Journal
CHEMICAL SCIENCE
Volume 10, Issue 29, Pages 7076-7081Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9sc01035a
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Funding
- National Key Research and Development Program of China [2016YFA0602900]
- National Natural Science Foundation of China [21490572, 21672072]
- Guangdong Natural Science Foundation [2018B030308007]
- Pearl River S&T Nova Program of Guangzhou [201610010160]
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A novel strategy has been established to assemble a series of single (Z)- or (E)-1H-isoindole derivatives through selectively and sequentially activating carbon-nitrogen triple bonds in a multicomponent system containing various nucleophilic and electrophilic sites. The reaction provides efficient access to structurally unique fluorophores with aggregation-induced emission characteristics. These new fluorophores show fluorescence wavelengths and efficiencies that can be modulated and have excellent potential to specifically light up lipid droplets (LDs) in living cells with bright fluorescence, low cytotoxicity and better photostability than commercially available LD-specific dyes.
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