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1. Flyby reaction trajectories: Chemical dynamics under extrinsic force

   https://doi.org/10.1126/science.abi7609  

   Liu, Yun; Holm, Soren; Meisner, Jan; Jia, Yuan; Wu, Qiong; Woods, Toby J.; Martinez, Todd J.; Moore, Jeffrey S. (July 2021, Science)

   null (Ed.)

   Dynamic effects are an important determinant of chemical reactivity and selectivity, but the deliberate manipulation of atomic motions during a chemical transformation is not straightforward. Here, we demonstrate that extrinsic force exerted upon cyclobutanes by stretching pendant polymer chains influences product selectivity through force-imparted nonstatistical dynamic effects on the stepwise ring-opening reaction. The high product stereoselectivity is quantified by carbon-13 labeling and shown to depend on external force, reactant stereochemistry, and intermediate stability. Computational modeling and simulations show that, besides altering energy barriers, the mechanical force activates reactive intramolecular motions nonstatistically, setting up “flyby trajectories” that advance directly to product without isomerization excursions. A mechanistic model incorporating nonstatistical dynamic effects accounts for isomer-dependent mechanochemical stereoselectivity. 

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2. Mechanochemical Reactivity of a Multimodal 2H-Bis-Naphthopyran Mechanophore

   https://doi.org/10.1039/d3py00344b  

   Osler, Skylar K.; McFadden, Molly E.; Zeng, Tian; Robb, Maxwell J. (June 2023, Polymer Chemistry)

   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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3. Allosteric control of olefin isomerization kinetics via remote metal binding and its mechanochemical analysis

   https://doi.org/10.1038/s41467-023-40842-5  

   Yu, Yichen; O’Neill, Robert T.; Boulatov, Roman; Widenhoefer, Ross A.; Craig, Stephen L. (December 2023, Nature Communications)

   Abstract Allosteric control of reaction thermodynamics is well understood, but the mechanisms by which changes in local geometries of receptor sites lower activation reaction barriers in electronically uncoupled, remote reaction moieties remain relatively unexplored. Here we report a molecular scaffold in which the rate of thermal E-to-Z isomerization of an alkene increases by a factor of as much as 10 4 in response to fast binding of a metal ion to a remote receptor site. A mechanochemical model of the olefin coupled to a compressive harmonic spring reproduces the observed acceleration quantitatively, adding the studied isomerization to the very few reactions demonstrated to be sensitive to extrinsic compressive force. The work validates experimentally the generalization of mechanochemical kinetics to compressive loads and demonstrates that the formalism of force-coupled reactivity offers a productive framework for the quantitative analysis of the molecular basis of allosteric control of reaction kinetics. Important differences in the effects of compressive vs. tensile force on the kinetic stabilities of molecules are discussed. 

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4. Force Transduction Through Distant Force‐Bearing Regioisomeric Linkages Affects the Mechanochemical Reactivity of Cyclobutane

   https://doi.org/10.1002/anie.202406103  

   Flear, Erica J; Horst, Maggie; Yang, Jinghui; Xia, Yan (August 2024, Angewandte Chemie International Edition)

   Fundamental understanding of mechanochemical reactivity is important for designing new mechanophores. Besides the core structure of mechanophores, substituents on a mechanophore can affect its mechanochemical reactivity through electronic stabilization of the intermediate or effectiveness of force transduction from the polymer backbone to the mechanophore. The latter factor represents a unique mechanical effect in considering polymer mechanochemistry. Here, we show that regioisomeric linkage that is not directly adjacent to the first cleaving bond in cyclobutane can still significantly affect the mechanochemical reactivity of the mechanophore. We synthesized three non‐scissile 1,2‐diphenyl cyclobutanes, varying their linkage to the polymer backbone via theo,m, orp‐position of the diphenyl substituents. Even though the regioisomers share the same substituted cyclobutane core structure and similar electronic stabilization of the diradical intermediate from cleaving the first C−C bond, thepisomer exhibited significantly higher mechanochemical reactivity than theoandmisomers. The observed difference in reactivity can be rationalized as the much more effective force transduction to the scissile bond through thep‐position than the other two substitution positions. These findings point to the importance of considering force‐bearing linkages that are more distant from the bond to be cleaved when incorporating mechanophores into polymer backbones. 

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5. The tension-activated carbon–carbon bond

   https://doi.org/10.1016/j.chempr.2024.05.012  

   Sun, Yunyan; Kevlishvili, Ilia; Kouznetsova, Tatiana B; Burke, Zach P; Craig, Stephen L; Kulik, Heather J; Moore, Jeffrey S (June 2024, Chem)

   Mechanical force drives distinct chemical reactions; yet, its vectoral nature results in complicated coupling with reaction trajectories. Here, we utilize a physical organic model inspired by the classical Morse potential and its differential forms to identify effective force constant (keff) and reaction energy (ΔE) as key molecular features that govern mechanochemical kinetics. Through a comprehensive experimental and computational investigation with four norborn-2-en-7-one (NEO) mechanophores, we establish the relationship between these features and the force-dependent energetic changes along the reaction pathways. We show that the complex kinetic behavior of the tensioned bonds is generally and quantitatively predicted by a simple multivariate linear regression based on the two easily computed features with a straightforward workflow. These results demonstrate a general mechanistic framework for mechanochemical reactions under tensile force and provide a highly accessible tool for the large-scale computational screening in the design of mechanophores. 

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