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

堆积 部分 共聚物 高分子化学 乙烯 催化作用 化学计量学 化学 聚合 材料科学 结晶学 有机化学 聚合物
作者
Xin Wang,Lishuang Ma,Xiaohua Wang,Wenpeng Zhao,Heng Liu,Xuequan Zhang,Feng Wang
出处
期刊:Polymers [MDPI AG]
卷期号:16 (7): 902-902
标识
DOI:10.3390/polym16070902
摘要

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.
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