Alkylphenyl-Substituted Bis(salicylaldiminato) Titanium Catalysts in Ethene Polymerization

2007 ◽  
Vol 26 (15) ◽  
pp. 3690-3698 ◽  
Author(s):  
Antti Pärssinen ◽  
Tommi Luhtanen ◽  
Martti Klinga ◽  
Tapani Pakkanen ◽  
Markku Leskelä ◽  
...  
ACS Catalysis ◽  
2021 ◽  
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Author(s):  
Manfred Manßen ◽  
Danfeng Deng ◽  
Cameron H. M. Zheng ◽  
Rebecca C. DiPucchio ◽  
Dafa Chen ◽  
...  

2003 ◽  
Vol 89 (7) ◽  
pp. 1800-1807 ◽  
Author(s):  
Aihua He ◽  
Baochen Huang ◽  
Shuke Jiao ◽  
Youliang Hu
Keyword(s):  

2006 ◽  
Vol 25 (2) ◽  
pp. 463-471 ◽  
Author(s):  
Kirill V. Axenov ◽  
Ilkka Kilpeläinen ◽  
Martti Klinga ◽  
Markku Leskelä ◽  
Timo Repo

2005 ◽  
Vol 11 (14) ◽  
pp. 4078-4088 ◽  
Author(s):  
Xisheng Wang ◽  
Xingwang Wang ◽  
Hongchao Guo ◽  
Zheng Wang ◽  
Kuiling Ding
Keyword(s):  

2010 ◽  
Vol 75 (1) ◽  
pp. 105-119 ◽  
Author(s):  
Vojtech Varga ◽  
Jiří Pinkas ◽  
Róbert Gyepes ◽  
Petr Štěpnička ◽  
Michal Horáček ◽  
...  

Protocols for obtaining defined zirconocene complexes with polyhedral oligomeric silsesquioxanes with mono-, di-, and trisilanol functionality (SIPOSS, DIPOSS, and TRIPOSS) were established. The TRIPOSS silanolates binding one zirconocene and one chlorozirconocene moiety, [{(c-C5H9)7Si7O9O3}Zr2Cl(η5-C5H4R)4] (1, R = Bu; 2, R = H), were obtained by reacting the silanol with the respective zirconocene dichloride and triethylamine in CH2Cl2 in a 1.0:3.0:3.0 molar ratio, an excess of the zirconocene dichloride being required to suppress intramolecular dehydration of TRIPOSS. The related SIPOSS complex, [{(c-C5H9)7Si8O12O}2Zr(η5-C5H4Bu)2] (3), was prepared similarly at the stoichiometric ratio of [ZrCl2(η5-C5H4Bu)2]/ SIPOSS/NEt3 equal to 1.0:2.0:2.0. When employed in the 1.0:1.0:1.0 ratio, the same reagents afforded only the impure complex [{(c-C5H9)7Si8O12O}ZrCl(η5-C5H4Bu)2] (4), contaminated with 3 and unreacted [ZrCl2(η5-C5H4Bu)2]. Finally, the zirconocene complexes with SIPOSS and DIPOSS moiety, [{(c-C5H9)7Si8O12O}2Zr(η5-C5H5)2] (5) and [(c-C5H9)7Si7O9(OSiMe3)O2}- Zr(η5-C5H5)2] (6), respectively, were obtained by reacting [ZrMe2(η5-C5H5)2] with stoichiometric amounts of the appropriate silanols. All complexes were characterized by 1H, 13C, 29Si NMR and IR spectra, and by elemental analysis from XPS spectra. Preliminary ethene polymerization experiments showed that compounds 5 or 6 when combined with an excess of methylaluminoxane were nearly as active as [ZrCl2(η5-C5H5)2] whereas compound 2 was by about one order of magnitude less active.


1996 ◽  
Vol 100 (26) ◽  
pp. 11062-11066 ◽  
Author(s):  
V. J. Ruddick ◽  
P. W. Dyer ◽  
G. Bell ◽  
V. C. Gibson ◽  
J. P. S. Badyal

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