Photolabile polymer materials have attracted considerable scientific and societal attention owing to the spatiotemporal control of light. However, easily photoreactive polymers are intrinsically unstable, leading to a tradeoff between their reactivity and stability. This article reports a proof-of-concept for reversible switching between photostable and photolabile states in polymer network materials enabled by the supramolecular transformation of the kinetically stable pseudo[1]rotaxane.
View Article and Find Full Text PDFMaterial photocontrol has gained importance in process engineering and biomedical applications. However, highly photoreactive materials are intrinsically unstable to light, which limits their continuous use in lit environments owing to their gradual deterioration. Herein, synergistically photocontrollable materials in the presence of acid are developed to overcome the conventional trade-off between their photoreactivity and photostability.
View Article and Find Full Text PDFPolyacrylate-based network materials are widely used in various products owing to their facile synthesis via radical polymerization reactions. In this study, the effects of alkyl ester chains on the toughness of polyacrylate-based network materials were investigated. Polymer networks were fabricated via the radical polymerization of methyl acrylate (MA), ethyl acrylate (EA), and butyl acrylate (BA) in the presence of 1,4-butanediol diacrylate as a crosslinker.
View Article and Find Full Text PDFPhotopolymerization and photoprocessing are core technologies for molding and tuning polymer materials. However, they are incompatible with single materials owing to their contradictory photoreactivity. Herein, an acid-induced photocleavable crosslinker, a platinum-acetylide complex covered by permethylated cyclodextrins, enables the fabrication of photoprocessable materials via photopolymerization with N-(2-hydroxyethyl)acrylamide.
View Article and Find Full Text PDF