Quantification of the H-Bond-Donating Ability of Trifluoromethyl Ketone Hydrates Using a Colorimetric Sensor
Trifluoromethyl ketones (TFMKs) readily form stable hydrates and hemiketals in solution, allowing them to interact with biomolecules as hydrogen-bond donors. This interaction is governed by both the hydration equilibrium and the intrinsic hydrogen-bonding strength for a given compound. The hydrogen-bond-donating abilities for aryl, heterocyclic, and alkyl TFMKs were experimentally determined by using UV-vis titrations with a colorimetric sensor. Values were also adjusted based on the percent hydrate present in solution to provide insight into the hydrogen-bond-donating ability of the hydrate species.
Authors
- Cameron B. Berlin (ORCID: https://orcid.org/0009-0002-7742-2722)
- Marisa C. Kozlowski (ORCID: https://orcid.org/0000-0002-4225-7125)
- C Zheng
- Emily Sidlow
Institutions
- California University of Pennsylvania (US)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-05-15
- DOI
- https://doi.org/10.1021/acs.joc.4c03046
- Citations
- 1
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.79
Funders
- National Institute of General Medical Sciences