Research Overview and Links
The unifying theme in my research lab is organic synthesis, but our research projects have been highly varied.
One project we've worked on involves the synthesis of molecules that are structurally modified versions of the well known antioxidant Vitamin E, in hopes that these new molecules will target mitochondria in cells (which is where the majority of oxidative damage occurs). This would prove useful in combating diseases such as Alzheimer's, Parkinson's, Lou Gehrig's, and various cancers.
Several students have also worked with reactive molecules known as stable silylenes and have explored the application of these compounds as catalysts in new organometallic reactions. Stable silylenes are excellent metal ligands and have shown to act as phenomenal catalysts (similar to phosphines) in certain organic reactions. The Stille reaction, for example, can employ palladium-silylene complexes to create new C-C bonds between molecules. Our research is involved with designing, testing, and observing the mechanisms of such catalysts.
Microfluidics has proven to show great promise in the world of synthetic chemistry, and the third area of our research deals with developing and refining new techniques in this field. Moving beyond the standard "reaction pot" methods, microfluidics involves a mobile liquid phase (dissolved or pure reagent) which flows through a tiny reaction chamber. A second reagent is injected directly into the mobile phase chamber (much like a stream would flow into a river), creating thousands of tiny, isolated reactions. The product is then collected as the mobile phase carries it to the end of the reaction vessel.
We are continuing to study an interesting organic reaction that affords tertiary amines from alkyl nitriles under palladium catalyzed reducing conditions. The outcome of these reactions can change depending on the solvent choice, and afford products in nearly quantitative yields.
One of our newest projects deals with the synthesis of organometallic catalysts designed to make biodegradable polymers from non-petroleum resources. Specifically, we are exploring the ring-opening polymerization (ROP) of lactide to polylactic acid (PLA) via the use of aluminum based catalysts. Because lactide monomer can be produced via the fermentation of corn or sugar beets, the polymerization of lactide to PLA represents a carbon-neutral process. As such, this polymer has been the subject of high interest, and it is already manufactured in large quantitites for use in applications such as absorbable sutures, biodegradable flatware, and packaging material. ROP is a useful route to study, as it affords careful control over the polymers physical and chemical properties. This work is being done in collaboration with Professor Charlotte Williams at Imperial College in London.