- Facilely synthesized benzotriazole phenolate zirconium complexes as versatile catalysts for copolymerization of carbon dioxide with cyclohexene oxide and lactide polymerization.
Facilely synthesized benzotriazole phenolate zirconium complexes as versatile catalysts for copolymerization of carbon dioxide with cyclohexene oxide and lactide polymerization.
A family of zirconium complexes containing bis-, tri- or tetra-BTP ligands (BTP = benzotriazole phenolate) were synthesized and structurally characterized. Treatment of Zr(O(i)Pr)4((i)PrOH) with 2.0 molar equivalents of 2-(2H-benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol ((C8)BTP-H) or 2-(2H-benzotriazol-2-yl)-4,6-di-tert-butylphenol ((t-Bu)BTP-H) afforded zirconium alkoxide ([((C8)BTP)2Zr(O(i)Pr)2] (1); [((t-Bu)BTP)2Zr(O(i)Pr)2] (2)) in good yield. Similarly, the bis-adduct Zr amide [((t-Bu)BTP)2Zr(NMe2)2] (3) resulted from amine elimination of Zr(NMe2)4 as the metal precursor and (t-Bu)BTP-H as the pro-ligand under a similar synthetic method with a metal to ligand precursor ratio of 1:2 at 0 °C. The reaction of Zr(NMe2)4 with (C8)BTP-H or (t-Bu)BTP-H (4.0 mol equiv.) gave the tetra-adduct zirconium complex ([((C8)BTP)4Zr] (4); [((t-Bu)BTP)4Zr] (5)) in ≧70% yield. Interestingly, the tri-adduct Zr amide [((t-Bu)BTP)3Zr(NMe2)] (6) could be prepared by treatment of 3 with a stoichiometric amount of (t-Bu)BTP-H. The solid-state structure of 6 reveals a monomeric Zr(IV) amide with three (t-Bu)BTP ligands and one -NMe2 group, and the bonding modes between the BTP moiety and the metal centre adopt both N,O-bidentate and O-monodentate types. Zr complexes 1 and 4 incorporating sterically less bulky (C8)BTP ligands were demonstrated to efficiently catalyse not only copolymerization of epoxide with CO2 but also lactide polymerization. The tetra-BTP Zr catalyst 4 was able to copolymerize cyclohexene oxide and CO2 in a controllable manner, generating the high-molecular-weight copolymer (Mw > 10,000 g mol(-1)) and a high degree of carbonate linkages (>90%). Single-site zirconium alkoxide 1 is the most active catalyst for living lactide polymerization in solution among these complexes, giving poly(lactide)s with the expected molecular weights and narrow molecular weight distributions (PDI ≦ 1.25). This is a successful example of utilizing versatile benzotriazole phenolate Zr(IV) catalysts for either the production of biodegradable poly(lactide) or poly(cyclohexene carbonate-co-cyclohexene oxide).