Dissecting Binary and Ternary Iminoboronate Assemblies: A Calorimetric Study of Thermodynamics, Kinetics, and Allosteric Effects
Dynamic covalent assemblies derived from ortho-boronoaldehydes, including iminoboronates and boronate esters, are key structural motifs in adaptive materials, chemical sensors, and reversible bioconjugation strategies. Herein, we report a label-free assay based on isothermal titration calorimetry that provides access to observed thermodynamic and model-derived kinetic parameters associated with assembly formation under defined experimental conditions. The assay further reveals cooperative binding between amine-based nucleophiles and diols toward ortho-boronoaldehyde derivatives, providing new insight into multicomponent dynamic covalent systems.
Authors
- Eduardo Laga (ORCID: https://orcid.org/0000-0003-1882-2558)
- Joseba Ruiz (ORCID: https://orcid.org/0009-0009-5056-5134)
- Jesús del Barrio (ORCID: https://orcid.org/0000-0002-5380-6863)
- Adrián Velázquez‐Campoy (ORCID: https://orcid.org/0000-0001-5702-4538)
Institutions
- Universidad de Zaragoza (ES)
- Instituto de Nanociencia y Materiales de Aragón (ES)
- Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (ES)
- Instituto de Investigación Sanitaria Aragón (ES)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-10-14
- DOI
- https://doi.org/10.1021/acs.joc.6c01363
- Primary Topic
- Supramolecular Chemistry and Complexes
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- European Commission
- Universidad de Zaragoza
- Agencia Estatal de Investigación
- NextGenerationEU