Molecules 2000, 5(3), 620-628; doi:10.3390/50300620
Article

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; Accepted: 14 March 2000 / Published: 22 March 2000
PDF Full-text Download PDF Full-Text [39 KB, uploaded 7 October 2008 08:55 CEST]
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 Statistics

Load and display the download statistics.

Citations to this Article

Cite This Article

MDPI and ACS Style

Smet, M.; Dehaen, W. Synthesis of Crown Ethers Containing a Rubicene Moiety. Molecules 2000, 5, 620-628.

AMA Style

Smet M, Dehaen W. Synthesis of Crown Ethers Containing a Rubicene Moiety. Molecules. 2000; 5(3):620-628.

Chicago/Turabian Style

Smet, Mario; Dehaen, Wim. 2000. "Synthesis of Crown Ethers Containing a Rubicene Moiety." Molecules 5, no. 3: 620-628.

Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert