化学
光动力疗法
多元统计
共价键
药物输送
偶氮苯
组合化学
催化作用
过氧化氢
共价有机骨架
金属有机骨架
钯
光化学
纳米技术
吸收(声学)
辐照
卟啉
合理设计
活性氧
定义明确
烷基
分子工程
作者
Andrés Rodríguez‐Camargo,Erdost Yıldız,Diego Juela,Felix Richard Fischer,Daniel Gräf,Bibhuti Bhusan Rath,Christian Ochsenfeld,Matthias Bauer,Metin Sitti,Liang Yao,Bettina V. Lotsch
摘要
Covalent organic frameworks (COFs) have been emerging as versatile reticular materials due to their tunable structures and functionalities, enabled by precise molecular engineering at the atomic level. While the integration of multiple components into COFs has substantially expanded their structural complexity, the strategic engineering of diverse functionalities within a single framework via the random distribution of linkers with varying lengths remains largely unexplored. Here, we report a series of highly crystalline mixed-length multivariate COFs synthesized using azobenzene and bipyridine as linkers, where tuning the ratio of linkers and incorporating palladium effectively modulates the balance between near-infrared (NIR) light absorption and catalytic sites for NIR-generation of hydrogen peroxide (H2O2). Capitalizing on the deep tissue penetration of NIR light and the generated H2O2 as reactive oxygen species, as a proof of concept, the optimal mixed-length multivariate COF reduces breast cancer cell viability by almost 90% after 1 h of irradiation in a combined in vitro photodynamic therapy and drug delivery.
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