Pre‐Activation as a Route for Tuning the Kinetics of Mechanochemical Transformations

Learning to control reaction kinetics is essential for translating any chemical technology into real-world application. Based on time-resolved in situ powder X-ray diffraction data, we demonstrate the opportunity to tune mechanochemical reaction rates through the pre-activation of the starting reagents. For three model co-crystal systems, the pre-activation of the most stable reagent yields up to a ca 10-fold increase in the reaction rate, whilst negligible kinetic enhancement is seen when the less stable reagent is pre-activated. Moreover, we demonstrate how the polymorphic outcome of mechano-co-crystallization is also sensitive to pre-activation of the starting material. Our results suggest that reproducibility of mechanochemical processes requires detailed understanding over the origin and history of reagent powders, whilst providing a new conceptual framework to design and control mechanochemical reactions.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-11-23
DOI
https://doi.org/10.1002/anie.202516632
Primary Topic
Crystallography and molecular interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Pre‐Activation as a Route for Tuning the Kinetics of Mechanochemical Transformations

Christian Heinekamp, Andrew F. May, Š. Michalik, Carsten Prinz et al.
Angewandte Chemie International Edition
Crystallography and molecular interactions
article

Pre‐Activation as a Route for Tuning the Kinetics of Mechanochemical Transformations

Christian Heinekamp, Andrew F. May, Š. Michalik, Carsten Prinz, Dominik Al‐Sabbagh, Franziska Emmerling, Tracy Palmer, Adam A. L. Michalchuk∞
article en

Abstract

Learning to control reaction kinetics is essential for translating any chemical technology into real-world application. Based on time-resolved in situ powder X-ray diffraction data, we demonstrate the opportunity to tune mechanochemical reaction rates through the pre-activation of the starting reagents. For three model co-crystal systems, the pre-activation of the most stable reagent yields up to a ca 10-fold increase in the reaction rate, whilst negligible kinetic enhancement is seen when the less stable reagent is pre-activated. Moreover, we demonstrate how the polymorphic outcome of mechano-co-crystallization is also sensitive to pre-activation of the starting material. Our results suggest that reproducibility of mechanochemical processes requires detailed understanding over the origin and history of reagent powders, whilst providing a new conceptual framework to design and control mechanochemical reactions.

Angewandte Chemie International EditionVol. 65(3)
Federal Institute For Materials Research and Testing (DE), Diamond Light Source (GB), Humboldt-Universität zu Berlin (DE), Zero to Three (US), University of Birmingham (GB)
Diamond Light Source, Deutsche Forschungsgemeinschaft, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 68%
Crystallography and molecular interactions
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Pre‐Activation as a Route for Tuning the Kinetics of Mechanochemical Transformations — Christian Heinekamp, Andrew F. May, et al. · Angewandte Chemie International Edition (2025) | TGRS Research Map | TGRS