New catalytic route to polysulfates and polysulfonates

Bifluoride salts could yield tough polymers efficiently at industrial scales

Polysulfates and polysulfonates are exceptionally tough and impact resistant, making them useful engineering polymers. But they’ve rarely been used industrially ­because the chloride substitution chemistry often used to make carbon sulfate and carbon sulfonate links suffers from side reactions and is commercially impractical.

Researchers now report that bifluoride salts are efficient and cost-effective catalysts for the synthesis of these tough materials (Nat. Chem. 2017, DOI: 10.1038/nchem.2796). The new chemistry, developed by K. Barry Sharpless and Peng Wu of Scripps Research Institute California, Jiajia Dong of the Shanghai Institute of Organic Chemistry, and coworkers, could potentially be scaled up to industrial levels.

The new reaction is an extension of sulfur(VI) fluoride exchange (SuFEx), a click chemistry technique Sharpless and coworkers developed previously (Angew. Chem. Int. Ed. 2014, DOI: 10.1002/anie.201309399). The group initially used SuFEx, catalyzed by strongly basic “organosuperbases,” to combine silyl ethers with fluorosulfates or sulfonyl fluorides to form polysulfates or polysulfonates, respectively. But the catalysts were expensive or required high loadings, up to 10 mole %, and they reacted in unwanted ways with starting materials.

The team turned instead to acidic bifluoride catalysts—Q+[FHF]–, where Q+ is a wide range of organic and inorganic cations and the anion is a hydrogen trapped between two fluorines through a superstrong hydrogen bond. The new catalysts require tiny loadings—as low as 0.05 mole %—making the syntheses more commercially viable.

Read full article at: http://cen.acs.org/articles/95/i26/New-catalytic-route-polysulfates-polysulfonates.html

Related article at: Organic Chemistry Help Online