荧光
材料科学
共价键
硼
共价有机骨架
分子
聚集诱导发射
路易斯酸
多孔性
纳米技术
吡啶
猝灭(荧光)
光化学
有机化学
催化作用
化学
复合材料
物理
量子力学
作者
Yuqing Sun,Bo Zhang,Caili Zhang,Huiming Lu,Yuan Yang,Bingyang Han,Fenghao Dong,Jiawei Lv,Shengjun Zhang,Zhao Li,Ziqiang Lei,Hengchang Ma
标识
DOI:10.1021/acsami.2c20580
摘要
Highly fluorescent covalent organic frameworks (COFs) are rarely obtained because of the π-π stacked layers with aggregation-caused quenching behavior. Unarguably, highly fluorescent COFs with tunable emission colors are even more rarely achieved. Herein, a general strategy to modify the classical COF material (named COF-1) by different fluorescent molecules via N → B interaction was developed. In this method, the boron-containing COF-1 acted as a porous and crystalline matrix as well as a reaction partner of Lewis acid; after interacting with fluorescent molecules with the anchoring group of pyridine (Lewis base), COF-1 takes a gorgeous transfiguration from a non-emissive powder into a highly fluorescent COF material with tunable emission colors. This disclosed method endowed the typical COFs with new emissive life and is speculated with the general research concept for all boron-containing COFs. Benefiting from the prominent fluorescent emission in the aggregation state, sensitive probes toward amines are achieved.
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