 nm. The point-dipole approximation is used to calculate the
excitonic splitting to a value of 3300 cm–1, which
is in good agreement with the experimental observations. The influence
of the macroscopic appearance on the luminescence properties is discussed
in terms of reflectivity of the surface and reabsorption within the
material. It turns out that the long-range order modulates the solid-state
luminescence due to the small Stokes shift of the dye.
Fluorescence-detected circular dichroism (FDCD) spectroscopy is applied for the first time to supramolecular host-guest and host-protein systems and compared to the more known electronic circular dichroism (ECD). We find that...
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