荧光
金属有机骨架
体外
化学
氰化物
纳米技术
材料科学
无机化学
有机化学
光学
物理
吸附
生物化学
作者
Jialuo Li,Shuai Yuan,Jun‐Sheng Qin,Jiandong Pang,Peng Zhang,Yingmu Zhang,Yanyan Huang,Hannah F. Drake,Wenshe Ray Liu,Hong‐Cai Zhou
标识
DOI:10.1002/anie.202000702
摘要
Abstract The controlled synthesis of multicomponent metal–organic frameworks (MOFs) allows for the precise placement of multiple cooperative functional groups within a framework, leading to emergent synergistic effects. Herein, we demonstrate that turn‐on fluorescence sensors can be assembled by combining a fluorophore and a recognition moiety within a complex cavity of a multicomponent MOF. An anthracene‐based fluorescent linker and a hemicyanine‐containing CN − ‐responsive linker were sequentially installed into the lattice of PCN‐700. The selective binding of CN − to hemicyanine inhibited the energy transfer between the two moieties, resulting in a fluorescence turn‐on effect. Taking advantage of the high tunability of the MOF platform, the ratio between anthracene and the hemicyanine moiety could be fine‐tuned in order to maximize the sensitivity of the overall framework. The optimized MOF‐sensor had a CN − ‐detection limit of 0.05 μ m , which is much lower than traditional CN − fluorescent sensors (about 0.2 μ m ).
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