Ring-opening polymerization (ROP) of cyclic esters/lactones by efficient catalysts is a powerful method for synthesis of biodegradable and biocompatible polyesters with well-defined structures. To develop catalytic systems that are fast, selective and controlled is a persistent effort of chemists. In this contribution, we report a binary urea/alkoxide catalytic system that could catalyze ROP of rac-LA in a fast (over 90% conversion within 1–2 min), stereoselective (Pi up to 0.93) and controlled manner, indicated by narrow MW distributions, linear relationship between the monomer conversions and Mns, end-group fidelity, and chain extension experiments. Remarkably, the catalytic system described here is simple, easily prepared, and structurally tunable and thus has versatile catalytic performances.

Chromium-based complexes are among the most important catalysts in the field of ethylene polymerization and oligomerization. Heterogeneous Cr Phillips catalysts account for more than one-third of the commercialized high density polyethylene (HDPE). In this contribution, chromium complexes, LCrCl3 (Cr1-Cr4: L = 2,6-R1-4-R2-C6H2-N[double bond, length as m-dash]CH-C6H4-2-PPh2; Cr1: R1 = H, R2 = H; Cr2: R1 = Me, R2 = H; Cr3: R1 = iPr, R2 = H; Cr4: R1 = Ph2CH, R2 = iPr), have been synthesized and characterized by elemental analysis, ESI and IR spectroscopy. The molecular structures of Cr3 and Cr4 are defined by X-ray diffraction, revealing a distorted octahedral geometry around the chromium center in both structures. In the presence of an aluminum cocatalyst, complexes Cr1-Cr4 show moderate to high activities toward ethylene polymerization. The nature of the catalysts and various reaction conditions, such as the nature and the amount of cocatalyst, reaction time and temperature, are investigated in detail. The results show that the title complexes have good thermal stability and the substituents on the ligands significantly affect the catalytic properties. Particularly, complex Cr4 can produce HDPE with a high molecular weight up to 68.3 × 104 g mol-1 due to the suppression of the chain transfer/termination by the introduction of bulky Ph2CH groups.

The aluminum complexes LAlMe2 (Al1–Al5: LH = 2,6-(R1)2-4-R2-C6H2NHCH2C6H4-2-PPh2; Al1, R1 = H, R2 = H; Al2, R1 = Me, R2 = H; Al3, R1 = i Pr, R2 = H; Al4, R1 = Ph2CH, R2 = i Pr; Al5, R1 = Cl, R2 = H) have been synthesized and characterized by elemental analysis and 1H, 13C, and 31P NMR. NMR analysis in solution reveals an interesting hemilabile coordination of the soft P donor. The molecular structures of Al2–Al4 were defined by X-ray diffraction studies, showing a distorted-tetrahedral geometry around the aluminum center in all structures. Careful comparison of these crystal structures suggested that different substituents on the ligands could lead to unignorable changed coordination environments around the Al center, thus affecting their catalytic properties. In the presence of BnOH, complexes Al1–Al5 efficiently catalyzed the ring-opening polymerization (ROP) of ε-caprolactone (ε-CL) with high conversions in a controlled manner, and high molecular weights (M n up to 118.6 kg mol–1) of polycaprolactones (PCLs) were readily prepared. Immortal polymerizations by Al4 having bulky Ph2CH groups were also studied with up to 20 equiv of alcohols and 2000 equiv of monomers, without sacrificing polymerization control.