光致聚合物
解聚
聚合
聚合物
软物质
化学
分子
磺酸
材料科学
光化学
化学工程
高分子化学
有机化学
胶体
工程类
作者
Mamata Ojha,Wai Lean Koay,Bhaskar Biswas,Xin Yi Oh,Quyen Thi Vu,Vinh X. Truong,N. D. Pradeep Singh
标识
DOI:10.1002/ange.202508730
摘要
Abstract Photoremovable protecting groups (PRPGs) enable precise spatiotemporal control over molecular release and functional activation. Recent advances have introduced wavelength‐selective systems for sequential deprotection, broadening applications in drug delivery, material synthesis, and photopolymerization. In parallel, PRPGs play a crucial role in photobase generators (PBGs) and photoacid generators (PAGs), enabling oxygen‐tolerant, spatially controlled polymerization and depolymerization through light‐induced base and acid release. Herein, we present a novel benzophenazine‐based photocleavable system capable of the sequential, wavelength‐selective release of both a base and an acid. This design integrates 1,1,3,3‐tetramethylguanidine (TMG) and p ‐toluene sulfonic acid functionalities, which are independently uncaged upon irradiation with blue (≥ 410 nm) and UV (≥ 310 nm) light, respectively. We demonstrated the versatility of this dual‐responsive system in modulating soft matter properties, including wavelength‐selective polymer crosslinking, degradation, and debonding‐on‐demand adhesives. This work establishes a new platform for advanced photochemical control over polymeric transformations, with broader implications in responsive soft matter engineering.
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