Cargando…

A broadly tunable synthesis of linear α-olefins

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 c...

Descripción completa

Detalles Bibliográficos
Autores principales: Gollwitzer, Andreas, Dietel, Thomas, Kretschmer, Winfried P., Kempe, Rhett
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663737/
https://www.ncbi.nlm.nih.gov/pubmed/29089510
http://dx.doi.org/10.1038/s41467-017-01507-2
_version_ 1783274869568307200
author Gollwitzer, Andreas
Dietel, Thomas
Kretschmer, Winfried P.
Kempe, Rhett
author_facet Gollwitzer, Andreas
Dietel, Thomas
Kretschmer, Winfried P.
Kempe, Rhett
author_sort Gollwitzer, Andreas
collection PubMed
description 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.
format Online
Article
Text
id pubmed-5663737
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-56637372017-11-02 A broadly tunable synthesis of linear α-olefins Gollwitzer, Andreas Dietel, Thomas Kretschmer, Winfried P. Kempe, Rhett Nat Commun Article 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. Nature Publishing Group UK 2017-10-31 /pmc/articles/PMC5663737/ /pubmed/29089510 http://dx.doi.org/10.1038/s41467-017-01507-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gollwitzer, Andreas
Dietel, Thomas
Kretschmer, Winfried P.
Kempe, Rhett
A broadly tunable synthesis of linear α-olefins
title A broadly tunable synthesis of linear α-olefins
title_full A broadly tunable synthesis of linear α-olefins
title_fullStr A broadly tunable synthesis of linear α-olefins
title_full_unstemmed A broadly tunable synthesis of linear α-olefins
title_short A broadly tunable synthesis of linear α-olefins
title_sort broadly tunable synthesis of linear α-olefins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663737/
https://www.ncbi.nlm.nih.gov/pubmed/29089510
http://dx.doi.org/10.1038/s41467-017-01507-2
work_keys_str_mv AT gollwitzerandreas abroadlytunablesynthesisoflinearaolefins
AT dietelthomas abroadlytunablesynthesisoflinearaolefins
AT kretschmerwinfriedp abroadlytunablesynthesisoflinearaolefins
AT kemperhett abroadlytunablesynthesisoflinearaolefins
AT gollwitzerandreas broadlytunablesynthesisoflinearaolefins
AT dietelthomas broadlytunablesynthesisoflinearaolefins
AT kretschmerwinfriedp broadlytunablesynthesisoflinearaolefins
AT kemperhett broadlytunablesynthesisoflinearaolefins