Issue 37, 2024

Synthesis of anthracene-bridged expanded rosarin

Abstract

The newly synthesized precursor 1,8-di(1H-pyrrol-2-yl)anthracene was condensed with pentafluorobenzaldehyde under acid-catalyzed conditions to afford the first example of a unique anthracenyl-bridged rosarin. The X-ray structure revealed a coil-like arrangement of three dipyrromethene moieties and three anthracenyl units in the rosarin framework, which exhibits a weak fluorescence at 676 nm.

Graphical abstract: Synthesis of anthracene-bridged expanded rosarin

Supplementary files

Article information

Article type
Communication
Submitted
02 Aug 2024
Accepted
21 Aug 2024
First published
28 Aug 2024

Org. Biomol. Chem., 2024,22, 7607-7611

Synthesis of anthracene-bridged expanded rosarin

B. Yadav and M. Ravikanth, Org. Biomol. Chem., 2024, 22, 7607 DOI: 10.1039/D4OB01283F

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