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Multimodal mechanophores that react under mechanical force to produce discrete product states with uniquely coupled absorption properties are interesting targets for the design of force-sensing polymers. Herein, we investigate the reactivity of a 2H-bis-naphthopyran mechanophore that generates thermally persistent mono-merocyanine and bis-merocyanine products upon mechanical activation in solution using ultrasonication, distinct from the thermally reversible products generated photochemically. We demonstrate that a force-mediated ester C(O)–O bond scission reaction following ring opening establishes an intramolecular hydrogen bond, locking one merocyanine subunit in the open form. Model compound studies suggest that this locked subunit confers remarkable thermal stability to bis-merocyanine isomers possessing a trans exocyclic alkene on the other subunit, implicating the formation of an unusual trans merocyanine isomer as the product of mechanochemical activation. Density functional theory calculations unexpectedly predict a thermally reversible retro-cyclization reaction of the bis-merocyanine species that could explain the mechanochemical generation of the unusual trans merocyanine isomer.
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Validation of an accurate and expedient initial rates method for characterizing mechanophore reactivity
Understanding structure–mechanochemical reactivity relationships is important for informing the rational design of new stimuli-responsive polymers. To this end, establishing accurate reaction kinetics for mechanophore activation is a key objective. Here, we validate an initial rates method that enables the accurate and rapid determination of rate constants for ultrasound-induced mechanochemical transformations. Experimental reaction profiles are well-aligned with theoretical models, which support that the initial rates method effectively deconvolutes the kinetics of specific mechanophore activation from the competitive process of nonspecific chain scission.
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- Award ID(s):
- 2145791
- PAR ID:
- 10491095
- Publisher / Repository:
- American Chemical Society
- Date Published:
- Journal Name:
- ACS Macro Letters
- Volume:
- 12
- Issue:
- 4
- ISSN:
- 2161-1653
- Page Range / eLocation ID:
- 440 to 445
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1021/acsmacrolett.3c00054
