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Core–Shell Structured Cyclodextrin Metal–Organic Frameworks with Hierarchical Dye Encapsulation for Tunable Light Emission
Existing core–shell structured metal–organic frameworks (MOFs) are typically constructed by epitaxial growth with metal or/and organic ligands (the two basic components for MOFs) changing from core to shell, whereas in this contribution, we propose a new concept for constructing core–shell structure...
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Published in: | Chemistry of materials 2019-02, Vol.31 (4), p.1289-1295 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Existing core–shell structured metal–organic frameworks (MOFs) are typically constructed by epitaxial growth with metal or/and organic ligands (the two basic components for MOFs) changing from core to shell, whereas in this contribution, we propose a new concept for constructing core–shell structured MOF featuring hierarchic encapsulation of various guest molecules into the framework. The cyclodextrin metal–organic frameworks (CD-MOFs) were chosen as the host to encapsulate organic dyes for light-emitting applications, and the cavity structure of γ-cyclodextrin and cage structure of MOF exhibited remarkable synergistic effects on fluorescence enhancement. Furthermore, core–shell structured CD-MOFs with hierarchical encapsulation of different dyes were developed to realize polychromatic light emitting via spectrum superposition. On the basis of this new method, we further fabricated a white-light emitting core–shell crystal, CD-MOF⊃7-HCm@FL@RhB (shell@core). With three sequentially formed and adjustable layers of different dyes, the core–shell crystal emitted bright white light with a CIE coordinate of (0.35, 0.32). Our approach provides a new method for the rational design of multicolor emission crystals. Meanwhile, our findings may stimulate future investigations on multifunctional host–guest systems in crystalline state. |
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ISSN: | 0897-4756 1520-5002 |
DOI: | 10.1021/acs.chemmater.8b04126 |