Synthesis and Evaluation of Trialkyl Ammonium Tetrakis(perfluorophenyl) Aluminate, a Highly Efficient Activator for High-Temperature Ethylene-α-Olefin Copolymerization Reactions
The new salt, [HNMe(C18H37)2][Al(C6F5)4], was prepared and was shown to be highly effective as an activator for Group IV precatalysts in high-temperature ethylene-1-octene copolymerization reactions. The performance of this activator closely mirrors that of the state-of-the-art activator borate-based analogue. Unlike the borate analogue, the aluminate activator reacts readily with water at ambient temperature, generating pentafluorobenzene, the only fluorine-containing product. Such a feature might be helpful when preparing polymers without any charged contaminants. Unlike some of the other aluminum compounds containing perfluorophenyl groups, [HNMe(C18H37)2][Al(C6F5)4] was found not to be impact-sensitive and is stable at ambient temperature for months. Detailed evaluation of this aluminate salt and several other aluminum alkyls/aryls (e.g., Al(C6F5)3(THF), Al(C6F5)3, AlEt3, and MMAO-3A) was carried out to evaluate their reactive chemistry and safety profiles.
Authors
- Robert Bellair (ORCID: https://orcid.org/0000-0002-4440-6649)
- Sean Bremer
- Jerzy Klosin (ORCID: https://orcid.org/0000-0002-9045-7308)
- Todd D. Senecal (ORCID: https://orcid.org/0000-0002-5673-5538)
- Travis W. Scholtz
Institutions
- Dow Chemical (United States) (US)
Publication Details
- Journal
- Organometallics
- Published
- 2024-09-23
- DOI
- https://doi.org/10.1021/acs.organomet.4c00268
- Citations
- 1
- Primary Topic
- Organometallic Complex Synthesis and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.25