Hydroxymethylated Quinones for CO₂ Capture
Electrochemical CO₂ capture using quinones is a promising alternative to energy-intensive amine scrubbing. However, the negative redox potentials needed to generate strongly nucleophilic dianions also increase oxygen sensitivity. My research tries to solve this problem by introducing a covalently linked H-bonding arm connected through a flexible benzylic C–C bond to the quinone scaffold. Upon two-electron reduction, this arm rotates to position the hydroxymethyl group to stabilize the dianion via H-bonding, circumventing the fundamental linear trade-off that has constrained quinone-based capture systems.

- Synthesized and characterized 6+ hydroxymethylated quinone (HMQ) derivatives.
- Spectroscopic/electrochemical confirmation of aryl-carbonate adducts.
- Independent control over reduction potential and binding affinity.

