Abstract
Mechanophores (mechanosensitive molecules) are usually activated by pulling them with covalently attached polymers. A rotaxane actuator offers a new geometry of activation as the macrocycle pushes against a stoppering mechanophore. Here we compare both pulling and pushing activations and show that pushing is more efficient and selective than pulling. We found that the pulling activation of a bulky furan/maleimide adduct occurs via two competing dissociation pathways: retrocycloaddition and heterolytic cleavage (generating a trityl cation in the process), while the same adduct only cleaves by retrocycloaddition during pushing activation. These results further demonstrate the efficacy and versatility of rotaxane actuators.
Original language | English |
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Pages (from-to) | 16381–16384 |
Journal | Journal of the American Chemical Society |
Volume | 146 |
Issue number | 24 |
Early online date | 7 Jun 2024 |
DOIs | |
Publication status | Published - 19 Jun 2024 |