Ligand compound, transition metal compound, and catalyst composition including the same

US11274113B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11274113-B2
Application numberUS-201916643205-A
CountryUS
Kind codeB2
Filing dateJan 11, 2019
Priority dateJan 12, 2018
Publication dateMar 15, 2022
Grant dateMar 15, 2022

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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The present invention provides a novel ligand compound, a transition metal compound and a catalyst composition including the same.

First claim

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The invention claimed is: 1. A transition metal compound represented by the following Formula 1: X is O, S or a single bond; M is a transition metal in group 4; Q 1 and Q 2 are each independently hydrogen; a halogen group; an alkyl group of 1 to 20 carbon atoms; a cycloalkyl group of 3 to 20 carbon atoms; an alkenyl group of 2 to 20 carbon atoms; an aryl group of 6 to 20 carbon atoms; an alkylaryl group of 7 to 20 carbon atoms; an arylalkyl group of 7 to 20 carbon atoms; an alkylamino group of 1 to 20 carbon atoms; or an arylamino group of 6 to 20 carbon atoms, R 1 to R 4 are each independently hydrogen; a silyl group; an alkyl group of 1 to 20 carbon atoms; an alkenyl group of 2 to 20 carbon atoms; a cycloalkyl group of 3 to 20 carbon atoms; an aryl group of 6 to 20 carbon atoms; an alkylaryl group of 7 to 20 carbon atoms; an arylalkyl group of 7 to 20 carbon atoms; or a metalloid radical of a metal in group 14, which is substituted with a hydrocarbyl group of 1 to 20 carbon atoms, where adjacent two or more among R 1 to R 4 are optionally connected with each other to form an aliphatic ring of 3 to 20 carbon atoms, an aromatic ring of 6 to 20 carbon atoms or a heteroaromatic ring of 4 to 20 carbon atoms, provided that when X is a single bond, adjacent two or more among R 1 to R 4 are connected with each other to form a heteroaromatic ring of 4 to 20 carbon atoms; and R 5 to R 11 are each independently hydrogen; a silyl group; a halogen group; an alkyl group of 1 to 20 carbon atoms; an alkenyl group of 2 to 20 carbon atoms; a cycloalkyl group of 3 to 20 carbon atoms; an aryl group of 6 to 20 carbon atoms; an arylalkyl group of 7 to 20 carbon atoms; an alkylaryl group of 7 to 20 carbon atoms; an alkoxy group of 1 to 20 carbon atoms; or an aryloxy group of 6 to 20 carbon atoms; where adjacent two or more among R 5 to R 11 are optionally connected with each other to form an aliphatic ring of 3 to 20 carbon atoms, or an aromatic ring of 6 to 20 carbon atoms. 2. The transition metal compound according to claim 1 , wherein X is O, S or a single bond, M is a transition metal in group 4, Q 1 and Q 2 are each independently hydrogen or an alkyl group of 1 to 12 carbon atoms, R 1 to R 4 are each independently hydrogen, an alkyl group of 1 to 12 carbon atoms or an aryl group of 6 to 12 carbon atoms, where adjacent two or more among Ru to R4 are optionally connected with each other to form an aliphatic ring of 3 to 20 carbon atoms, an aromatic ring of 6 to 20 carbon atoms or a heteroaromatic ring of 4 to 20 carbon atoms, provided that when X is a single bond, adjacent two or more among R 1 to R 4 are connected with each other to form a heteroaromatic ring of 4 to 20 carbon atoms, and R 5 to R 11 are each independently hydrogen, an alkyl group of 1 to 12 carbon atoms or an aryl group of 6 to 12 carbon atoms. 3. The transition metal compound according to claim 1 , wherein X is O, or S, M is a transition metal in group 4, Q 1 and Q 2 are each independently hydrogen or an alkyl group of 1 to 12 carbon atoms, and R 1 to R 11 are each independently hydrogen, an alkyl group of 1 to 12 carbon atoms or an aryl group of 6 to 12 carbon atoms. 4. The transition metal compound according to claim 1 , wherein the transition metal compound is represented by the following Formula 1-1: in Formula 1-1, X is O, S or a single bond, M is a transition metal in group 4, Q 1 and Q 2 are each independently hydrogen or an alkyl group of 1 to 12 carbon atoms, and R 1 , R 2 and R 5 to R 13 are each independently hydrogen, an alkyl group of 1 to 12 carbon atoms or an aryl group of 6 to 12 carbon atoms, where R 12 and R 13 are optionally connected with each other to form an aliphatic ring of 3 to 18 carbon atoms or an aromatic ring of 6 to 18 carbon atoms, and the aliphatic ring or the aromatic ring is optionally substituted with a halogen group, an alkyl group of 1 to 12 carbon atoms, an alkenyl group of 2 to 12 carbon atoms, or an aryl group of 6 to 12 carbon atoms. 