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Imparting multi-functionality to covalent organic framework nanoparticles by the dual-ligand assistant encapsulation strategy

Liang Chen, Wenxing Wang, Jia Tian, Fanxing Bu, Tiancong Zhao, Minchao Liu, Runfeng Lin, Fan Zhang, Myongsoo Lee, Dongyuan Zhao and Xiaomin Li ()
Additional contact information
Liang Chen: Fudan University
Wenxing Wang: Fudan University
Jia Tian: University of Victoria
Fanxing Bu: Fudan University
Tiancong Zhao: Fudan University
Minchao Liu: Fudan University
Runfeng Lin: Fudan University
Fan Zhang: Fudan University
Myongsoo Lee: Fudan University
Dongyuan Zhao: Fudan University
Xiaomin Li: Fudan University

Nature Communications, 2021, vol. 12, issue 1, 1-10

Abstract: Abstract The potential applications of covalent organic frameworks (COFs) can be further developed by encapsulating functional nanoparticles within the frameworks. However, the synthesis of monodispersed core@shell structured COF nanocomposites without agglomeration remains a significant challenge. Herein, we present a versatile dual-ligand assistant strategy for interfacial growth of COFs on the functional nanoparticles with abundant physicochemical properties. Regardless of the composition, geometry or surface properties of the core, the obtained core@shell structured nanocomposites with controllable shell-thickness are very uniform without agglomeration. The derived bowl-shape, yolk@shell, core@satellites@shell nanostructures can also be fabricated delicately. As a promising type of photosensitizer for photodynamic therapy (PDT), the porphyrin-based COFs were grown onto upconversion nanoparticles (UCNPs). With the assistance of the near-infrared (NIR) to visible optical property of UCNPs core and the intrinsic porosity of COF shell, the core@shell nanocomposites can be applied as a nanoplatform for NIR-activated PDT with deep tissue penetration and chemotherapeutic drug delivery.

Date: 2021
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DOI: 10.1038/s41467-021-24838-7

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