Screening of metal complex catalysts using bidentate Schiff base ligands for controlled cationic polymerization of vinyl ethers using complexation method

• Published in: Polymer chemistry Vol. 1; no. 3; pp. 429 - 4219
• Main Authors: Kigoshi, Sensho, Kanazawa, Arihiro, Kanaoka, Shokyoku, Aoshima, Sadahito
• Format: Journal Article
• Published: 30.07.2019
• ISSN: 1759-9954; 1759-9962
• DOI: 10.1039/c9py00351g

Various ligands were screened for the cationic polymerization of isobutyl vinyl ether (IBVE) via in situ complexation using ZrCl 4 as a catalyst precursor. [N,O]-Type phenoxyimine ligand frameworks were found to be more efficient for controlled polymerization compared to ligands that coordinate to the metal via two oxygen ([O,O]-type ligands) or two nitrogen ([N,N]-type ligands) atoms. In particular, the N -aryl phenoxyimine ligand with t Bu groups on the phenol moiety was effective in terms of the controllability of the polymerization, catalyst solubility, catalytic activity, and ease of derivatization. Moreover, optimization of reaction conditions led to the expansion of the applicable metal species for controlled cationic polymerization. The polymerization of IBVE using the N -phenyl phenoxyimine ligand/TiCl 4 initiating system in the absence of ethyl acetate in toluene at −78 °C produced a well-controlled polymer. In addition, the phenoxyimine/ZrCl 4 systems were effective for the controlled polymerization of various monomers including St derivatives. The easily tunable electronic properties were also useful for the controlled bulk polymerization. Appropriate ligand scaffolds in cationic polymerization were screened using various bidentate Schiff base ligand/ZrCl 4 initiating systems.