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Synthesis of Ladder-Type 9,9'-Bifluorenylidene-Based Conjugated Oligomers via a Pd-Catalyzed Tandem Suzuki Coupling/Heck Cyclization Approach.

Xiaoyan ZhuFeng LiuXinwu BaYonggang Wu
Published in: Organic letters (2022)
For new ladder-type oligomers and polymers with versatile and robust synthetic strategies, in this study, four fully conjugated ladder-type overcrowded 9,9'-bifluorenylidene-based compounds and oligomers ( BFY1 , BFY2 , BFY3 , and BFY4 ) were synthesized via a Pd-catalyzed tandem Suzuki coupling/Heck cyclization reaction. By monomer screening and route optimization, the target products were obtained in high yields and characterized by 1 H and 13 C NMR spectroscopy and high resolution mass spectroscopy.
Keyphrases
  • high resolution
  • room temperature
  • photodynamic therapy
  • mass spectrometry
  • single molecule
  • ionic liquid
  • electron transfer
  • visible light
  • transition metal