4.7 Article

Air- and water-stable Lewis acids: synthesis and reactivity of P-trifluoromethyl electrophilic phosphonium cations

Journal

CHEMICAL COMMUNICATIONS
Volume 54, Issue 6, Pages 662-665

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cc09128a

Keywords

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Funding

  1. Royal Society of Chemistry
  2. University of Manchester
  3. NSERC of Canada
  4. Canada Research Chair
  5. EPSRC [EP/K03099X/1, EP/M023346/1]
  6. Engineering and Physical Sciences Research Council [EP/M023346/1, EP/K03099X/1, 1537618] Funding Source: researchfish

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A new class of electrophilic phosphonium cations (EPCs) containing a -CF3 group attached to the phosphorus(V) center is readily accessible in high yields, via a scalable process. These species are stable to air, water, alcohol and strong Bronsted acid, even at raised temperatures. Thus, P-CF3 EPCs are more robust than previously reported EPCs containing P-X moieties (X = F, Cl, OR), and despite their reduced Lewis acidity they function as Lewis acid catalysts without requiring anhydrous reaction conditions.

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