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Mechanoactivated amorphization and photopolymerization of styryldipyryliums.
Usuba, Junichi; Sun, Zhenhuan; Nguyen, Han P Q; Raju, Cijil; Schmidt-Rohr, Klaus; Han, Grace G D.
  • Usuba J; Department of Chemistry, Brandeis University, 415 South Street, Waltham, MA 02453 USA.
  • Sun Z; Department of Chemistry, Brandeis University, 415 South Street, Waltham, MA 02453 USA.
  • Nguyen HPQ; Department of Chemistry, Brandeis University, 415 South Street, Waltham, MA 02453 USA.
  • Raju C; Department of Chemistry, Brandeis University, 415 South Street, Waltham, MA 02453 USA.
  • Schmidt-Rohr K; Department of Chemistry, Brandeis University, 415 South Street, Waltham, MA 02453 USA.
  • Han GGD; Department of Chemistry, Brandeis University, 415 South Street, Waltham, MA 02453 USA.
Commun Mater ; 5(1): 98, 2024.
Article en En | MEDLINE | ID: mdl-38859933
ABSTRACT
Conventional 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.
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