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

Yichen Yu, Robert T. O’Neill, Roman Boulatov (), Ross A. Widenhoefer () and Stephen L. Craig ()
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Yichen Yu: Duke University
Robert T. O’Neill: University of Liverpool
Roman Boulatov: University of Liverpool
Ross A. Widenhoefer: Duke University
Stephen L. Craig: Duke University

Nature Communications, 2023, vol. 14, issue 1, 1-10

Abstract: 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 104 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.

Date: 2023
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DOI: 10.1038/s41467-023-40842-5

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