Phosphinimides as a Steric Equivalent to Cyclopentadienyl: An Approach to Ethylene Polymerization Catalyst Design-Reference-Cited by-同舟云学术

Phosphinimides as a Steric Equivalent to Cyclopentadienyl: An Approach to Ethylene Polymerization Catalyst Design

Published:1999-03-01 Issue:7 Volume:18 Page:1116-1118
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Stephan Douglas W.¹,Stewart Jeffrey C.¹,Guérin Frédéric¹,Spence Rupert E. v. H.¹,Xu Wei¹,Harrison Daryll G.¹

Affiliation:

1. School of Physical Sciences, Chemistry and Biochemistry, University of Windsor, Windsor, Ontaria, Canada N9B 3P4, and NOVA Research & Technology Corporation, 2928 16 Street N.E., Calgary, Alberta, Canada T2E 7K7

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om980955e

Reference35 articles.

1. Cationic Group 4 metallocene complexes and their role in polymerisation catalysis: the chemistry of well defined Ziegler catalysts

2. Sterically Demanding Diamide Ligands: Synthesis and Structure of d0 Zirconium Alkyl Derivatives

3. Living Polymerization of α-Olefins by Chelating Diamide Complexes of Titanium

4. Neutral and Cationic Group 4 Complexes Containing Bis(borylamide) Ligands, [R2BNCH2CH2NBR2]2- (R = 2,4,6-i-Pr3C6H2, M = Zr; R = Cyclohexyl, M = Ti, Zr, Hf)

5. Novel zirconium complexes derivedfrom C2-symmetric diamide ligands; the X-ray crystal structure of [Zr(η1-CH2Ph)(η2-CH2Ph){(C6H3)2-2,2′-(NCH2C6H4Ph-4)2-6, 6′-Me2}]

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