Synthesis and characterization of novel chromium complexes based on β-enaminoketonato ligands and their application to ethylene polymerization

被引:5
|
作者
Liu, Jing-Yu [1 ]
Tao, Ping [1 ]
Li, Yue-Sheng [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
Ziegler-Natta polymerization; Catalysts; Polyolefin; TITANIUM COMPLEXES; ACTIVE CATALYSTS; TRIMERIZATION; OLIGOMERIZATION; BEARING; OLEFINS; COPOLYMERIZATION; NITROGEN;
D O I
10.1016/j.molcata.2014.07.006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of novel non-Cp-based chromium(III) complexes bearing tridentate beta-enaminoketonato chelating ligands of type, [(RNC)-N-2(CF3)C(H)(CRO)-O-1]CrCl2(thf) (2a: R-1 = Bu-t, R-2 = -C6H4OMe(o); 2b: R-1 = Bu-t, R-2 = -C9H6N; 2c: R-1 = Bu-t, R-2 = -C6H4SMe(o); 2d: R-1 =Ph, R-2 = -C9H6N; 2e: R-1 = Ph, R-2 = -C6H4SMe(o)) have been prepared in high yields (e.g. 63-79%) from CrCl3(thf)(3) by treating with 1.0 equiv. of the deprotonated ligands in tetrahydrofuran. These complexes were identified by IR, and mass spectra as well as elemental analysis. Structures for 2b, 2c and 2e were further confirmed by X-ray crystallography. Non-Cp-based chromium(III) complexes have six-coordinate distorted octahedral geometry, and the heteroatom in the sidearm is coordinated to chromium. When activated by modified methylaluminoxane, complexes 2b and 2c exhibited high activities towards ethylene polymerization. These results indicated that both the donor atoms in side arm and the substituents in backbone significantly affected polymerization behaviors. In order to further explore the structure-reactivity relationship of the catalysts, we synthesized some novel half-sandwich chromium(III) complexes, Cp[(RNC)-N-2(CF3)C(H)(CRO)-O-1]CrCl (3a: R-1 = Bu-t, R-2 = -C6H4OMe(o); 3c: R-1 = Bu-t, R-2 = -C6H4SMe(o); 3e: R-1 = Ph, R-2 = -C6H4SMe(o)) and investigated their potential application in ethylene polymerization under the similar conditions. Complex 3c adopts a three-legged piano stool geometry with a pseudo-octahedral coordination environment, and the heteroatom in the sidearm is not coordinated to chromium. These half-sandwich chromium complexes all displayed high activities for ethylene polymerization under the same conditions. Neither the donor atom in side arm nor the substituent in backbone significantly affected polymerization behaviors, in complete contrast to the results by non-Cp-based chromium catalysts. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:162 / 169
页数:8
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