Synthesis of Crystalline CF 3 -Rich Perfluoropolyethers from Hexafluoropropylene Oxide and (Trifluoromethyl)Trimethylsilane.
Minoru KoyamaMidori AkiyamaKimiaki KashiwagiKyoko NozakiTakashi OkazoePublished in: Macromolecular rapid communications (2022)
The synthesis of a CF 3 -rich perfluoropolyether (PFPE) is achieved via the fluoride-catalyzed reaction of hexafluoropropylene oxide (HFPO) with (trifluoromethyl)trimethylsilane (TMSCF 3 , so-called Ruppert-Prakash reagent). Nucleophilic addition of a CF 3 anion to HFPO affords an acyl fluoride via the ring-opening of HFPO, followed by fluoride elimination. Further addition of CF 3 anions to the acyl fluoride gives tertiary perfluoroalkoxide, which attacks HFPO to regenerate an acyl fluoride. Repetition of the sequence via substitution-polymerization affords a new PFPE as a solid, whose structure was confirmed using 19 F NMR spectroscopy, GC-MS, and MALDI-TOF MS analysis. Thermal and X-ray diffraction analyses revealed a crystalline character. To the best of our knowledge, this is the first example of crystalline PFPE. Based on contact-angle measurements, the critical surface tension of this solid PFPE (13.4 mN m -1 ) suggests a water- and oil-repellency of this CF 3 -rich PFPE that is higher than that of polytetrafluoroethylene (PTFE; 18.5 mN m -1 ).