Restoring order: YIII, EuIII, and ErIII tris(ligand) complexes of a new chiral alkoxide ligand, tBu2P(O)CH2CH(tBu)OH (HL), preferentially form as C3‐symmetric diastereomers. Thus racemic HL affords (RRR)‐ and (SSS)‐[LnL3] complexes, which are active catalysts for the stereoselective polymerization of rac‐lactide to afford highly isotactic polylactic acid.

The reaction of a chiral racemic bidentate ligand HL1 (tBu2P(O)CH2CH(tBu)OH) with mid to late trivalent lanthanide cations affords predominantly homochiral lanthanide complexes (RRR)-[Ln(L1)3] and (SSS)-[Ln(L1)3]. A series of reactions are reported that demonstrate that the syntheses are under thermodynamic control, and driven by a ligand 'self-recognition' process, in which the large asymmetric bidentate L1 ligands pack most favourably in a C3 geometry around the lanthanide cation. The synthesis of bis(L1) adducts [Ln(L1)2X] (X=N(SiMe3)2, OC6H3tBu-2,6) is also reported. Analysis of the diastereomer mixtures shows that homochiral (L1)2 complexes are favoured but to a lesser extent. The complexes Ln(L1)3 and [Ln(L1)2(OC6H3tBu-2,6)] have been studied as initiators for the polymerization of epsilon-caprolactone and its copolymer with lactide, glycolide and its copolymer with lactide, and epsilon-caprolactam.

In Ordnung gebracht: YIII‐, EuIII‐ und ErIII‐Tris(ligand)‐Komplexe des neuen chiralen Alkoxidliganden tBu2P(O)CH2CH(tBu)OH (HL) entstehen bevorzugt als C3‐symmetrische Diastereomere. Somit liefert racemisches HL (RRR)‐ und (SSS)‐[LnL3]‐Komplexe, die die stereoselektive Polymerisation von rac‐Lactid zu hoch isotaktischem Polylactid effektiv katalysieren.