材料科学
聚合物
高分子科学
结构着色
纳米技术
复合材料
光电子学
光子晶体
作者
Arnau Marco,Marc Villabona,Tugce Nur Eren,Florian Feist,Gonzalo Guirado,Rosa Marı́a Sebastián,Jordi Hernando,Christopher Barner‐Kowollik
标识
DOI:10.1002/adfm.202415431
摘要
Abstract Offering high spatiotemporal resolution, dual wavelength‐controlled soft matter network formation paves the way to advanced printing techniques with optimized performance. One of the most promising approaches is the antagonistic control of covalent bond‐forming reactions with two colors of light, where photoexcitation with one wavelength induces a photochemical reaction, while irradiation with the other ceases it in the presence of the first color. Herein, we combine a photoactivatable diene precursor and a photoswitchable dienophile, establishing a dual‐wavelength‐gated cycloaddition reaction capable of controlling polymer crosslinking. Upon incorporation of the diene precursor into a methacrylate copolymer and the synthesis of a difunctional dienophile cross‐linker, selective polymer network formation is promoted under sole UV illumination, while it can be efficiently suppressed with simultaneous redlight irradiation. Critically, the methodology is used for the preparation of solid polymer materials with antagonistic two‐color control of their cross‐linking status, ultimately allowing the fabrication of spatially patterned polymer films.
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