Catalyst
US-2015344595-A1 · Dec 3, 2015 · US
US9828403B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9828403-B2 |
| Application number | US-201515037483-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 12, 2015 |
| Priority date | Aug 12, 2014 |
| Publication date | Nov 28, 2017 |
| Grant date | Nov 28, 2017 |
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The present invention relates to a transition metal compound that may exhibit high activity in olefin polymerization, and easily control the properties of synthesized olefin polymer such as a chemical structure, molecular weight distribution, a mechanical property, and the like, a catalyst composition comprising the same, and a method for olefin polymerization using the catalyst composition.
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The invention claimed is: 1. A transition metal compound represented by the following Chemical Formula 1: in the Chemical Formula 1, R 1 to R 12 are independently selected from the group consisting of hydrogen, a C1-20 alkyl group, a C2-20 alkenyl group, a C1-20 alkylsilyl group, a C1-20 silylalkyl group, a C1-20 alkoxysilyl group, a C1-20 ether group, a C1-20 silylether group, a C1-20 alkoxy group, a C6-20 aryl group, a C7-20 alkylaryl group and a C7-20 arylalkyl group, or two or more neighboring groups of R 1 to R 12 are optionally connected with each other to form a substituted or unsubstituted aliphatic or aromatic ring, Q 1 and Q 2 are independently hydrogen, halogen, a C1-20 alkyl group, a C2-20 alkenyl group, a C1-20 alkoxy group, a C6-20 aryl group, a C2-20 alkoxyalkyl group, a C3-20 heterocycloalkyl group, a C5-20 heteroaryl group, 1-tert-butoxyhexyl, or pivalate, M is Group 4 transition metal, Xs are independently halogen, a C1-20 alkyl group, a C2-20 alkenyl group, a C6-20 aryl group, a nitro group, an amido group, a C1-20 alkylsilyl group, a C1-20 alkoxy group or a C1-20 sulfonate group, and n is an integer of 1 to 10. 2. The transition metal compound according to claim 1 , wherein M is selected from the group consisting of Ti, Zr and Hf. 3. The transition metal compound according to claim 1 , wherein R 1 is a C1-20 alkyl group, a C1-20 alkoxyl group, or a C6-20 aryl group. 4. The transition metal compound according to claim 1 , wherein R 8 is a C1-20 alkyl group, a C1-20 alkoxy group, a C1-20 alkylsilyl group, a C1-20 silylalkyl group, a C6-20 aryl group, or a C7-20 alkylaryl group. 5. The transition metal compound according to claim 1 , wherein Q 1 and Q 2 are independently a C1-20 alkyl group, a C1-20 alkenyl group, a C1-20 alkoxy group, or a C6-20 aryl group. 6. A catalyst composition comprising the transition metal compound represented by the Chemical Formula 1 according to claim 1 ; and a cocatalyst comprising at least one selected from the group consisting of the following Chemical Formulae 2 to 4: [L-H] + [Z(E) 4 ] − or [L] + [Z(E) 4 ] − [Chemical Formula 2] in the Chemical Formula 2, L is neutral or cationic Lewis base, [L-H] + or [L] + is Bronsted acid, H is a hydrogen atom, Z is Group 13 element, Es are independently halogen with hydrogen valence number of 1 or more, a C1-20 hydrocarbyl, a C6-20 aryl group or a C1-20 alkyl group unsubstituted or substituted with alkoxy or phenoxy, D(R 13 ) 3 [Chemical Formula 3] in the Chemical Formula 3, D is aluminum or boron, R 13 s are independently halogen; a C1-20 hydrocarbyl group; or a C1-20 hydrocarbyl group substituted with halogen, in the Chemical Formula 4, R 14 , R 15 and R 16 are independently hydrogen; halogen; a C1-20 hydrocarbyl group; or a C1-20 hydrocarbyl group substituted with halogen, and a is an integer of 2 or more. 7. The catalyst composition according to claim 6 , further comprising a solvent. 8. The catalyst composition according to claim 6 , wherein the transition metal compound and the cocatalyst are supported in a carrier. 9. A method for preparing an olefin polymer, comprising a step of polymerizing olefin monomers in the presence of the catalyst composition according to claim 6 . 10. The method according to claim 9 , wherein the olefin monomer includes at least one selected from the group consisting of ethylene, propylene, 1-butene, 1-penten, 4-methyl-1-penten, 1-hexene, 1-heptene, 1-octene, 1-decene, 1-undecene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-eicosene, norbornene, norbornadiene, ethylidene norbornene, phenyl norbornene, vinyl norbornene, dicylcopentadiene, 1,4-butadiene, 1,5-pentadiene, 1,6-hexadiene, styrene, alpha-methylstyrene, divinylbenzene and 3-chloromethylstyrene.
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