Harnessing light to drive a non-photoresponsive reaction out of equilibrium

<h2>Summary</h2> Driving non-photoresponsive transformations out of equilibrium with light requires transducing light energy into a different stimulus. Here, we demonstrate this using a dynamic-covalent network of four interconverting imines. In this system, photoirradiation drives a transimination reaction involving photoswitchable imines into a non-equilibrium steady state, altering the composition of both the photochromic imines and free amines. This shift in amine composition subsequently perturbs a coupled transimination reaction that does not directly absorb this wavelength of light. Notably, coupling these two reactions enhances the system's response; the amines generated in each transimination facilitate the other, amplifying the overall departure from equilibrium beyond what is observed for the reactions in isolation. Operating entirely in solution, this light-fueled cascade provides a blueprint for designing dynamic-covalent systems that harness light energy to control non-photoresponsive transformations, expanding the scope and complexity of light-driven processes in systems chemistry.

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Publication Details

Journal
Chem
Published
2025-05-05
DOI
https://doi.org/10.1016/j.chempr.2025.102579
Citations
9
Primary Topic
Photoreceptor and optogenetics research
Type
article
Field-Weighted Citation Impact
8.18

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article

Harnessing light to drive a non-photoresponsive reaction out of equilibrium

Jake L. Greenfield, Jiarong Wu
9 citations
Chem
Photoreceptor and optogenetics research
8.18
article

Harnessing light to drive a non-photoresponsive reaction out of equilibrium

Jake L. Greenfield, Jiarong Wu
article en
9 citations

Abstract

<h2>Summary</h2> Driving non-photoresponsive transformations out of equilibrium with light requires transducing light energy into a different stimulus. Here, we demonstrate this using a dynamic-covalent network of four interconverting imines. In this system, photoirradiation drives a transimination reaction involving photoswitchable imines into a non-equilibrium steady state, altering the composition of both the photochromic imines and free amines. This shift in amine composition subsequently perturbs a coupled transimination reaction that does not directly absorb this wavelength of light. Notably, coupling these two reactions enhances the system's response; the amines generated in each transimination facilitate the other, amplifying the overall departure from equilibrium beyond what is observed for the reactions in isolation. Operating entirely in solution, this light-fueled cascade provides a blueprint for designing dynamic-covalent systems that harness light energy to control non-photoresponsive transformations, expanding the scope and complexity of light-driven processes in systems chemistry.

ChemVol. 11(10)
University of Würzburg (DE)
Verband der Chemischen Industrie, Fonds der Chemischen Industrie
Climate action
Openalex Percentile: Top 2%
Photoreceptor and optogenetics research
8.18
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