Thermal-Robust Phenoxyimine Titanium Catalysts Bearing Bulky Sidearms for High Temperature Ethylene Homo-/Co- Polymerizations

Author:

Wang Xin12,Ma Lishuang3ORCID,Wang Xiaohua12,Zhao Wenpeng12ORCID,Liu Heng12ORCID,Zhang Xuequan12,Wang Feng12

Affiliation:

1. Shandong Provincial College Laboratory of Rubber Material and Engineering, Qingdao University of Science & Technology, Qingdao 266042, China

2. Key Laboratory of Rubber-Plastics, Ministry of Education, School of Polymer Science and Engineering, Qingdao University of Science & Technology, Qingdao 266042, China

3. College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266580, China

Abstract

A family of titanium complexes (Ti1–Ti7) with the general formula LTiCl3, supported by tridentate phenoxyimine [O−NO] ligands (L1–L7) bearing bulky sidearms, were synthesized by treating the corresponding ligands with stoichiometric amount of TiCl4. All the ligands and complexes were well characterized by 1H and 13C NMR spectroscopies, in which ortho- methoxyl groups on N-aryl moieties shifted to downfield, corroborating the successful coordination reaction. Structural optimization by DFT calculations revealed that one of the phenyl groups on dibenzhydryl moiety could form π-π stacking interaction with the salicylaldimine plane, because of which the obtained titanium complexes revealed good thermal stabilities for high-temperature polymerization of ethylene. The thermal robustness of the complexes was closely related to the strength of π-π stacking interactions, which were mainly influenced by the substituents on the dibenzhydryl moieties; Ti1, Ti4 and Ti5 emerged as the three best-performing complexes at 110 °C. With the aid of such π-π stacking interactions, the complexes were also found to be active at >150 °C, although decreased activities were witnessed. Besides homopolymerizations, complexes Ti1–Ti7 were also found to be active for the high-temperature copolymerization of ethylene and 1-octene, but with medium incorporation percentage, demonstrating their medium copolymerization capabilities.

Funder

National Natural Science Foundation of China

Taishan Scholars Program

Publisher

MDPI AG

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