Tetradentate schiff base ligand/MCln initiating systems for the controlled cationic polymerization of isobutyl vinyl ether: Effects of the ligand framework

Abstract

ABSTRACTWe investigated the cationic polymerization of vinyl ethers using metal complex catalysts with salen and salphen ligands. Metal complexes were generated in situ from the reaction of a ligand and a metal chloride. The choice of a ligand and a central metal was crucial for tuning the catalyst function such as catalytic activity and controllability of the polymerization. Among metal chlorides employed, ZrCl4 was the most efficient for controlled polymerization. Cationic polymerization of isobutyl vinyl ether (IBVE) proceeded using the salen and salphen‐type ligand/ZrCl4 initiating systems, yielding polymers with predetermined molecular weights and narrow molecular weight distributions. Importantly, the structural effects of the complex catalysts were responsible for the polymerization behavior. For example, the polymerization using the salen‐type ligand/ZrCl4 system was much slower than that using the salphen‐type ligand/ZrCl4 system. In addition, the polymerization of IBVE using the salen‐type ligand/FeCl3 system proceeded in a controlled manner, which was in contrast to uncontrolled polymerization using the salphen‐type ligand/FeCl3 system. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 989–996