Utilizing Similarity Measures to Map Chemical Reactivity

The development of fully autonomous chemical synthesis platforms requires robust, real-time assessment of reactivity that does not rely on prior mechanistic knowledge. Existing methods often depend on predefined reaction models or chemical intuition, limiting their generalizability and adaptability. To address this challenge, we introduce a chemically agnostic approach that quantifies reactivity dynamics by applying similarity metrics to the full informational content of in-situ spectroscopic data. Using NMR, UV/Vis, IR, and EPR spectroscopy, we demonstrate that spectral similarity trajectories can reliably indicate reaction progress, detect kinetic features such as autocatalysis, and resolve complex behaviours including oscillations. Across diverse reaction classes, this method enabled estimated end-point detection and kinetic profiling without reaction-specific tuning. For example, the formation of lophine was followed by NMR at different reaction temperatures revealing Arrhenius-type kinetics. In a different experiment, the Belousov Zhabotinsky reaction was monitored by UV/Vis and the chemical oscillation with a periodicity of 7.25 s was captured. These results establish a generalizable framework for real-time, data-driven reactivity monitoring, representing a critical step toward autonomous synthesis guided by multidimensional spectroscopic feedback.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-11-20
DOI
https://doi.org/10.1002/anie.202521519
Citations
1
Primary Topic
Molecular spectroscopy and chirality
Type
article
Field-Weighted Citation Impact
0.76

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article

Utilizing Similarity Measures to Map Chemical Reactivity

Robert Rauschen, Leroy Cronin, Dean Thomas
1 citations
Angewandte Chemie International Edition
Molecular spectroscopy and chirality
0.76
article

Utilizing Similarity Measures to Map Chemical Reactivity

Robert Rauschen, Leroy Cronin, Dean Thomas
article en
1 citations

Abstract

The development of fully autonomous chemical synthesis platforms requires robust, real-time assessment of reactivity that does not rely on prior mechanistic knowledge. Existing methods often depend on predefined reaction models or chemical intuition, limiting their generalizability and adaptability. To address this challenge, we introduce a chemically agnostic approach that quantifies reactivity dynamics by applying similarity metrics to the full informational content of in-situ spectroscopic data. Using NMR, UV/Vis, IR, and EPR spectroscopy, we demonstrate that spectral similarity trajectories can reliably indicate reaction progress, detect kinetic features such as autocatalysis, and resolve complex behaviours including oscillations. Across diverse reaction classes, this method enabled estimated end-point detection and kinetic profiling without reaction-specific tuning. For example, the formation of lophine was followed by NMR at different reaction temperatures revealing Arrhenius-type kinetics. In a different experiment, the Belousov Zhabotinsky reaction was monitored by UV/Vis and the chemical oscillation with a periodicity of 7.25 s was captured. These results establish a generalizable framework for real-time, data-driven reactivity monitoring, representing a critical step toward autonomous synthesis guided by multidimensional spectroscopic feedback.

Angewandte Chemie International EditionVol. 65(2)
University of Glasgow (GB)
Bill and Melinda Gates Foundation, University of Glasgow, National Institutes of Health, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 23%
Molecular spectroscopy and chirality
0.76
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