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Rapid Synthesis of Naphthol Derivatives through a Photocontrolled Exothermic Process

Organic Letters

Xu, Zhenchuang; Bean, Ren H.; Hausladen, Matthew M.; Leguizamon, Samuel C.; Moore, Jeffrey S.; Appelhans, Leah N.

A photocontrolled isomerization reaction of oxabenzonorbornadiene (OBNBD) derivatives with a photo acid generator (PAG) has been developed. Under irradiation, the PAG releases an acid that catalyzes the heterolytic cleavage of the benzyl ether, triggering an aromatization process accompanied by substantial heat release that accelerates the transformation. Large exotherms can further push low reactivity substrates to achieve full conversion within minutes. This approach not only illuminates practical and environmentally benign advantages in organic synthesis but also opens new avenues for developing photoresponsive molecular architectures and advanced functional materials.

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Active light-controlled frontal ring-opening metathesis polymerization

Nature Communications

Appelhans, Leah N.; Darby, Daniel R.; Greenlee, Andrew J.; Bean, Ren H.; Fairchild, David C.; Rodriguez, Victoria C.; Jansen, Annika L.; Gallegos, Shantae C.; Ramirez, Salma P.; Leguizamon, Samuel C.

Frontal ring-opening metathesis polymerization (FROMP) is a promising energy-efficient approach to fabricate polymeric materials. Recent advances have demonstrated FROMP for diverse applications, including additive manufacturing, composites, and foams. However, the characteristic properties of the front are currently controlled primarily by varying the resin composition or the environmental conditions. In this work we present an approach to control FROMP of dicyclopentadiene (DCPD) using photochemical methods. A photobase generator is used to inhibit FROMP of DCPD with UV light while a photosensitizer and co-initiator are used to accelerate FROMP with blue light, enabling orthogonal active photocontrol of front velocity. In addition, photoinhibition-enabled lithographic patterning of frontal polymerizations is demonstrated. Frontal polymerizations are spatially controlled, redirected, and even split into diverging fronts. This work establishes a foundation for advanced control of frontal polymerizations, enabling innovation in traditional and additive manufacturing, as well as emerging processes like morphogenic manufacturing.

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Advances in vat photopolymerization: early-career researchers shine light on a path forward

RSC Applied Polymers

Fowler, Hayden E.; Bean, Ren H.; Dhand, Abhishek P.; Saccone, Max A.; Chiaradia, Viviane; Dranseike, Dalia; Fraser, Julia M.; Howard, Holden; Kaneko, Takashi; Kim, Ji W.; Kronenfeld, Jason M.; Mason, Keldy S.; O'Dea, Connor J.; Pashley-Johnson, Fred; Porcincula, Dominique H.; Segal, Maddison I.; Yu, Siwei

Vat photopolymerization (VP) has emerged as a promising additive manufacturing technique to allow rapid light-based fabrication of 3D objects from a liquid resin. Research in the field of vat photopolymerization spans across multiple disciplines from engineering and materials science to applied chemistry and physics. This perspective brings together early-career researchers from various disciplines in academia and national laboratories around the world to summarize the most recent advancements with special emphasis on the research highlighted as part of the Gordon Research Conference (GRC) 2024 meeting on Additive Manufacturing of Soft Materials. We provide an outlook on next-generation polymer processing methods from synthesis of novel materials to multimodality manufacturing and performance engineering. Further, this article combines the ideas of many of these junior researchers to present a vision for the future of the field by highlighting the challenges and opportunities that lie ahead.

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