Catalyst compositions that have modified activity and processes to make them
US-2024218100-A1 · Jul 4, 2024 · US
US2022162352A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022162352-A1 |
| Application number | US-202017599095-A |
| Country | US |
| Kind code | A1 |
| Filing date | Mar 24, 2020 |
| Priority date | Mar 28, 2019 |
| Publication date | May 26, 2022 |
| Grant date | — |
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Embodiments include activators having a structure according to formula (I).
Opening claim text (preview).
1 . An activator having a structure according to formula (I): where: M is a metal in a +3 oxidation state, the metal being selected from boron, aluminum, gallium, scandium, yttrium, or a lanthanide; [Cat] + is a cation; R 1 , R 2 , R 3 , R 4 R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are independently chosen from (C 1 -C 40 )alkyl, (C 6 -C 40 )aryl, —H, —NR C 2 , —OR C , —SR C , or halogen, wherein each R C is independently a (C 1 -C 30 )hydrocarbyl or —H, provided at least one of R 1-4 , and one of R 5-8 , and one of R 9-12 , and one of R 13-16 is a fluorine-substituted (C 1 -C 40 )alkyl, a fluorine-substituted (C 6 -C 40 )aryl, or —F; and R 17 and R 18 are (C 1 -C 40 )alkyl, (C 1 -C 40 )heteroalkyl, a fluorine-substituted (C 1 -C 40 )alkyl, or a fluorine-substituted (C 6 -C 40 )aryl. 2 . The activator of claim 1 , wherein R 1 , R 2 , R 3 , R 4 R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are independently (C 1 -C 10 )alkyl, —F, or —H, provided at least one of R 1-4 , and one of R 5-8 , and one of R 9-12 , and one of R 13-16 is a fluorine-substituted (C 1 -C 10 )alkyl or —F. 3 . The activator of claim 1 , wherein R 17 and R 18 are (C 1 -C 10 )alkyl. 4 . The activator of claim 1 wherein [Cat + ] is a protonated tertiary amine. 5 . The activator of claim 1 , wherein [Cat] + is + N(H)R N 3 , wherein each R N is independently (C 1 -C 20 )alkyl. 6 . The activator of claim 1 , wherein: at least one of R 1 , R 2 , R 3 , and R 4 is —F or fluoroalkyl; at least one of R 5 , R 6 , R 7 , and R 8 is —F or fluoroalkyl; at least one of R 9 , R 10 , R 11 , and R 12 is —F or fluoroalkyl; and at least one of R 13 , R 14 , R 15 , and R 16 is —F or fluoroalkyl. 7 . The activator of claim 1 , wherein: at least two of R 1 , R 2 , R 3 , and R 4 are —F or fluoroalkyl; at least two of R 5 , R 6 , R 7 , and R 8 are —F or fluoroalkyl; at least two of R 9 , R 10 , R 11 , and R 12 are —F or fluoroalkyl; and at least two of R 13 , R 14 , R 15 , and R 16 are —F or fluoroalkyl. 8 . The activator of claim 1 , wherein: at least three of R 1 , R 2 , R 3 , and R 4 are —F or fluoroalkyl; at least three of R 5 , R 6 , R 7 , and R 8 are —F or fluoroalkyl; at least three of R 9 , R 10 , R 11 , and R 12 are —F or fluoroalkyl; and at least three of R 13 , R 14 , R 15 , and R 16 are —F or fluoroalkyl. 9 . The activator of claim 1 , wherein: at least four of R 1 , R 2 , R 3 , and R 4 are —F or fluoroalkyl; at least four of R 5 , R 6 , R 7 , and R 8 are —F or fluoroalkyl; at least four of R 9 , R 10 , R 11 , and R 12 are —F or fluoroalkyl; and at least four of R 13 , R 14 , R 15 , and R 16 are —F or fluoroalkyl. 10 . A catalyst system comprising an activator of claim 1 and a procatalyst, wherein the procatalyst is rendered catalytically active by contacting the procatalyst to the activator. 11 . A process for polymerizing olefins, the process comprising contacting ethylene and optionally a (C 3 -C 40 )α-olefin in the presences of a catalysts system according to claim 10 .
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