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Updated: Jul 22, 2025

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
The preparation of hexaphenylsilole-based conjugated microporous polymer for fluorescence sensing o-nitrophenol
Feng Zhu1, Kang Wang1, Tongmou Geng1
1Collaborative Innovation Center for Petrochemical New Materials, AnHui Province Key Laboratory of Optoelectronic and Magnetism Functional Materials, Anqing Normal University, Anqing 246011, PR China.
Abstract:
A first hexaphenylsilole-based conjugated microporous polymer, termed THPS, was prepared by a Friedel-Crafts arylation reaction of 1,1,2,3,4,5-hexabenylthirole with 2,4,6-trichloro-1,3,5-triazine catalyzed by anhydrous aluminium trichloride (AlCl3) in 1,2-dichloroethane. Its Brunauer-Emmett-Teller and Langmuir surface area reached up to 1579 and 2081 m2 g-1, and total pore volume and micropore pore volume were severally 0.8325 and 0.7322 cm3 g-1. THPS could fluorescence-sense o-nitrophenol with high sensitivity and selectivity. Its fluorescence quenching constant (KSV) and limits of detection (LODs) were severally 8.32 × 103 L mol-1 and 3.61 × 10-10 mol L-1. The fluorescence quenching of THPS by o-nitrophenol was originated from the combined action of both photo-induced electron transfer mechanism and resonance energy transfer mechanism.

