Zwitterionic niobium and tantalum complexes with bidentate aminophenol scaffolds: synthesis, structural characterization and use in the ring opening polymerization of lactides†
Abstract
The stoichiometric reaction of the aminophenol ligands L1–L3 with NbCl5 or TaCl5 afforded a series of metal chloride complexes 1–6. These were characterized by 1H, 13C NMR, mass spectroscopy and elemental analysis. Complex 2 crystallized as ethoxy substituted complex 2a upon attempting crystallization from a solvent mixture of chloroform and ethanol. The molecular structure confirms the zwitterionic nature of the complex where the protonated nitrogen atom of the ligand backbone is neutralised by a negative charge on the metal center. Moderate electrostatic hydrogen bonding interactions between the NH+ donor moieties and acceptor chlorine atoms stabilise these complexes. The complexes show moderate activities towards the ring opening polymerization (ROP) of lactides (rac-LA, L-LA) with good control over the polymerization parameters. All the complexes produced heterotactic enriched poly(lactic acid) (PLA). Low molecular weight oligomers prepared and analysed by MALDI-TOF mass and 1H NMR spectroscopy revealed that the ligand initiates the ROP. The complexes were optimized at the B3LYP/LANL2DZ level and the frontier orbitals were studied in order to calculate the trend in reactivity order theoretically.
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