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Published December 6, 2023 | Published
Journal Article Open

Acrylate-Induced β-H Elimination in Coordination Insertion Copolymerizaton Catalyzed by Nickel

Abstract

Polar monomer-induced β-H elimination is a key elementary step in polar polyolefin synthesis by coordination polymerization but remains underexplored. Herein, we show that a bulky neutral Ni catalyst, 1^(Ph), is not only a high-performance catalyst in ethylene/acrylate copolymerization (activity up to ∼37,000 kg/(mol·h) at 130 °C in a batch reactor, mol % tBA ∼ 0.3) but also a suitable platform for investigation of acrylate-induced β-H elimination. 4^(Ph-tBu), a novel Ni alkyl complex generated after acrylate-induced β-H elimination and subsequent acrylate insertion, was identified and characterized by crystallography. A combination of catalysis and mechanistic studies reveals effects of the acrylate monomer, bidentate ligand, and the labile ligand (e.g., pyridine) on the kinetics of β-H elimination, the role of β-H elimination in copolymerization catalysis as a chain-termination pathway, and its potential in controlling the polymer microstructure in polar polyolefin synthesis.

Copyright and License

 © 2023 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0.

Acknowledgement

We are grateful to Dow (TA) for funding. We thank Alex J. Nett and Todd D. Senecal for insightful discussions. We thank Manar M. Shoshani, Linh N.V. Le, Michael Takase, and Matthew R. Espinosa for assistance with X-ray crystallography and David VanderVelde for assistance with NMR spectroscopy. We thank Heidi Clements for assistance in collecting polymer characterization data (GPC, DSC, and FT-IR). Support has been provided for the X-ray diffraction and NMR instrumentation via the Dow Next Generation Educator Fund.

Contributions

The manuscript was written through contributions of all authors.

Conflict of Interest

The authors declare no competing financial interest.

Data Availability

CCDC 2280179–81 contain the supplementary crystallographic data for this paper.

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Additional details

Created:
December 11, 2023
Modified:
December 11, 2023