Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, Tokyo, 113-8656, Japan.
Yokohama Technical Center, AGC Inc., 1-1 Suehiro-cho, Tsurumi-ku, Yokohama, 230-0045, Japan.
Macromol Rapid Commun. 2022 May;43(9):e2200038. doi: 10.1002/marc.202200038. Epub 2022 Mar 20.
The synthesis of a CF -rich perfluoropolyether (PFPE) is achieved via the fluoride-catalyzed reaction of hexafluoropropylene oxide (HFPO) with (trifluoromethyl)trimethylsilane (TMSCF , so-called Ruppert-Prakash reagent). Nucleophilic addition of a CF anion to HFPO affords an acyl fluoride via the ring-opening of HFPO, followed by fluoride elimination. Further addition of CF 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 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 ) suggests a water- and oil-repellency of this CF -rich PFPE that is higher than that of polytetrafluoroethylene (PTFE; 18.5 mN m ).
一种富 CF 的全氟聚醚(PFPE)通过六氟丙烯氧化物(HFPO)与(三氟甲基)三甲基硅烷(TMSCF,所谓的 Ruppert-Prakash 试剂)在氟化物催化下反应合成。CF 阴离子对 HFPO 的亲核加成通过 HFPO 的开环生成酰氟,然后消除氟化物。酰氟进一步与 CF 阴离子加成得到叔全氟烷氧基,它攻击 HFPO 以重新生成酰氟。通过取代聚合重复该序列得到一种新的 PFPE 作为固体,其结构通过 19 F NMR 光谱、GC-MS 和 MALDI-TOF MS 分析得到确认。热和 X 射线衍射分析显示出结晶性质。据我们所知,这是第一个结晶 PFPE 的例子。基于接触角测量,这种富 CF 的固体 PFPE(13.4 mN m)的临界表面张力表明其疏水性和疏油性高于聚四氟乙烯(PTFE;18.5 mN m)。