Catalyst composition and method of preparing polymer including the same
US-2015361196-A1 · Dec 17, 2015 · US
US10093755B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10093755-B2 |
| Application number | US-201515323595-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 24, 2015 |
| Priority date | Nov 13, 2014 |
| Publication date | Oct 9, 2018 |
| Grant date | Oct 9, 2018 |
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The present invention relates to a novel ligand compound, a transition metal compound and a catalyst composition including the transition metal compound. The novel ligand compound and the transition metal compound of the present invention may be usefully used as the catalyst of a polymerization reaction for preparing an olefin polymer having a low density relative to a CGC catalyst. In addition, a product having a low melt index (MI) and a high molecular weight may be manufactured using the olefin polymer polymerized using the catalyst composition including the transition metal compound.
Opening claim text (preview).
The invention claimed is: 1. A transition metal compound represented by the following Formula 1: in the above Formula 1, R 1 to R 6 are each independently hydrogen; alkyl having 1 to 20 carbon atoms; alkenyl having 2 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; alkylaryl having 7 to 20 carbon atoms; or arylalkyl having 7 to 20 carbon atoms, R 7 and R 8 are each independently hydrogen; alkyl having 1 to 20 carbon atoms; alkenyl having 2 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; alkylaryl having 6 to 20 carbon atoms; arylalkyl having 7 to 20 carbon atoms; alkyl amido having 1 to 20 carbon atoms; aryl amido having 6 to 20 carbon atoms; or alkylidene having 1 to 20 carbon atoms, R 9 is hydrogen; alkyl having 1 to 20 carbon atoms; alkenyl having 2 to 20 carbon atoms; alkoxy having 1 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; arylalkoxy having 7 to 20 carbon atoms; alkylaryl having 7 to 20 carbon atoms; or arylalkyl having 7 to 20 carbon atoms, at least two adjacent elements of R 1 to R 9 are optionally connected to each other to form a ring, R 10 and R 11 are each independently hydrogen, halogen, alkyl having 1 to 20 carbon atoms, alkenyl having 2 to 20 carbon atoms, aryl having 6 to 20 carbon atoms, alkylaryl having 7 to 20 carbon atoms; arylalkyl having 7 to 20 carbon atoms, alkylamino having 1 to 20 carbon atoms, arylamino having 6 to 20 carbon atoms, or alkylidene having 1 to 20 carbon atoms, Q is Si, C, N, P, or S, and M is a transition metal in group 4. 2. The transition metal compound of claim 1 , wherein in the above Formula 1, R 1 to R 6 are each independently hydrogen; alkyl having 1 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; alkylaryl having 7 to 20 carbon atoms; or arylalkyl having 7 to 20 carbon atoms, R 7 and R 8 are each independently hydrogen; alkyl having 1 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; or alkylaryl having 6 to 20 carbon atoms, R 9 is hydrogen; alkyl having 1 to 20 carbon atoms; alkoxy having 1 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; arylalkoxy having 7 to 20 carbon atoms; alkylaryl having 7 to 20 carbon atoms; or arylalkyl having 7 to 20 carbon atoms, at least two adjacent elements of R 1 to R 9 are optionally connected to each other to form an aliphatic ring having 5 to 20 carbon atoms or an aromatic ring having 6 to 20 carbon atoms, the aliphatic ring or the aromatic ring being substituted with halogen, alkyl having 1 to 20 carbon atoms, alkenyl having 2 to 20 carbon atoms, or aryl having 6 to 20 carbon atoms, and Q is Si, C, N, or P. 3. The transition metal compound of claim 2 , wherein in the above Formula 1, R 1 to R 6 are each independently hydrogen; alkyl having 1 to 20 carbon atoms; or aryl having 6 to 20 carbon atoms, R 7 and R 8 are each independently hydrogen; alkyl having 1 to 20 carbon atoms; or aryl having 6 to 20 carbon atoms, R 9 is alkyl having 1 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; arylalkoxy having 7 to 20 carbon atoms; or arylalkyl having 7 to 20 carbon atoms, and Q is Si. 4. The transition metal compound of claim 1 , wherein M is Ti, Hf, or Zr. 5. The transition metal compound of claim 4 , wherein the compound represented by Formula 1 is represented by one of the following formulae: 6. A method of preparing a transition metal compound of Formula 1 by reacting a compound represented by the following Formula 2 with a compound represented by the following Formula 7 and an organolithium compound: in the above formulae, R 1 to R 6 are each independently hydrogen; alkyl having 1 to 20 carbon atoms; alkenyl having 2 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; alkylaryl having 7 to 20 carbon atoms; or arylalkyl having 7 to 20 carbon atoms, R 7 and R 8 are each independently hydrogen; alkyl having 1 to 20 carbon atoms; alkenyl having 2 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; alkylaryl having 6 to 20 carbon atoms; arylalkyl having 7 to 20 carbon atoms; alkyl amido having 1 to 20 carbon atoms; aryl amido having 6 to 20 carbon atoms; or alkylidene having 1 to 20 carbon atoms, R 9 is hydrogen; alkyl having 1 to 20 carbon atoms; alkenyl having 2 to 20 carbon atoms; alkoxy having 1 to 20 carbon atoms; aryl having 6 to 20 carbon atoms; arylalkoxy having 7 to 20 carbon atoms; alkylaryl having 7 to 20 carbon atoms; or arylalkyl having 7 to 20 carbon atoms, at least two adjacent elements of R 1 to R 9 are optionally connected to each other to form a ring, R 10 and R 11 are each independently hydrogen, halogen, alkyl having 1 to 20 carbon atoms, alkenyl having 2 to 20 carbon atoms, aryl having 6 to 20 carbon atoms, alkylaryl having 7 to 20 carbon atoms, arylalkyl having 7 to 20 carbon atoms, alkylamino having 1 to 20 carbon atoms, arylamino having 6 to 20 carbon atoms, or alkylidene having 1 to 20 carbon atoms, Q is Si, C, N, P, or S, and M is a transition metal in group 7. 7. A catalyst composition comprising the transition metal compound according to claim 1 . 8. The catalyst composition of claim 7 , further comprising at least one co-catalyst. 9. The catalyst composition of claim 8 , wherein the co-catalyst comprises at least one selected from the following Formulae 8 to 10: —[Al(R 22 )—O] a — [Formula 8] in the above formula, each R 22 is independently a halogen radical; a hydrocarbyl radical having 1 to 20 carbon atoms; or a hydrocarbyl radical having 1 to 20 carbon atoms, the hydrocarbyl radical being substituted with halogen; and a is an integer of 2 or more; D(R 22 ) 3 [Formula 9] in the above formula, D is aluminum or boron; and each R 22 is the same as defined above; [L-H] + [Z(A) 4 ] − or [L] + [Z(A) 4 ] − [Formula 10] in the above formula, L is a neutral or a cationic Lewis acid; H is a hydrogen atom; Z is an element in group 13; each A is independently aryl having 6 to 20 carbon atoms or alkyl having 1 to 20 carbon atoms, where at least one hydrogen atom is independently optionally substituted with a substituent; and the substituent is halogen, hydrocarbyl having 1 to 20 carbon atoms, alkoxy having 1 to 20 carbon atoms or aryloxy having 6 to 20 carbon atoms. 10. The catalyst composition of claim 8 , further comprising a reaction solvent. 11. A method of preparing a polymer in the presence of the catalyst composition according to claim 7 . 12. The method of preparing a polymer of claim 11 , wherein the polymer is a homopolymer or a copolymer of polyolefin.
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