Abstract
AbstractConventional topochemical photopolymerization reactions occur exclusively in precisely-engineered photoactive crystalline states, which often produces high-insoluble polymers. To mitigate this, here, we report the mechanoactivation of photostable styryldipyrylium-based monomers, which results in their amorphization-enabled solid-state photopolymerization and produces soluble and processable amorphous polymers. A combination of solid-state nuclear magnetic resonance, X-ray diffraction, and absorption/fluorescence spectroscopy reveals the crucial role of a mechanically-disordered monomer phase in yielding polymers via photo-induced [2 + 2] cycloaddition reaction. Hence, mechanoactivation and amorphization can expand the scope of topochemical polymerization conditions to open up opportunities for generating polymers that are otherwise difficult to synthesize and analyze.
Funder
United States Department of Defense | United States Air Force | AFMC | Air Force Office of Scientific Research
NSF | Directorate for Mathematical & Physical Sciences | Division of Materials Research
Alfred P. Sloan Foundation
Camille and Henry Dreyfus Foundation
NSF | Directorate for Mathematical & Physical Sciences | Division of Chemistry
U.S. Department of Health & Human Services | National Institutes of Health
Publisher
Springer Science and Business Media LLC