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  • Title: Group 3 metal complexes supported by tridentate pyridine- and thiophene-linked bis(naphtholate) ligands: synthesis, structure, and use in stereoselective ring-opening polymerization of racemic lactide and beta-butyrolactone.
    Author: Grunova E, Kirillov E, Roisnel T, Carpentier JF.
    Journal: Dalton Trans; 2010 Aug 07; 39(29):6739-52. PubMed ID: 20631952.
    Abstract:
    Scandium, yttrium and lanthanum amido complexes supported by tridentate bis(ortho-silyl-substituted naphtholate)-donor ligands ({ONO(SiPh3)}(2-) and {ONO(SitBuMe2)}(2-), donor = 2,6-pyridine; {OSO(SiPh3)}(2-), donor = 2,5-thiophene) have been prepared in high yields (72-96%) by reaction of the corresponding pro-ligand {OZO(SiR3)}H(2) and Ln[N(SiHMe(2))(2)](3)(THF)(n) precursor. The solid-state structures of {ONO(SiPh3)}La[N(SiHMe(2))(2)](THF) (3), {ONO(SitBuMe2)}Ln[N(SiHMe(2))(2)](THF) (Ln = Sc, 4; Y, 5) and {OSO(SiPh3)}Ln[N(SiHMe(2))(2)](THF) (Ln = Sc, 7; La, 9) have been determined by single-crystal X-ray diffraction studies. In all five complexes, the naphtholate rings twist in the same direction from the plane of the pyridine or thiophene linker, to give rise to C(s)-symmetric (non crystallographic) structures. Compounds are 1-9 single-site initiators for the ring-opening polymerization (ROP) of racemic lactide (rac-LA) at 20 degrees C, affording poly(lactides)s (PLAs) with relatively narrow polydispersities and molecular weights in good agreement with calculated values. When carried out in THF, the polymerizations afforded heterotactic-enriched PLAs (P(r) up to 0.93), while atactic polymers are formed in toluene. Compounds 1-3 and 7-9, having o-SiPh(3) substituents on the naphtholate rings, are also active for the ROP of racemic beta-butyrolactone at 20-50 degrees C, to form syndiotactic-enriched poly(3-hydroxybutyrate)s (PHBs) (P(r) up to 0.87) when using toluene as the solvent, whereas atactic polymers were obtained in THF. The nature of the metal center (Sc, Y, La), the central linker in the ligand framework (pyridine, thiophene), and the ortho-silyl substituent (SiPh(3), SiMe(2)tBu) significantly affect the degree of stereocontrol in those polymerizations.
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