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      Pushing vs Pulling: The Unique Geometry of Mechanophore Activation in a Rotaxane Force Actuator

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      Journal of the American Chemical Society
      American Chemical Society

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          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.

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          Mechanically-induced chemical changes in polymeric materials.

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            Rotaxanes as Mechanochromic Fluorescent Force Transducers in Polymers

            The integration of mechanophores, motifs that transduce mechanical forces into chemical reactions, allows creating materials with stress-dependent properties. Typical mechanophores are activated by cleaving weak covalent bonds, but these reactions can also be triggered by other stimuli, and this renders the behavior unspecific. Here we show that this problem can be overcome by extending the molecular-shuttle function of rotaxanes to mechanical activation. A mechanically interlocked mechanophore composed of a fluorophore-carrying macrocycle and a dumbbell-shaped molecule containing a matching quencher was integrated into a polyurethane elastomer. Deformation of this polymer causes a fluorescence turn-on, due to the spatial separation of fluorophore and quencher. This process is specific, efficient, instantly reversible, and elicits an easily detectable optical signal that correlates with the applied force.
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              Cu(0)-Mediated Living Radical Polymerization: A Versatile Tool for Materials Synthesis

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                Author and article information

                Journal
                J Am Chem Soc
                J Am Chem Soc
                ja
                jacsat
                Journal of the American Chemical Society
                American Chemical Society
                0002-7863
                1520-5126
                07 June 2024
                19 June 2024
                : 146
                : 24
                : 16381-16384
                Affiliations
                [1]Department of Chemistry, University of Manchester , Oxford Road, Manchester, M13 9PL, United Kingdom
                Author notes
                Author information
                https://orcid.org/0000-0003-2670-6370
                Article
                10.1021/jacs.4c05168
                11191692
                38848593
                9c3cbaf3-c719-44b1-9017-304d6dc100b6
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 15 April 2024
                : 05 June 2024
                : 03 June 2024
                Funding
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: NA
                Funded by: China Scholarship Council, doi 10.13039/501100004543;
                Award ID: NA
                Funded by: Royal Society, doi 10.13039/501100000288;
                Award ID: NA
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: EP/X023788/1
                Categories
                Communication
                Custom metadata
                ja4c05168
                ja4c05168

                Chemistry
                Chemistry

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