荧光
共价键
荧光团
离子键合
材料科学
猝灭(荧光)
生命科学中的荧光
离子液体
质子
剥脱关节
离子
光化学
纳米技术
化学
有机化学
石墨烯
物理
催化作用
量子力学
作者
Harpreet Singh,Manisha Devi,Nityasagar Jena,Mohamed Musthafa Iqbal,Yogendra Nailwal,Abir De Sarkar,Santanu Kumar Pal
标识
DOI:10.1021/acsami.9b20743
摘要
The exfoliation of covalent organic frameworks into covalent organic nanosheets (CONs) not only helps to reduce fluorescence turn-off phenomena but also provides well-exposed active sites for fast response and recovery for various applications. The present work is an example of rational designing of a structure constructed by condensing triaminoguanidinium chloride (TGCl), an intrinsic ionic linker, with a fluorophore, 2, 5-dimethoxyterephthalaldehyde (DA), to produce highly fluorescent self-exfoliable ionic CONs (DATGCl-iCONs). These fluorescent iCONs are able to sense fluoride ions selectively down to the ppb level via the fluorescence turn-off mechanism. A closer look at the quenching mechanism via NMR, zeta potential measurement, lifetime measurement, and density functional theory calculations reveals unique proton-triggered fluorescence switching behavior of newly synthesized DATGCl-iCONs.
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