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Recent advances in Ni-mediated ethylene chain growth: Nimine-donor ligand effects on catalytic activity, thermal stability and oligo-/polymer structure

journal contribution
posted on 2017-07-06, 15:02 authored by Zheng Wang, Qingbin Liu, Gregory A. Solan, Wen-Hua Sun
Homogeneous nickel catalysts have a considerable track record for mediating ethylene chain growth in the form of oligomerization and more recently polymerization. Within the polymerization arena, high molecular weight materials incorporating various degrees of branching, anywhere from linear to moderately branched through to hyperbranched, highlight the versatility of this type of catalyst. This review focuses on recent progress related to structural modifications made to the pre-catalyst, and in particular to the multidentate Nimine-ligand manifold, and how these changes impact on thermal stability and activity of the catalyst as well as the microstructural properties of the polyethylene and the distribution of the oligomeric fractions. In addition to ongoing process development directed towards commodity-type polyolefinic materials, the emergence of nickel catalysts that can form elastomeric-type materials from a single ethylene feed, without the addition of a high-cost α-olefin such as 1-hexene or 1-octene, offers considerable opportunities for future commercial applications.

Funding

This work is supported by the National Natural Science Foundation of China (21374123, 21476060, and U1362204). G.A.S. thanks the Chinese Academy of Sciences for a Visiting Scientist Fellowship.

History

Citation

Coordination Chemistry Reviews, 2017

Author affiliation

/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistry

Version

  • AM (Accepted Manuscript)

Published in

Coordination Chemistry Reviews

Publisher

Elsevier

issn

0010-8545

Acceptance date

2017-06-08

Copyright date

2017

Available date

2018-06-10

Publisher version

http://www.sciencedirect.com/science/article/pii/S0010854517302333

Notes

The file associated with this record is under embargo until 12 months after publication, in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above.

Language

en

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