Effect of ketimide ligand for ethylene polymerization and ethylene/norbornene copolymerization catalyzed by (cyclopentadienyl)(ketimide)titanium complexes–MAO catalyst systems: Structural analysis for Cp∗TiCl2(NCPh2)

2007 ◽  
Vol 692 (21) ◽  
pp. 4675-4682 ◽  
Author(s):  
Kotohiro Nomura ◽  
Junji Yamada ◽  
Wei Wang ◽  
Jingyu Liu
2001 ◽  
Vol 30 (6) ◽  
pp. 566-567 ◽  
Author(s):  
Tomoaki Matsugi ◽  
Shigekazu Matsui ◽  
Shin-ichi Kojoh ◽  
Yukihiro Takagi ◽  
Yoshihisa Inoue ◽  
...  

2013 ◽  
Vol 135 (34) ◽  
pp. 12592-12595 ◽  
Author(s):  
Dana Shoken ◽  
Manab Sharma ◽  
Mark Botoshansky ◽  
Matthias Tamm ◽  
Moris S. Eisen

1994 ◽  
Vol 89 (1-2) ◽  
pp. 41-50 ◽  
Author(s):  
Giuseppe Conti ◽  
Guillermo Arribas ◽  
Angelina Altomare ◽  
Francesco Ciardelli

2016 ◽  
Vol 3 (1) ◽  
Author(s):  
I.E. Soshnikov ◽  
N.V. Semikolenova ◽  
A.A. Antonov ◽  
K.P. Bryliakov ◽  
V.A. Zakharov ◽  
...  

AbstractIn this work, previously undetected intermediates of several practically promising catalyst systems for ethylene polymerization and trimerization are discussed. In particular, the activation of ethylene polymerization catalysts (1) LNiCl2 (L = 2,4,6-trimethyl- (N-5,6,7-trihydroquinolin-8-ylidene)phenylamine) with AlEt2Cl and AlMe2Cl, (2) activation of bis(imino)pyridine vanadium(III) chloride L1VIIICl3 (L1 = 2,6-(ArN=CMe)2C5H3N, Ar = 2,6-iPr2C6H3; 2,6-Me2C6H3; 2,4,6-Me3C6H2; 3,5- F2C6H3) with AlMe3/[Ph3C]+[B(C6F5)]4¯ and MAO, and (3) selective ethylene trimerization catalyst (FI)TiCl3 (FI = phenoxyimine ligand with an additional aryl-OCH3 donor) with MAO have been assessed by NMR and EPR spectroscopy. The nature of ion-pair intermediates – the closest precursors of the propagating species – has been established, and the major catalyst deactivation pathways are discussed.


2012 ◽  
Vol 31 (17) ◽  
pp. 6085-6094 ◽  
Author(s):  
Shaneesh Vadake Kulangara ◽  
Amir Jabri ◽  
Yun Yang ◽  
Ilia Korobkov ◽  
Sandro Gambarotta ◽  
...  

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