Single-Site β-Diiminate Zinc Catalysts for the Ring-Opening Polymerization of β-Butyrolactone and β-Valerolactone to Poly(3-hydroxyalkanoates)

Polymerization of â-butyrolactone (BBL) and â-valerolactone (BVL) using the zinc alkoxide initiator (BDI-1)ZnOiPr [(BDI-1) ) 2-((2,6-diisopropylphenyl)amido)-4-((2,6-diisopropylphenyl)imino)-2-pentene] proceeds very rapidly under mild conditions to produce poly(3-hydroxybutyrate) (PHB) and poly(3hydroxyvalerate) (PHV), respectively. For the monomer-to-initiator ratio 200:1, PHB number-average molecular weights (Mn) are proportional to conversion throughout the reaction and polydispersity indices (PDIs) are narrow, consistent with a living polymerization. Higher monomer-to-initiator ratios can be used to achieve high molecular weight PHB (Mn > 100 000). End-group analysis verifies that the polymerization of BBL follows a coordination-insertion mechanism, where complexes of the form (BDI-1)ZnOCH(Me)CH2CO2R are the active species. Variable temperature NMR experiments show that (BDI-1)ZnOiPr is monomeric in benzene-d6 solution. In contrast, (BDI-2)ZnOiPr [(BDI-2) ) 2-((2,6-diethylphenyl)amido)-4-((2,6-diethylphenyl)imino)-2-pentene] is a poor initiator at room temperature because it prefers to form a bis-μisopropoxide dimer in solution. According to kinetic studies, propagation by (BDI-1)ZnOiPr is first order in both monomer as well as (BDI-1)ZnOiPr concentration. These results lead us to propose a monometallic active species. Several results suggest that elimination side reactions are slowly catalyzed by zinc alkoxides, leading to degradation of the polymer.