共价有机骨架
紧身衣
共价键
介孔材料
堆积
光化学
光敏剂
化学
吸附
亚甲蓝
材料科学
双酚A
光催化
化学工程
荧光
有机化学
催化作用
环氧树脂
工程类
物理
量子力学
作者
Roberto Sánchez‐Naya,Florian Beuerle
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-01-09
卷期号:64 (13): e202423676-e202423676
被引量:30
标识
DOI:10.1002/anie.202423676
摘要
Abstract The direct incorporation of borondipyrromethene (BODIPY) subunits into the structural backbone of covalent organic frameworks (COFs) gives facile access to porous photosensitizers but is still a challenging task. Here, we introduce β ‐ketoenamine‐linked BDP‐TFP‐COF , which crystallizes in AA‐stacking mode with hcb topology. A comprehensive characterization reveals high crystallinity and enhanced stability in a variety of solvents, excellent mesoporosity (SA BET =1042 m 2 g −1 ), broad light absorption in the visible region, and red emission upon the exfoliation of few‐layer COF nanosheets. The versatility of multifunctional BODIPY‐COFs is highlighted in various applications. Pollutants Bisphenol A (BPA, q max =426 mg g −1 ) and Methylene Blue (MB, q max =96 mg g −1 ) have been efficiently removed from H 2 O. Fluorescence quenching or enhancement of exfoliated BDP‐TFP‐COF nanosheets have been utilized for dual‐mode sensing of MB or NEt 3 , respectively. Ultimately, the photosensitizing effect of the BODIPY units is retained in the COF. Thus, BPD‐TFP‐COF was established as a metal‐free triplet photosensitizer, which efficiently oxidized a mustard gas simulant under visible light irradiation.
科研通智能强力驱动
Strongly Powered by AbleSci AI