Abstract
A symmetrically disubstituted derivative of the highly fluorescing and photostable rubicene was incorporated in a macrocycle using high dilution conditions and a hydroxyrubicene was functionalized with a modified aminobenzo-15-crown-5.
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APA
Smet, M., & Dehaen, W. (2000). Synthesis of crown ethers containing a rubicene moiety. Molecules, 5(3), 620–628. https://doi.org/10.3390/50300620
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