Open AccessThis article is
- freely available
Synthesis of Crown Ethers Containing a Rubicene Moiety
Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200F, 3001 Heverlee Belgium
* Author to whom correspondence should be addressed.
Received: 10 February 2000; in revised form: / Accepted: 14 March 2000 / Published: 22 March 2000
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.
Keywords: rubicene; crown ethers; macrocycle synthesis
Article StatisticsClick here to load and display the download statistics.
Notes: Multiple requests from the same IP address are counted as one view.
Cite This Article
MDPI and ACS Style
Smet, M.; Dehaen, W. Synthesis of Crown Ethers Containing a Rubicene Moiety. Molecules 2000, 5, 620-628.
Smet M, Dehaen W. Synthesis of Crown Ethers Containing a Rubicene Moiety. Molecules. 2000; 5(3):620-628.
Smet, Mario; Dehaen, Wim. 2000. "Synthesis of Crown Ethers Containing a Rubicene Moiety." Molecules 5, no. 3: 620-628.