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.

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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
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article

Synthesis and Evaluation of Trialkyl Ammonium Tetrakis(perfluorophenyl) Aluminate, a Highly Efficient Activator for High-Temperature Ethylene-α-Olefin Copolymerization Reactions

Robert Bellair, Sean Bremer, Jerzy Klosin, Todd D. Senecal et al.
1 citations
Organometallics
Organometallic Complex Synthesis and Catalysis
0.25
article

Synthesis and Evaluation of Trialkyl Ammonium Tetrakis(perfluorophenyl) Aluminate, a Highly Efficient Activator for High-Temperature Ethylene-α-Olefin Copolymerization Reactions

Robert Bellair, Sean Bremer, Jerzy Klosin, Todd D. Senecal, Travis W. Scholtz
article en
1 citations

Abstract

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.

OrganometallicsVol. 43(20)
Dow Chemical (United States) (US)
Openalex Percentile: Top 48%
Organometallic Complex Synthesis and Catalysis
0.25
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