Here we describe a unique process that achieves complete defluorination and decomposition of perfluorinated compounds (PFCs) which comprise one of the most recalcitrant and widely distributed classes of toxic pollutant chemicals found in natural environments. Photogenerated hydrated electrons derived from 3-indole-acetic-acid within an organomodified clay induce the reductive defluorination of co-sorbed PFCs. The process proceeds to completion within a few hours under mild reaction conditions. The organomontmorillonite clay promotes the formation of highly reactive hydrated electrons by stabilizing indole radical cations formed upon photolysis, and prevents their deactivation by reaction with protons or oxygen. In the constrained interlayer regions of the clay, hydrated electrons and co-sorbed PFCs are brought in close proximity thereby increasing the probability of reaction. This novel green chemistry provides the basis for in situ and ex situ technologies to treat one of the most troublesome, recalcitrant and ubiquitous classes of environmental contaminants, i.e., PFCs, utilizing innocuous reagents, naturally occurring materials and mild reaction conditions.
A novel lysosome-targeting ratiometric fluorescent probe (CQ-Lyso) based on the chromenoquinoline chromorphore has been developed for the selective and sensitive detection of intracellular pH in living cells. In acidic media, the protonation of the quinoline ring of CQ-Lyso induces an enhanced intramolecular charge transfer (ICT) process, which results in large red-shifts in both the absorption (104 nm) and emission (53 nm) spectra which forms the basis of a new ratiometric fluorescence pH sensor. This probe efficiently stains lysosomes with high Pearson's colocalization coefficients using LysoTrackerDeep Red (0.97) and LysoTrackerBlue DND-22 (0.95) as references. Importantly, we show that CQ-Lyso quantitatively measures and images lysosomal pH values in a ratiometric manner using single-wavelength excitation.
Surface-enhanced Raman scattering (SERS) can provide fingerprint information of analyte molecules with unparalleled sensitivity. However, quantitative analysis using SERS has remained one of the major challenges owing to the difficulty of obtaining reproducible SERS substrates with high-density hotspots. Here, we report the rational design and fabrication of a binary thiol-capped gold nanoparticle (AuNP) monolayer film (MLF) as a substrate for highly sensitive and quantitative SERS analysis. The two thiol ligands chemically bonded to the AuNPs play different roles: dodecanethiol with a long alkyl chain controls the interparticle gaps and electromagnetic coupling among AuNPs and 4-mercaptopyridine works as a Raman internal standard (IS). The binary thiol-capped AuNPs can self-assemble into an ordered MLF with high-density hotspots and uniformly distributed IS. The asprepared MLF has been demonstrated as a reliable SERS substrate for quantitative detection of fungicide malachite green in aqueous solution, with a high enhancement factor (up to 3.3 × 10 7 ) and a low detection limit (100 pM). Moreover, the MLF SERS substrate is flexible and transparent, which has enabled in situ detection of trace fungicide residues in a shrimp tissue.
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