Macromolecular architecture plays a pivotal role in determining the properties of polymers. When designing polymers for specific applications, it is not only the size of a macromolecule that must be considered, but also its shape. In most cases, the topology of a polymer is a static feature that is inalterable once synthesized. Using reversible-covalent chemistry to prompt the disconnection of chemical bonds and the formation of new linkages in situ, we report polymers that undergo dramatic topological transformations via a process we term macromolecular metamorphosis. Utilizing this technique, a linear amphiphilic block copolymer or hyperbranched polymer undergoes 'metamorphosis' into comb, star and hydrophobic block copolymer architectures. This approach was extended to include a macroscopic gel which transitioned from a densely and covalently crosslinked network to one with larger distances between the covalent crosslinks when heated. These architectural transformations present an entirely new approach to 'smart' materials.
Traditional shape memory polymers (SMPs) are mostly thermoresponsive, and their applications in nano-optics are hindered by heat-demanding programming and recovery processes. By integrating a polyurethane-based shape memory copolymer with templating nanofabrication, reconfigurable/rewritable macroporous photonic crystals have been demonstrated. This SMP coupled with the unique macroporous structure enables unusual all-room-temperature shape memory cycles. "Cold" programming involving microscopic order-disorder transitions of the templated macropores is achieved by mechanically deforming the macroporous SMP membranes. The rapid recovery of the permanent, highly ordered photonic crystal structure from the temporary, disordered configuration can be triggered by multiple stimuli including a large variety of vapors and solvents, heat, and microwave radiation. Importantly, the striking chromogenic effects associated with these athermal and thermal processes render a sensitive and noninvasive optical methodology for quantitatively characterizing the intriguing nanoscopic shape memory effects. Some critical parameters/mechanisms that could significantly affect the final performance of SMP-based reconfigurable photonic crystals including strain recovery ratio, dynamics and reversibility of shape recovery, as well as capillary condensation of vapors in macropores, which play a crucial role in vapor-triggered recovery, can be evaluated using this new optical technology.
This study reports unconventional, all-room-temperature shape memory (SM) effects using templated macroporous shape memory polymer (SMP) photonic crystals comprising a glassy copolymer with high-glass transition temperature. "Cold" programming of permanent periodic structures into temporary disordered configurations can be achieved by slowly evaporating various swelling solvents (e.g., ethanol) imbibed in the interconnecting macropores. The deformed macropores can be instantaneously recovered to the permanent geometry by exposing it to vapors and liquids of swelling solvents. By contrast, nonswelling solvents (e.g., hexane) cannot trigger "cold" programming and SM recovery. Extensive experimental and theoretical investigations reveal that the dynamics of swelling-induced plasticizing effects caused by fast diffusion of solvent molecules into the walls of macropores with nanoscopic thickness dominate both "cold" programming and recovery processes. Importantly, the striking color changes associated with the reversible SM transitions enable novel chromogenic sensors for selectively detecting trace amounts of swelling analytes mixed in nonswelling solvents. Using ethanol-hexane solutions as proof-of-concept mixtures, the ethanol detection limit of 150 ppm has been demonstrated. Besides reusable sensors, which can find important applications in environmental monitoring and petroleum process/product control, the programmable SMP photonic crystals possessing high mechanical strengths and all-room-temperature processability can provide vast opportunities in developing reconfigurable/rewritable nanooptical devices.
Two sets of reversible covalent linkages distributed in series along a polymer backbone were used to prepare a new class of doubly dynamic-covalent polymers capable of reversibly dissociating via two distinct pathways.
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