Encapsulated Transition Metal Catalysts Enable Long-term Stability in Frontal Polymerization Resins

• Published in: Macromolecules Vol. 56; no. 18; pp. 7543 - 7550
• Main Authors: Davydovich, Oleg, Greenlee, Andrew J., Root, Harrison D., Jansen, Annika L., Gallegos, Shantae C., Warner, Matthew J., Kent, Michael S., Cardenas, Jorge A., Appelhans, Leah N., Roach, Devin J., Jones, Brad H., Leguizamon, Samuel C.
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 26-09-2023
• Subjects: encapsulation; frontal polymerization; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; pot life; ring-opening metathesis polymerization; thermosets
• ISSN: 0024-9297; 1520-5835
• DOI: 10.1021/acs.macromol.3c01146

Frontal polymerization involves the propagation of a thermally driven polymerization wave through a monomer solution to rapidly generate high-performance polymeric materials with little energy input. The balance between latent catalyst activation and sufficient reactivity to sustain a front can be difficult to achieve and often results in systems with poor storage lives. This is of particular concern for frontal ring-opening metathesis polymerization (FROMP) where gelation occurs within a single day of resin preparation due to the highly reactive nature of Grubbs-type catalysts. Here, we demonstrate the use of encapsulated catalysts to provide remarkable latency to frontal polymerization systems, specifically using the highly active dicyclopentadiene monomer system. Negligible differences were observed in the frontal velocities or thermomechanical properties of the resulting polymeric materials. FROMP systems with encapsulated catalyst particles are shown with storage lives exceeding 12 months and front rates that increase over a well-characterized 2 month period. Moreover, the modularity of this encapsulation method is demonstrated by encapsulating a platinum catalyst for the frontal polymerization of silicones by using hydrosilylation chemistry.