Why Less Coordination Provides Higher Reactivity Chromium Phosphinoamidine Ethylene Trimerization Catalysts

ACS Catalysis ◽  
2020 ◽  
Vol 10 (17) ◽  
pp. 9674-9683
Author(s):  
Doo-Hyun Kwon ◽  
Steven M. Maley ◽  
Johnathan C. Stanley ◽  
Orson L. Sydora ◽  
Steven M. Bischof ◽  
...  
2011 ◽  
Vol 30 (19) ◽  
pp. 5297-5302 ◽  
Author(s):  
Yun Yang ◽  
Zhen Liu ◽  
Lei Zhong ◽  
Pengyuan Qiu ◽  
Qi Dong ◽  
...  

2011 ◽  
Vol 30 (15) ◽  
pp. 4159-4164 ◽  
Author(s):  
Khalid Albahily ◽  
Yacoob Shaikh ◽  
Zeeshan Ahmed ◽  
Ilia Korobkov ◽  
Sandro Gambarotta ◽  
...  

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.


2005 ◽  
Vol 24 (4) ◽  
pp. 552-556 ◽  
Author(s):  
David S. McGuinness ◽  
Peter Wasserscheid ◽  
David H. Morgan ◽  
John T. Dixon

2006 ◽  
Vol 45 (42) ◽  
pp. 7050-7053 ◽  
Author(s):  
Claire Temple ◽  
Amir Jabri ◽  
Patrick Crewdson ◽  
Sandro Gambarotta ◽  
Ilia Korobkov ◽  
...  

2014 ◽  
Vol 475 ◽  
pp. 371-378 ◽  
Author(s):  
Timur M. Zilbershtein ◽  
Vladislav A. Kardash ◽  
Vladlena V. Suvorova ◽  
Anatoly K. Golovko

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