The role of neutral donor ligands in the isoselective ring-opening polymerization of -β-butyrolactone.

Isoenriched poly-3-hydroxybutyrate (P3HB) is a biodegradable material with properties similar to isotactic polypropylene, yet efficient routes to this material are lacking after 50+ years of extensive efforts in catalyst design. In this contribution, a novel lanthanum aminobisphenolate catalyst () can access isoenriched P3HB through the stereospecific ring-opening polymerization (ROP) of -β-butyrolactone (-BBL). Replacing the tethered donor group of a privileged supporting ligand with a non-coordinating benzyl substituent generates a catalyst whose reactivity and selectivity can be tuned with inexpensive achiral neutral donor ligands ( phosphine oxides, OPR). The /OPR (R = -octyl, Ph) systems display high activity and are the most isoselective homogeneous catalysts for the ROP of -BBL to date (0 °C: = 0.8, TOF ∼190 h). Combined reactivity and spectroscopic studies provide insight into the active catalyst structure and ROP mechanism. Both and a structurally related catalyst with a tethered donor group () operate under chain-end stereocontrol; however, favors formation of P3HB with opposite tacticity (syndioenriched) and its ROP activity and selectivity are totally unaffected by added neutral donor ligands. Our studies uncover new roles for neutral donor ligands in stereospecific ROP, including suppression of chain-scission events, and point to new opportunities for catalyst design.