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.
Authors
- Christian Heinekamp (ORCID: https://orcid.org/0000-0003-4306-2909)
- Andrew F. May (ORCID: https://orcid.org/0000-0003-0777-8539)
- Š. Michalik (ORCID: https://orcid.org/0000-0001-9459-322X)
- Carsten Prinz (ORCID: https://orcid.org/0000-0001-8586-5430)
- Dominik Al‐Sabbagh (ORCID: https://orcid.org/0000-0001-7203-8903)
- Franziska Emmerling (ORCID: https://orcid.org/0000-0001-8528-0301)
- Tracy Palmer (ORCID: https://orcid.org/0000-0001-9043-2592)
- Adam A. L. Michalchuk∞ (ORCID: https://orcid.org/0000-0001-7405-3269)
Institutions
- 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)
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
Funders
- Diamond Light Source
- Deutsche Forschungsgemeinschaft
- Engineering and Physical Sciences Research Council