When Bigger is Better: Lanthanum Complexes of Bis(phenoxy‐amidine) FAlen Ligands as Unique Catalysts for the Isoselective Ring‐Opening Polymerization of Racemic β‐Lactones

T Thanh‐Tu Bui (Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes (UMR 6226) Rennes F‐35042 France) J Jérôme Bayardon (Univ Bourgogne Europe, CNRS, ICMUB (UMR 6302) Dijon F‐21000 France) C Cédric Balan (Univ Bourgogne Europe, CNRS, ICMUB (UMR 6302) Dijon F‐21000 France) T Thierry Roisnel (Universite de Rennes) R Raluca Malacea‐Kabbara (Univ Bourgogne Europe, CNRS, ICMUB (UMR 6302) Dijon F‐21000 France) P Pierre Le Gendre (Univ Bourgogne Europe, CNRS, ICMUB (UMR 6302) Dijon F‐21000 France) E Evgueni Kirillov (Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes (UMR 6226) Rennes F‐35042 France) J Jean‐François Carpentier (Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes (UMR 6226) Rennes F‐35042 France)

Abstract

Abstract Discrete yttrium and lanthanum complexes supported by new bis(phenoxy‐amidine) ligands have been prepared in high yields. Some of these so‐called FAlen ligands, when coordinated onto the large La 3+ in contrast to the small Y 3+ , can adopt an η 3 coordination mode of both amidine moieties. These La‐FAlen complexes, either previously isolated or conveniently prepared in situ, act as highly efficient ROP catalysts of simple and functional β‐propiolactones rac ‐BL R (R = Me, CH 2 O i Pr, CH 2 OSi t BuMe 2 ) under mild conditions, returning the corresponding linear polymers PBL R with high control over the molecular weights and narrow dispersities. More uniquely, when substituents with appropriate bulkiness are installed on the phenoxy and amidine moieties, the polymers all feature high isotacticity ( P m up to 0.93). High activity and isoselectivity are maintained, no matter the nature and polarity of the solvent used.

Article Details

Volume / Issue Vol. 64, Issue 36
Published September 01, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

T

Thanh‐Tu Bui

Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes (UMR 6226) Rennes F‐35042 France

J

Jérôme Bayardon

Univ Bourgogne Europe, CNRS, ICMUB (UMR 6302) Dijon F‐21000 France

C

Cédric Balan

Univ Bourgogne Europe, CNRS, ICMUB (UMR 6302) Dijon F‐21000 France

T

Thierry Roisnel

Universite de Rennes

R

Raluca Malacea‐Kabbara

Univ Bourgogne Europe, CNRS, ICMUB (UMR 6302) Dijon F‐21000 France

P

Pierre Le Gendre

Univ Bourgogne Europe, CNRS, ICMUB (UMR 6302) Dijon F‐21000 France

E

Evgueni Kirillov

Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes (UMR 6226) Rennes F‐35042 France

J

Jean‐François Carpentier

Univ Rennes, CNRS, Institut des Sciences Chimiques de Rennes (UMR 6226) Rennes F‐35042 France