In the present work, we synthesize Near Infrared (NIR)-emitting alloyed mercaptopropionic acid (MPA)-capped CdTeSe quantum dots (QDs) in a single-step one-hour process, without the use of an inert atmosphere or any pyrophoric ligands. The quantum dots are water soluble, non-toxic, and highly photostable and have high quantum yields (QYs) up to 84%. The alloyed MPA-capped CdTeSe QDs exhibit a red-shifted emission, whose color can be tuned between visible and NIR regions (608–750 nm) by controlling the Te:Se molar ratio in the precursor mixtures and/or changing the time reaction. The MPA-capped QDs were characterized by UV-visible absorption spectroscopy, fluorescence spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), and zeta potential measurements. Photostability studies were performed by irradiating the QDs with a high-power xenon lamp. The ternary MPA-CdTeSe QDs showed greater photostability than the corresponding binary MPA-CdTe QDs. We report the Förster resonance energy transfer (FRET) from the MPA-capped CdTeSe QDs as energy donors and Cyanine5 NHS-ester (Cy5) dye as an energy acceptor with efficiency (E) up to 95%. The distance between the QDs and dye (r), the Förster distance (R0), and the binding constant (K) are reported. Additionally, cytocompatibility and cell internalization experiments conducted on human cancer cells (HeLa) cells revealed that alloyed MPA-capped CdTeSe QDs are more cytocompatible than MPA-capped CdTe QDs and are capable of ordering homogeneously all over the cytoplasm, which allows their use as potential safe, green donors for biological FRET applications.
Polycyclic hydrocarbons constitute an important source of very dangerous pollutants. Different materials have been used as adsorbent for their removal, but they present difficulties in the separation process. The use of a material based on metal-organic framework (MOF) with large pores and high surface area and magnetic nanoparticles with superparamagnetic properties is an interesting strategy. In this work a magnetic composite based on MOF (MIL-101) and Fe3O4 magnetic nanoparticles (Fe3O4/MIL-101) was obtained by a simple synthesis method and used as adsorbent for the removal of anthracene. The composite was characterized by transmission electron microscopy, x-ray powder diffraction and vibrating sample magnetometer. The results showed that kinetic data followed a first-order model and equilibrium data were well fitted by the Langmuir model. The maximum adsorption capacity was 12.7 mg g−1 at pH 6 in 60 min of exposure. The composite was applied for the adsorption of anthracene in water samples reaching more than 95% of anthracene removal in 1 h of contact. The composite material was effectively separated using an external magnet, and no further centrifugation or filtration processes were needed. This composite is a great alternative to remove polycyclic hydrocarbons from water samples and has potential to extend to the removal of other contaminants.
The aminobenzamide–aminonaphthalimide fluorescent dyads allow the determination of Cu2+ and Hg2+ metal ion concentration from Förster Resonant Energy Transfer measurements.
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