Synfacts 2007(10): 1043-1043  
DOI: 10.1055/s-2007-968988
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag Stuttgart · New York

Fluorescent J-Aggregates

Contributor(s): Timothy M. Swager, Koushik Venkatesan
T. E. Kaiser, H. Wang, V. Stepanenko, F. Würthner*
Universität Würzburg, Germany
Further Information

Publication History

Publication Date:
07 November 2007 (online)

Significance

The authors report a highly fluorescent J-aggregate assembled from the highly stable fluorophore perylene bisimide. The unprecedented packing of perylene bisimide dyes in a strongly slipped arrangement was tailored by twisting of the perylene core enforced by bay substituents, the attachment of trialkoxyphenyl ­wedges, and head-to-tail alignment of the dyes through hydrogen-bonding interactions. Cleavage of the methyl ether groups in the bay substituents and the N-benzyl groups in the imide positions with BBr3 in anhydrous dichloromethane provided the deprotected perylene bisimide intermediate. Subsequent esterification with 3,4,5-tridodecyloxybenzoic acid afforded the target dye.