Issue 5, 2007

Structure–reactivity relationships in SHOP-type complexes: tunable catalysts for the oligomerisation and polymerisation of ethylene

Abstract

For over 30 years complexes with the general formula [NiPh(P,O)L] (L = tertiary phosphine; P,O = chelating phosphanylenolato ligand) have been used as highly efficient oligomerisation catalysts suitable for the production of linear α-olefins. The same complexes, which are usually referred to as SHOP-type catalysts (SHOP = Shell Higher Olefin Process) can also be used as ethylene polymerisation catalysts, provided they are treated with a phosphine scavenger that selectively removes the tertiary phosphine ligand (L). This Perspective examines the impact of various parameters (influence of the substituents, backbone size, solvent, use of cocatalysts, etc.) on the catalytic outcome of the complexes. Overall, this review shows that the selectivity and activity of the catalyst may be tuned efficiently through directed modification of the P,O chelator.

Graphical abstract: Structure–reactivity relationships in SHOP-type complexes: tunable catalysts for the oligomerisation and polymerisation of ethylene

Article information

Article type
Perspective
Submitted
19 Oct 2006
Accepted
27 Nov 2006
First published
05 Jan 2007

Dalton Trans., 2007, 515-528

Structure–reactivity relationships in SHOP-type complexes: tunable catalysts for the oligomerisation and polymerisation of ethylene

P. Kuhn, D. Sémeril, D. Matt, M. J. Chetcuti and P. Lutz, Dalton Trans., 2007, 515 DOI: 10.1039/B615259G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements