James E. Radcliffe
Phosphanyl Methanimine (PCN) Ligands for the Selective Trimerization/Tetramerization of Ethylene with Chromium
Radcliffe, James E.; Batsanov, Andrei S.; Smith, David M.; Scott, John A.; Dyer, Philip W.; Hanton, Martin J.
Authors
Andrei S. Batsanov
David M. Smith
John A. Scott
Professor Philip Dyer p.w.dyer@durham.ac.uk
Professor
Martin J. Hanton
Abstract
1-Phosphanyl methanimine ligands, R2P–C(Ph)═NR′, may be prepared via a modular, convergent synthesis in good overall yield. Coordination chemistry studies with chromium confirm that they bind in a bidentate κ2-P,N mode. In combination with chromium and an activator, these ligands promote the selective oligomerization of ethylene to 1-hexene and 1-octene with high activity. Notably, an exceptionally high liquid fraction selectivity to saleable products (1-hexene + 1-octene) is observed (>95%), along with a potent ligand dependence, such that selectivity can be varied from pure trimerization through to mixed trimerisation/tetramerisation with a 1-octene:1-hexene (OTH) ratio of 1.7.
Citation
Radcliffe, J. E., Batsanov, A. S., Smith, D. M., Scott, J. A., Dyer, P. W., & Hanton, M. J. (2015). Phosphanyl Methanimine (PCN) Ligands for the Selective Trimerization/Tetramerization of Ethylene with Chromium. ACS Catalysis, 5(12), 7095-7098. https://doi.org/10.1021/acscatal.5b02106
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 30, 2015 |
Online Publication Date | Nov 2, 2015 |
Publication Date | Dec 4, 2015 |
Deposit Date | Nov 2, 2015 |
Publicly Available Date | Oct 30, 2016 |
Journal | ACS Catalysis |
Electronic ISSN | 2155-5435 |
Publisher | American Chemical Society |
Peer Reviewed | Peer Reviewed |
Volume | 5 |
Issue | 12 |
Pages | 7095-7098 |
DOI | https://doi.org/10.1021/acscatal.5b02106 |
Keywords | Oligomerization, Trimerization, Tetramerization, Ethylene, Catalysis, α-olefins, Chromium, P,N-ligands. |
Public URL | https://durham-repository.worktribe.com/output/1418862 |
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Copyright Statement
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Catalysis, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/acscatal.5b02106.
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