Active Cells, Biochemistry & Physiology Chemistry

Polymer Mechanochemistry Enhanced with Mechanically Interlocked Molecules

In plain English

AI plain-English summary

A polymer chain can be made to "grab" a chemical group without being permanently attached to it, using a molecular ring threaded on an axle—a rotaxane—to repeatedly pull bonds apart and build new molecules. This matters because mechanical force can drive chemical reactions that heat or light cannot, but current methods only work once: the polymer must be covalently bonded to the mechanophore, and the bond breaks irreversibly. The rotaxane architecture solves that by letting the polymer slide along the axle, grip the mechanophore, release it, and repeat the action—something impossible with fixed attachments. If successful, this would unlock repetitive mechanochemical reactions and even force-driven molecular assembly. That could transform how we manufacture materials that respond to stress, such as self-healing plastics, force-sensing coatings, or polymers that change colour under load. These applications matter for infrastructure, automotive components, and protective gear—systems where detecting or repairing damage automatically could extend lifetimes and reduce waste. The project is fundamental science: it explores a new principle of how mechanical energy can be transduced at the molecular level. Past work on interlocked molecules already gave us molecular switches and motors; this could add a new tool for building and breaking bonds on demand.

View original technical description
Mechanical force is a formidable source of energy that, with its ability to distort, bend and stretch chemical bonds, is unique in the way it activates chemical reactions. In polymer mechanochemistry, polymers are used to transduce mechanical force towards a mechanoresponsive functional group (a "mechanophore") that then undergoes a mechanochemical transformation. Although mechanical force is exceptional in its ability to promote reaction pathways that are otherwise inaccessible, it has so far been limited to transformations involving bond cleavage or rearrangements. The origin of these limitations is due to the fact that the actuating polymers have to be linked to the mechanophore to activate it, which has so far made impossible to: repetitively activate scissile mechanophores or to build molecules. A solution to that problem would be to find a way for the polymer to 'grab' the mechanophore without being covalently attached to it. Interlocked molecules, which have been instrumental in the development of molecular machines, are ideally suited for that task because their subcomponents are entangled in space but not covalently linked. As a result, they can undergo large amplitude internal displacements, such as a macrocycle shuttling along the axle of a rotaxane, which makes them attractive force actuators. In this programme, we want to demonstrate how a rotaxane architecture can be used to repetitively activate scissile mechanophores and to build molecules.

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Researchers

Guillaume De Bo (Principal Investigator)

Related Research

Grants with similar aims, by meaning.

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Dynamic Mechanically Interlocked Rotaxane and Catenane Catalysts for Isoselective Ring Opening Polymerisation
Chemically fuelled autonomous directional linear motion at the molecular level
Chemomechanics: a bridge across the formidable gap
Molecular Machines with Integrated Parts

Original classification

Research Grant

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