An operationally mild, ruthenium-based photocatalytic protocol has been developed for the conversion of gamma-mono- and gamma,gamma-disubstituted allyl carbonates in the presence of Umemoto's reagent to afford substituted six-membered cyclic carbonates. Variation and diversification of the carbonate ring substitution provides access to new monomers useful in ring-opening polymerization leading to polycarbonates with potentially tailored properties, as illustrated by comparative experiments using monomers with different pi-stacking capabilities.

Photocatalytic Synthesis of Substituted Cyclic Carbonate Monomers for Ring-Opening Polymerization

Della Monica F;
2021-01-01

Abstract

An operationally mild, ruthenium-based photocatalytic protocol has been developed for the conversion of gamma-mono- and gamma,gamma-disubstituted allyl carbonates in the presence of Umemoto's reagent to afford substituted six-membered cyclic carbonates. Variation and diversification of the carbonate ring substitution provides access to new monomers useful in ring-opening polymerization leading to polycarbonates with potentially tailored properties, as illustrated by comparative experiments using monomers with different pi-stacking capabilities.
2021
https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.202100654
Maquilon, C; Della Monica, F; Limburg, B; Kleij, Aw
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/2129322
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