5. The transition metal compound according to claim 1 , wherein X is a single bond, M is a transition metal in group 4, Q 1 and Q 2 are each independently hydrogen or an alkyl group of 1 to 12 carbon atoms, R 1 to R 4 are each independently hydrogen, an alkyl group of 1 to 12 carbon atoms or an aryl group of 6 to 12 carbon atoms, where adjacent two or more among R 1 to R 4 are optionally connected with each other to form an aliphatic ring of 3 to 20 carbon atoms, an aromatic ring of 6 to 20 carbon atoms or a heteroaromatic ring of 4 to 20 carbon atoms, provided that when X is a single bond, adjacent two or more among R 1 to R 4 are connected with each other to form a heteroaromatic ring of 4 to 20 carbon atoms, and R 5 to R 11 are each independently hydrogen, an alkyl group of 1 to 12 carbon atoms or an aryl group of 6 to 12 carbon atoms. 6. The transition metal compound according to claim 1 , wherein X is O or S, M is a transition metal in group 4, Q 1 and Q 2 are each independently hydrogen or an alkyl group of 1 to 12 carbon atoms, R 1 to R 4 are each independently hydrogen, an alkyl group of 1 to 12 carbon atoms or an aryl group of 6 to 12 carbon atoms, where adjacent two or more among R 1 to R 4 are optionally connected with each other to form an aliphatic ring of 3 to 20 carbon atoms, an aromatic ring of 6 to 20 carbon atoms or a heteroaromatic ring of 4 to 20 carbon atoms, and R 5 to R 11 are each independently hydrogen, an alkyl group of 1 to 12 carbon atoms or an aryl group of 6 to 12 carbon atoms. 7. The transition metal compound according to claim 1 , wherein the transition metal compound is selected from the group consisting of the following structures: 8. A catalyst composition for preparing polyolefin, the catalyst composition comprising the transition metal compound according to claim 1 . 9. The catalyst composition according to claim 8 , further comprising one or more kinds of cocatalysts. 10. The catalyst composition according to claim 9 , wherein the cocatalyst comprises one or more compounds selected from the following Formulae 4 to 6: —[Al(R 12 )—O] a —  [Formula 4] where each R 12 is independently a halogen group; a hydrocarbyl group of 1 to 20 carbon atoms; or a halogen-substituted hydrocarbyl group of 1 to 20 carbon atoms; and a is an integer of 2 or more; D(R 13 ) 3   [Formula 5] where D is aluminum or boron; and each R 13 is independently a halogen group; a hydrocarbyl group of 1 to 20 carbon atoms; or a halogen-substituted hydrocarbyl group of 1 to 20 carbon atoms; [L—H] + [Z(A) 4 ] − or [L] + [Z(A) 4 ] −   [Formula 6] where L is a neutral or a cationic Lewis acid; H is a hydrogen atom; Z is an element in group 13; and each A is independently an aryl group of 6 to 20 carbon atoms or an alkyl group of 1 to 20 carbon atoms, where one or more hydrogen atoms are optionally substituted with a substituent; wherein the substituent is a halogen group, a hydrocarbyl group of 1 to 20 carbon atoms, an alkoxy group of 1 to 20 carbon atoms, or an aryloxy group of 6 to 20 carbon atoms. 11. A method of preparing polyolefin, comprising contacting an olefin monomer with a catalyst composition according to claim 8 . 12. The method of preparing polyolefin ac

Assignees

Inventors

Classifications

  • directly linked by a ring-member-to-ring-member bond · CPC title

  • directly linked by a ring-member-to-ring-member bond · CPC title

  • directly linked by a ring-member-to-ring-member bond · CPC title

  • [b, e]-condensed with two six-membered rings · CPC title

  • with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system · CPC title

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What does patent US11274113B2 cover?
The present invention provides a novel ligand compound, a transition metal compound and a catalyst composition including the same.
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C07F17/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Mar 15 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).