• Lanthanides;
  • Ligand design;
  • Polymerization


A series of lanthanide monoborohydrido complexes {C6H4-1,2-[NC(R)NR′]2}Ln(BH4)(L)n (Ln = Y, Nd, Sm; R = tBu, Ph; R′ = 2,6-Me2C6H3, SiMe3; L = dme = dimethoxyethane, n = 1; L = thf, n = 2), in which lanthanides are coordinated by bulky ansa-bis(amidinato) ligand systems with a conformationally rigid o-phenylene linker ({C6H4-1,2-[NC(R)NR′]2}2–), were synthesized by the salt metathesis reactions of equimolar amounts of Ln(BH4)3(thf)3 and {C6H4-1,2-[NC(R)NR′]2}X2(thf)n (X = Li, Na) in thf. X-ray diffraction studies revealed that the complexes are monomeric. Depending on the denticity of the donor ligand (L = dme or thf), the terminal borohydrido ligand coordinated to the metal ion can be located in either an equatorial (L = thf) or an apical (L = dme) position. All complexes are efficient catalysts for the ring-opening polymerization of rac-lactide, which allows to convert up to 1000 equiv. of monomer into a polymer at room temperature within 10–150 min and affords atactic polylactides with high molecular weights and moderate molecular-weight distributions (1.28–2.16). Yttrium–borohydrido complexes coordinated by the {C6H4-1,2-[NC(tBu)N(2,6-Me2C6H3)]2}2– ligand system showed enhanced catalytic activity compared to that of the analogue complexes containing the {C6H4-1,2-[NC(Ph)NSiMe3]2}2– ligand. The obtained borohydrido complexes catalyze the hydrophosphonylation of benzaldehyde at room temperature with good reaction rates.