Title data
Lukas, Fabian ; Simon, Paula A. ; Dietel, Thomas ; Kretschmer, Winfried ; Kempe, Rhett:
Synthesis of Branched α-Olefins via Trimerization and Tetramerization of Ethylene.
In: Advanced Science.
(August 2024)
.
- 2405653.
ISSN 2198-3844
DOI: https://doi.org/10.1002/advs.202405653
Abstract in another language
α-Olefins are very important bulk and fine chemicals and their synthesis from ethylene, an abundantly available and inexpensive feedstock, is highly attractive. Unfortunately, the direct or on-purpose synthesis of olefins from ethylene is limited to three examples, 1-butene, 1-hexene, and 1-octene, all having a linear structure. Herein, the direct synthesis of 3-methylenepentane and 4-ethylhex-1-ene, branched trimerization, and tetramerization products of ethylene, respectively, is reported. Different molecular titanium catalysts, all highly active, with a selectivity toward the formation of the branched ethylene trimer or tetramer, the employment of different activators, and different reaction conditions are the key to selective product formation. The long-time stability of selected catalysts employed permits upscaling as demonstrated for the synthesis of 4-ethylhex-1-ene (52 g isolated, TON(ethylene) 10.7 · 106).
Further data
Item Type: | Article in a journal |
---|---|
Refereed: | Yes |
Institutions of the University: | Faculties > Faculty of Biology, Chemistry and Earth Sciences Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Inorganic Chemistry II Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Inorganic Chemistry II > Chair Inorganic Chemistry II - Univ.-Prof. Dr. Rhett Kempe |
Result of work at the UBT: | Yes |
DDC Subjects: | 500 Science 500 Science > 540 Chemistry |
Date Deposited: | 14 Aug 2024 05:35 |
Last Modified: | 14 Aug 2024 06:35 |
URI: | https://eref.uni-bayreuth.de/id/eprint/90190 |