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

Synthesis of Crown Ethers Containing a Rubicene Moiety

 and *
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 rubicene; crown ethers; macrocycle synthesis
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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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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