Heterogeneous Epoxide Carbonylation by Cooperative Ion-Pair Catalysis in Co(CO)

• Main Authors: Park, Hoyoung Daniel (Contributor), Dinca, Mircea (Contributor), Roman, Yuriy (Contributor)
• Other Authors: Massachusetts Institute of Technology. Department of Chemical Engineering (Contributor), Massachusetts Institute of Technology. Department of Chemistry (Contributor)
• Format: Article
• Language: English
• Published: American Chemical Society (ACS), 2018-01-23T19:54:25Z.
• Subjects: Article
• Online Access: Get fulltext

Despite the commercial desirability of epoxide carbonylation to β-lactones, the reliance of this process on homogeneous catalysts makes its industrial application challenging. Here we report the preparation and use of a Co(CO)₄ - -incorporated Cr-MIL-101 (Co(CO)₄ Cr-MIL-101, Cr-MIL-101 = Cr₃O(BDC)₃F, H₂BDC = 1,4-benzenedicarboxylic acid) heterogeneous catalyst for the ring-expansion carbonylation of epoxides, whose activity, selectivity, and substrate scope are on par with those of the reported homogeneous catalysts. We ascribe the observed performance to the unique cooperativity between the postsynthetically introduced Co(CO)₄ - and the site-isolated Lewis acidic Cr(III) centers in the metal-organic framework (MOF). The heterogeneous nature of Co(CO)₄ Cr-MIL-101 allows the first demonstration of gas-phase continuous-flow production of β-lactones from epoxides, attesting to the potential applicability of the heterogeneous epoxide carbonylation strategy.
National Science Foundation (U.S.) (Award DMR-1452612)
United States. Department of Energy. Office of Basic Energy Sciences (Award DE-SC0016214)