Affiliation:
1. Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center Frontiers Science Center for Materiobiology and Dynamic Chemistry Institute of Fine Chemicals School of Chemistry and Molecular Engineering East China University of Science and Technology Meilong Road 130 Shanghai 200237 P. R. China
2. Jiangsu Province Hi‐Tech Key Laboratory for Biomedical Research School of Chemistry and Chemical Engineering Southeast University Nanjing 211189 P. R. China
Abstract
AbstractSupramolecular organic framework (SOF) has recently garnered significant research interest in the field of luminescent materials. However, SOF with room‐temperature phosphorescence emission in solution is very rare due to the quenching of dissolved oxygen and free molecular motions, which would lead to nonradiative deactivation of triplet exciton in liquid state. In this work, a 3D cationic phosphorescent SOF is synthesized through host‐guest interaction between CB[8] and a tetrahedral monomer TBBP, which can rapidly adsorb anionic guests in solution. When anionic dyes are introduced, triplet to singlet Förster resonance energy transfer (TS‐FRET) in solution can be achieved, and delayed fluorescence with large Stokes shift can be realized. Additionally, when anionic drugs are introduced, the phosphorescence of TBBP‐CB[8] can be quenched due to charge transfer, enabling the detection of drugs through phosphorescence signals. Taking advantage of the fast adsorption property of 3D SOF, an INHIBIT logic gate with three inputs and two outputs is constructed. These findings provide a novel method to prepare phosphorescent functional materials and a new pathway to construct TS‐FRET system in solution.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
Cited by
6 articles.
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