Ligand-Directed Regioselectivity in Amine–Imine Nickel-Catalyzed 1‑Hexene Polymerization

• Published in: ACS catalysis 2015-01, Vol.5 (1), p.122-128
• Main Authors: Hu, Haibin, Gao, Haiyang, Chen, Darui, Li, Guiliang, Tan, Yingxin, Liang, Guodong, Zhu, Fangming, Wu, Qing
• Format: Article
• Language: English
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/cs501081a

1-Hexene polymerizations were carried out with amine–imine nickel complexes [(ArNC­(R1)–(R2R3)­CNHAr)­NiBr2, 1a, R1 = R2 = R3 = Me, Ar = 2,6-(iPr)2C6H3; 1b, R1 = R2 = R3 = Me, Ar = 2,6-(Me)2C6H3; 2a, R1 = Me, R2 = R3 = H, Ar = 2,6-(iPr)2C6H3; 3a, R1 = Me, R2 = tBu, R3 = H, Ar = 2,6-(iPr)2C6H3] in the presence of MMAO or Et2AlCl. The ligand-directed regioselectivity involving insertion fashion and chain walking in amine–imine nickel-catalyzed 1-hexene polymerization is clearly observed. Catalyst 1a with two methyl substituents on the bridging carbon can polymerize 1-hexene to afford semicrystalline “polyethylene” with long methylene sequence (−(CH2) n –, n = 40–74) via a combination of 90% selectivity of 2,1-insertion fashion and precise chain walking, whereas catalyst 3a with a tert-butyl on the bridging carbon can polymerize 1-hexene in 80% selectivity of 1,2-insertion to produce amorphous polyolefin with predominant methyl branches through 2,6-enchainment.