Supramolecular structures are formed through the assembly of individual molecules via non-covalent interactions, yielding unique architectures with diverse applications. Our group synthesizes molecular building blocks that are rationally designed to self-assemble into higher-order structures, whose physical and chemical properties are subsequently investigated.  

Our group is interested in understanding and controlling light–matter interactions in functional organic materials. Through the rational design and synthesis of phosphorescent three-dimensional (3D) covalent organic frameworks (COFs), we investigate how structural rigidity, porosity, and molecular organization influence their photophysical properties. These emerging materials exhibit unique luminescent behavior and show promise for applications in sensing, optoelectronics, and oxygen detection.

Our group finds beauty in the diverse architectcures accessible through modern day organic synthesis, but we are also interested in the functionality of these structures. Materials formed by organic building blocks have demonstrated properties from sensing to semiconducting, making them attractive for the creation of flexible electronics. 

How do small changes at the molecular level affect the assembly of crystal structures, and how can chemical intuition be leveraged to induce desired structural changes? These questions guide the research in our group at a fundamental level. Maybe more...?

Commonly referred to as molecular sponges, porous materials are a rising class of molecular assemblies with applications in gas adsorption, catalysis, and membrane technologies. Our group synthesizes covalent organic frameworks (COFs) and organic cages and characterizes them through techniques such as X-ray diffraction and porosimetry.