Journal
NATURE CHEMISTRY
Volume 5, Issue 2, Pages 110-114Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/NCHEM.1540
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- US Army Research Laboratory
- Army Research Office [W911NF-07-1-0409]
- National Science Foundation [DMR-1122483]
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Mechanical forces along a polymer backbone can be used to bring about remarkable reactivity in embedded mechanically active functional groups, but little attention has been paid to how a given polymer backbone delivers that force to the reactant. Here, single-molecule force spectroscopy was used to directly quantify and compare the forces associated with the ring opening of gem-dibromo and gem-dichlorocyclopropanes affixed along the backbone of cis-polynorbornene and cis-polybutadiene. The critical force for isomerization drops by about one-third in the polynorbornene scaffold relative to polybutadiene. The root of the effect lies in more efficient chemomechanical coupling through the polynorbornene backbone, which acts as a phenomenological lever with greater mechanical advantage than polybutadiene. The experimental results are supported computationally and provide the foundation for a new strategy by which to engineer mechanochemical reactivity.
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