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Highly Tunable MOF Luminophores Featuring Anthracene Directed Assembly and Fluorescence Regulation.

Xiao-Yi LiuQiu-Ying LinHan FangXing-Wang LiShu-Ming ZhangMei-Hui YuZe Chang
Published in: Inorganic chemistry (2023)
Metal-organic frameworks (MOFs) have been recognized as a potential platform for the development of tunable luminophores owing to their highly modulable structures and components. Herein, two MOF luminophores based on Cd(II) ions, 1,3,5-tri(4-pyridinyl)benzene (TPB), and 1,4-dicarboxybenzene (H 2 BDC) were constructed. The directed assembly of the metal ions and organic linkers results in [Cd 2 (BDC) 2 (TPB)(H 2 O)]· x (solvent) ( MOF-1 ) featuring TPB-based blue fluorescence centered at 425 nm. By introducing anthracene as the structure directing agent (SDA) for assembly regulation, [Cd 2 (BDC)(TPB) 2 (NO 3 ) 2 ]· x (solvent) ( MOF-2 ) was obtained, which reveals anthracene feeding-dependent high tunable emission in the 517-650 nm range. Detailed components, photophysical properties, and structural characteristics investigations of MOF-2 indicate the TPB and NO 3 - interactions as the origin of its redshifted emission compared with that of MOF-1 . Furthermore, the fluorescence of MOF-2 was found to be regulatable by the anthracene feeding based on the SDA-determined crystallinity of the crystalline sample. All these results provided a unique example of the structural and fluorescence regulation of MOF luminophores.
Keyphrases
  • metal organic framework
  • energy transfer
  • single molecule
  • high resolution
  • room temperature
  • risk assessment
  • mass spectrometry
  • light emitting