Acoustodynamic Covalent Materials Engineering for the Remote Control of Physical Properties Inside Materials

Abstract

AbstractAdvances in vat photopolymerization (VP) 3D printing (3DP) technology enable the production of highly precise 3D objects. However, it is a major challenge to create dynamic functionalities and to manipulate the physical properties of the inherently insoluble and infusible cross‐linked material generated from VP‐3DP without reproduction. The fabrication of light‐ and high‐intensity focused ultrasound (HIFU)‐responsive cross‐linked polymeric materials linked with hexaarylbiimidazole (HABI) in polymer chains based on VP‐3DP is reported here. Although the photochemistry of HABI produces triphenylimidazolyl radicals (TPIRs) during the process of VP‐3DP, the orthogonality of the photochemistry of HABI and photopolymerization enables the introduction of reversible cross‐links derived from HABIs in the resulting 3D‐printed objects. While photostimulation cleaves a covalent bond between two imidazoles in HABI to generate TPIRs only near the surface of the 3D‐printed objects, HIFU triggers cleavage in the interior of materials. In addition, HIFU travels beyond an obstacle to induce a response of HABI‐embedded cross‐linked polymers, which cannot be attainable with photostimulation. The present system would be beneficial for tuning the physical properties and recycling of various polymeric materials, but it will also open the door for pinpoint modification, healing, and reshaping of materials when coupled to various dynamic covalent materials.