Synthesis of Crown Ethers Containing a Rubicene Moiety

doi:10.3390/50300620

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

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Synthesis of Crown Ethers Containing a Rubicene Moiety

Mario Smet and Wim Dehaen*

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

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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

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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.

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