Tetraphenylethylene-Decorated Metal-Organic Frameworks as Energy-Transfer Platform for the Detection of Nitro-Antibiotics and White-Light Emission.

Inorg Chem

Collaborative Innovation Center of Water Security for Water Source Region of Mid-line of South-to-North Diversion Project of Henan Province , Nanyang Normal University, Nanyang 473061 , P. R. China.

Published: October 2019

AI Article Synopsis

  • Highly porous luminescent metal-organic frameworks (MOFs) can be used as fluorescent probes for detecting nitro compounds and as containers for host-guest systems.
  • Two new 3D MOFs were created using a specific ligand (tppe), showing particularly high sensitivity and selectivity for detecting nitro-antibiotics like furazolidone (FZD).
  • The research also demonstrates that these MOFs can emit white light when sulforhodamine 101 (SR101) is encapsulated within their structure, enhancing their versatility.

Article Abstract

The highly porous luminescent metal-organic frameworks (MOFs) can act as fluorescent probes for the detection of nitro compounds and can also serve as containers and energy transfer platforms to construct the host-guest systems. Herein, two new three-dimensional MOFs with high porosity were prepared successfully by the electron-rich tetrakis(4-pyridylphenyl)ethylene (tppe) as ligands. Compound shows the high sensitivity and selectivity toward nitro-antibiotics in an aqueous media, particularly showing the best detection efficiency for furazolidone (FZD) among the reported luminescent sensors. The highly efficient fluorescence quenching toward FZD may be attributed to the electron and energy transfer. Compound has naphthalene-2,7-dicarboxylic acid (2,7-npd) and tppe as dual linkers, and the energy transfer between 2,7-npd and tppe leads to the emission band in a large scale. It is worth noting that the single-phased white-light materials can be obtained by the in situ encapsulation of different concentration of sulforhodamine 101 (SR101) into compound matrix.

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Source
http://dx.doi.org/10.1021/acs.inorgchem.9b01588DOI Listing

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