Journal
ORGANOMETALLICS
Volume 37, Issue 9, Pages 1400-1409Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.8b00081
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Funding
- NSF [1554963]
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1554963] Funding Source: National Science Foundation
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An attractive method for valorization of glycerol is the catalytic transformation to lactic acid. By overcoming the solubility challenge associated with known homogeneous catalysts for this reaction, we show that thermally robust Ir(I), Ir(III), and Ru(II)N-heterocyclic carbene (NHC) complexes with sulfonate-functionalized wingtips are highly prolific for this process, requiring no cosolvents other than aqueous base. The activity of the catalysts is compared under both conventional heating and microwave conditions. The most active catalyst reaches a TOF of 45 592 h(-1)(microwave) and 3477 h(-1)(conventional) with 1 equiv of KOH, and proceeds at a constant rate for at least 8 h. Although higher activity is observed with KOH, the catalysts are also highly active with the weaker base, K2CO3(13 000 h(-1)and concurrent formation of formate). The protocol can be modified to achieve quantitative conversion of glycerol in only 3 h. The high activity of these catalysts compared to nonsulfonated analogs is attributed to the stabilization the lactate product in aqueous media. The most active catalyst retains equal activity for crude glycerol. A mechanism is proposed for the most active catalyst precursor involving O-H oxidative addition of glycerol.
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