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A broadly tunable synthesis of linear α-olefins

Author

Listed:
  • Andreas Gollwitzer

    (Universitätsstr. 30, Universität Bayreuth)

  • Thomas Dietel

    (Universitätsstr. 30, Universität Bayreuth)

  • Winfried P. Kretschmer

    (Universitätsstr. 30, Universität Bayreuth)

  • Rhett Kempe

    (Universitätsstr. 30, Universität Bayreuth)

Abstract

The catalytic synthesis of linear α-olefins from ethylene is a technologically highly important reaction. A synthesis concept allowing the formation of selective products and various linear α-olefin product distributions with one catalyst system is highly desirable. Here, we describe a trimetallic catalyst system (Y–Al–Ni) consisting of a rare earth metal polymerization catalyst which can mediate coordinative chain transfer to triethylaluminum combined with a simultaneously operating nickel β-hydride elimination/transfer catalyst. This nickel catalyst displaces the grown alkyl chains forming linear α-olefins and recycles the aluminum-based chain transfer agent. With one catalyst system, we can synthesize product spectra ranging from selective 1-butene formation to α-olefin distributions centered at 850 gmol−1 with a low polydispersity. The key to this highly flexible linear α-olefin synthesis is the easy tuning of the rates of the Y and Ni catalysis independently of each other. The reaction is substoichiometric or formally catalytic regarding the chain transfer agent.

Suggested Citation

  • Andreas Gollwitzer & Thomas Dietel & Winfried P. Kretschmer & Rhett Kempe, 2017. "A broadly tunable synthesis of linear α-olefins," Nature Communications, Nature, vol. 8(1), pages 1-6, December.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-01507-2
    DOI: 10.1038/s41467-017-01507-2
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    Cited by:

    1. Zhongling Li & Wenlong Wu & Menglin Wang & Yanan Wang & Xinlong Ma & Lei Luo & Yue Chen & Kaiyuan Fan & Yang Pan & Hongliang Li & Jie Zeng, 2022. "Ambient-pressure hydrogenation of CO2 into long-chain olefins," Nature Communications, Nature, vol. 13(1), pages 1-10, December.

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