Light-Driven Controllable Cis-trans Isomerization in a Cycloparaphenylene Dimer Bridged by 9,9′-Bifluorenylidene

Abstract

This work reports the synthesis and distinct photoisomerization of configurationally stable isomers of a cycloparaphenylene (CPP) dimer, bridged by a 9,9′-bifluorenylidene linker. Bidirectional photo-switching is achieved: a synergistic photoacid-catalyzed process drives the trans-to-cis conversion, while a light-induced electron-transfer pathway, enables efficient cis-to-trans isomerization.

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Article information

Article type
Communication
Submitted
09 Feb 2026
Accepted
23 Mar 2026
First published
24 Mar 2026

Chem. Commun., 2026, Accepted Manuscript

Light-Driven Controllable Cis-trans Isomerization in a Cycloparaphenylene Dimer Bridged by 9,9′-Bifluorenylidene

D. Zhang, K. Lan, X. Zhang, J. Jiang and C. Cheng, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC00869K

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