Multicentered self-immobilized ethylene polymerization catalysts based on functionalized titanium halide salicylaldiminate complexes for the synthesis of ultra-high-molecular-weight polyethylene
摘要:
Specific features of ethylene polymerization using a new group of catalytic systems based on ten methylalumoxane-activated titanium halide salicylaldiminato complexes functionalized with omega-vinylalkoxy groups and containing tert-butyl substituents in the phenoxide moiety were studied. The catalytic activity of the new group of activated complexes is strongly affected by the position of the omega-vinylalkoxy functional group and by the number and position of substituents in the phenoxide moiety. These factors determine the ratio of the homogeneous and heterogeneous steps of the polymerization as a result of the catalyst self-immobilization onto the polymer formed, and also the molecular characteristics of the polymer obtained at 20, 40, and 60 degrees C and ethylene pressure of 0.4 MPa. The possibility and conditions of preparing ultra-high-molecular-weight polyethylene with improved morphology were revealed.
Design of postmetallocene catalytic systems of arylimine type for olefi n polymerization: XV. Synthesis of (N-Aryl)salicylaldimine ligands containing a but-3-enyloxy group and their complexes with titanium(IV) dichloride
作者:I. I. Oleinik、I. V. Oleinik、S. S. Ivanchev、G. A. Tolstikov
DOI:10.1134/s1070428013080095
日期:2013.8
A series of (N-aryl)salicylaldimines was synthesized by the reaction of salicylaldehydes substituted in the positions 3 and 5 by bulky tert-butyl or α-cumyl groups with hydrochlorides of o-, m-, and p-(but-3-enyloxy) aniline in the presence of triethylamine. The obtained compounds formed by the reaction with TiCl2(OPr-i)2 complexes of titanium(IV) dichloride L2TiCl2.