Issue 17, 2017

Ethylene polymerization catalyzed by bridging Ni/Zn heterobimetallics

Abstract

The effect of proximal Zn halides on Ni-catalyzed ethylene polymerization is reported in this work. A series of (NON)NiLX (NON = 2,6-bis-((2,6-diisopropylphenyl)imino)methyl phenoxide; LX = methallyl or L = py, X = tolyl, 2–4) ethylene polymerization precatalysts have been synthesized, as well as a heterobimetallic Ni/Zn complex, (NON)Ni(C4H7)ZnBr2 (5). Each precatalyst could be activated (or promoted) by ZnX2 (X = Cl, Br, Et) to polymerize ethylene. In situ recruitment of ZnX2 by the free imine binding pocket of the NON complexes results in the generation of heterobimetallic active species that produce lower Mn polyethylene than monometallic controls. Room temperature ZnX2-promoted polymerizations with these catalysts resulted in bimodal Mn distributions that result from different catalyst speciation: “dangling” imine-ligated ZnX2 species yield higher Mn polymer while N,O-chelated ZnX2 species yield lower Mn polymer. Running polymerizations at higher temperature yields in only lower Mn polymer resulting from exclusive formation of the thermodynamically favored N,O chelated Ni/Zn heterobimetallic. DFT calculations indicate that this bridging bimetallic complex undergoes β-H elimination more facilely than monometallic Ni analogues, resulting in lower molecular weight polymers.

Graphical abstract: Ethylene polymerization catalyzed by bridging Ni/Zn heterobimetallics

Supplementary files

Article information

Article type
Communication
Submitted
18 jan 2017
Accepted
13 mrt 2017
First published
13 mrt 2017

Dalton Trans., 2017,46, 5513-5517

Ethylene polymerization catalyzed by bridging Ni/Zn heterobimetallics

H. Chiu, A. Koley, P. L. Dunn, R. J. Hue and I. A. Tonks, Dalton Trans., 2017, 46, 5513 DOI: 10.1039/C7DT00222J

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