Cyclic Carbonate Formation from Epoxides and CO2 Catalyzed by Sustainable Alkali Halide-Glycol Complexes: A DFT Study to Elucidate Reaction Mechanism and Catalytic Activity
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We provide a comprehensive DFT investigation of the mechanistic details of CO2 fixation into styrene oxide to form styrene carbonate, catalyzed by potassium iodide-tetraethylene glycol complex. A detailed view on the intermediate steps of the overall reaction clarifies the role of hydroxyl substances as co-catalysts for the alkali halide-catalyzed cycloaddition. The increase of iodide nucleophilicity in presence of tetraethylene glycol is examined and rationalized by NBO and Hirshfeld charge analysis, and bond distances. We explore how different alkali metal salts and glycols affect the catalytic performance. Our results provide important hints on the synthesis of cyclic carbonates from CO2 and epoxides promoted by alkali halides and glycol complexes, allowing the development of more efficient catalysts.
KeywordsDENSITY-FUNCTIONAL THERMOCHEMISTRY, ORGANIC CARBONATES, IONIC LIQUIDS, INTERMOLECULAR INTERACTIONS, PROPYLENE-OXIDE, DIOXIDE, CYCLOADDITION, FIXATION, POLY(OXYETHYLENE), TRANSFORMATION
Document typePeer reviewed
Document versionFinal PDF
SourceACS OMEGA. 2020, vol. 5, issue 29, p. 18064-18072.