Volume 95 Issue 26 | p. 6 | News of The Week
Issue Date: June 26, 2017 | Web Date: June 22, 2017

New catalytic route to polysulfates and polysulfonates

Bifluoride salts could yield tough polymers efficiently at industrial scales
Department: Science & Technology
Keywords: polymers, polysulfates, polysulfonates, catalysts, click chemistry, SuFEx, sulfur(VI) fluoride exchange

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.

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By changing the catalyst in a click chemistry reaction, researchers can make polysulfates (shown) and polysulfonates in a more efficient way.
Reaction scheme shows use of an acidic bifluoride catalyst to combine fluorosulfate and silyl ether starting materials into a polysulfate polymer.
 
By changing the catalyst in a click chemistry reaction, researchers can make polysulfates (shown) and polysulfonates in a more efficient way.

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.

Polymer chemist Saadyah Averick of the Allegheny Health Network Neuroscience Institute comments that the catalysts also extend the substrate scope to a wider range of monomers. This chemistry makes polysulfates and polysulfonates more readily available, so “applications of these materials can be fully explored,” he says.

Two companies are negotiating with Scripps to license the technology.

 
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