Premium
Folded Perylene Diimide Loops as Mechanoresponsive Motifs
Author(s) -
Traeger Hanna,
Sagara Yoshimitsu,
Kiebala Derek J.,
Schrettl Stephen,
Weder Christoph
Publication year - 2021
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.202105219
Subject(s) - excimer , perylene , diimide , intramolecular force , moiety , photochemistry , polymer , intermolecular force , fluorescence , materials science , acrylate , supramolecular chemistry , supramolecular polymers , polymer chemistry , chemistry , molecule , stereochemistry , copolymer , organic chemistry , optics , physics , composite material
A supramolecular mechanophore that can be integrated into polymers and indicates deformation by a fluorescence color change is reported. Two perylene diimides (PDIs) were connected by a short spacer and equipped with peripheral atom transfer polymerization initiators. In the idle state, the motif folds into a loop and its emission is excimer dominated. Poly(methyl acrylate) (PMA) chains were grown from the motif and the mechanophore‐containing polymer was blended with unmodified PMA to afford materials that display a visually discernible fluorescence color change upon deformation, which causes the loops to unfold. The response is instant, and correlates linearly with the applied strain. Experiments with a reference polymer containing only one PDI moiety show that looped mechanophores that display intramolecular excimer formation offer considerable advantages over intermolecular dye aggregates, including a concentration‐independent response, direct signaling of mechanical processes, and a more pronounced optical change.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom