Our group is dedicated to elucidating the intricacies of molecular structure and reactivity, drawing upon advanced theoretical and experimental methodologies within the field of Physical Organic Chemistry. This area, marked by its intellectual rigor and imaginative exploration, often compels us to reconsider prevailing notions about chemical reactions and molecular properties. In particular, we are engrossed in a comprehensive study of the physicochemical properties of organofluorine compounds. We aim to discern the ramifications of both classical effects and quantum stereoelectronic effects on the structure and reactivity of these unique molecular systems. We also employ state-of-art experimental and computational chemistry techniques to dissect fundamental organic reactions and reveal nuanced facets of their underlying mechanisms.
Consequently, our research methodology cohesively integrates both theoretical and experimental techniques to elucidate the physicochemical properties and reactivity patterns of organic molecules. The incorporation of fluorine frequently imparts unique properties to these molecules, thereby positing complex challenges to current theoretical and experimental approaches. Such challenges become prominently evident when endeavoring to elucidate molecular structure and reactivity mechanisms of fluorinated organic molecules. Our comprehensive approach spans spectroscopic techniques and detailed mechanism investigations, further fortified by computational calculations and theory. In a succinct yet somewhat reductive overview, our research methodologies can be characterized as
1 – Physical organic chemistry: Physicochemical studies of organofluorine compounds.
2 – Structure, conformation and stereochemistry of organic molecules.
3 – Applications of theoretical chemistry, NMR and infrared spectroscopies on organic compounds.
4 – Mechanistic studies of organic reactions using experimental and theoretical approaches.
For a deeper insight into our research, take a look at published papers on the Publications page.