Immortal ring-opening polymerization of β-butyrolactone with zinc catalysts: Catalytic approach to poly(3-hydroxyalkanoate)

The zinc alkoxide complex prepared in situ from the reaction of (BDI)Zn(N(SiMe3)(2)) (BDI=2-((2,6-diisopropylphenyl)amido)-4-((2,6-diisopropylphenyl)imino)-2-pentene) with ROH (R=iPr or Bn=CH2Ph) is an efficient catalyst for both the solution and bulk ring-opening polymerization (ROP) of racemic-beta-butyrolactone (BBL). The controlled immortal ROP of BBL using the binary catalytic system (BDI)Zn(N(SiMe3)(2))/BnOH, where the alcohol acts both as co-initiator and chain transfer agent, proceeds smoothly under mild conditions (solution or bulk, 23-90 degrees C) to produce atactic poly(3-hydroxybutyrate) with moderate to high molar mass. For the first time, PHBs could be prepared from very small loadings of a metallic catalyst (100 ppm) via an immortal procedure, thereby allowing the growth of as many as 50-200 PHBs chains per metal center. Well-defined alpha-hydroxy, omega-alkoxy ester telechelic PHBs, of molar mass ranging up to (M) over barn = 42, 600 g mol(-1) were thus quantitatively obtained and fully characterized by NMR, MALDI-TOF MS and SEC analyses. (C) 2009 Elsevier Ltd. All rights reserved.