US10385146B2ActiveUtilityA1
Metallocene compound
Est. expiryJun 5, 2035(~8.9 yrs left)· nominal 20-yr term from priority
C07F 7/0803C07F 7/00C07F 7/30C08F 4/61927C08F 210/16C07F 7/003C07F 17/00C07F 7/02C08F 10/02C08F 4/65912C08F 110/02C08F 2420/07C08F 2420/10
42
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References
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Claims
Abstract
The present disclosure relates to a novel metallocene compound. The metallocene compound according to the present disclosure may be used for the preparation of an olefin-based polymer, may have excellent ability, and may produce an olefin-based polymer having a relatively high molecular weight compared with the case of using a catalyst composition having a similar structure due to the structural and electrical steric hindrance effect.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. A metallocene compound having the following Chemical Formula 1:
wherein in Chemical Formula 1,
M is a Group 4 transition metal;
B 1 is carbon, silicon, or germanium;
Q 1 and Q 2 are the same as or different from each other, and are each independently hydrogen, halogen, a C1 to C20 alkyl group, a C2 to C20 alkenyl group, a C6 to C20 aryl group, a C7 to C20 alkylaryl group, a C7 to C20 arylalkyl group, a C1 to C20 alkoxy group, a C2 to C20 alkoxyalkyl group, a C3 to C20 heterocycloalkyl group, or a C5 to C20 heteroaryl group;
X 1 and X 2 are the same as or different from each other, and are each independently halogen, a C1 to C20 alkyl group, a C2 to C20 alkenyl group, a C6 to C20 aryl group, a nitro group, an amido group, a C1 to C20 alkylsilyl group, a C1 to C20 alkoxy group, or a C1 to C20 sulfonate group;
C 1 has the following Chemical Formula 2a, and C 2 has any one of the following Chemical Formula 2b, Chemical Formula 2c, Chemical Formula 2d, and Chemical Formula 2e;
wherein, in Chemical Formulae 2a, 2b, 2c, 2d, and 2e,
B 2 is a single bond or a C1 to C3 alkylene group,
* is a site to which M or B1 of Chemical Formula 1 is connected,
R 1 to R 5 are the same as or different from each other, and are each independently hydrogen, halogen, a C1 to C20 alkyl group, a C2 to C20 alkenyl group, an C1 to C20 ether group, a C1 to C20 alkoxy group, a C6 to C20 aryl group, a C7 to C20 alkylaryl group, or a C7 to C20 arylalkyl group,
R 6 to R 32 are the same as or different from each other, and are each independently hydrogen, halogen, a C1 to C20 alkyl group, a C1 to C20 alkoxy group, a C6 to C20 aryl group, a C7 to C20 alkylaryl group, or a C7 to C20 arylalkyl group,
R′ 1 to R′ 3 are the same as or different from each other, and are each independently hydrogen, halogen, or a C1 to C20 alkyl group.
2. A method of preparing an ethylene copolymer using the metallocene compound of claim 1 .
3. The metallocene compound of claim 1 , wherein R 1 to R 5 in the Chemical Formulae 2a, 2b, 2c, 2d, and 2e are each independently hydrogen, halogen, a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, an ethylene group, a propylene group, a butylene group, a phenyl group, a benzyl group, a naphthyl group, a halogen group, an ether group, a dimethyl ether group, a methoxy group, an ethoxy group, or a tert-butoxyhexyl group, and
R 6 to R 22 and R 24 to R 32 are each independently hydrogen, halogen, a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, an ethylene group, a propylene group, a butylene group, a phenyl group, a benzyl group, a naphthyl group, a halogen group, an ether group, a trimethylsilyl group, a triethylsilyl group, a tripropylsilyl group, a tributylsilyl group, a triisopropylsilyl group, a trimethylsilylmethyl group, a dimethyl ether group, tert-butyldimethylsilyl ether group, a methoxy group, an ethoxy group, or a tert-butoxyhexyl group.
4. A method of preparing an ethylene copolymer using the metallocene compound of claim 3 .
5. The metallocene compound of claim 1 , wherein Q 1 and Q 2 in the Chemical Formula 1 are each independently hydrogen, a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, a tert-butyl group, a methoxymethyl group, a tert-butoxymethyl group, a 1-ethoxyethyl group, a 1-methyl-1-methoxyethyl group, a tert-butoxyhexyl group, a tetrahydropyranyl group, or a tetrahydrofuranyl group.
6. A method of preparing an ethylene copolymer using the metallocene compound of claim 5 .
7. The metallocene compound of claim 1 , wherein the compound of Chemical Formula 2a is any one of the following structural formulae:
8. A method of preparing an ethylene copolymer using the metallocene compound of claim 7 .
9. The metallocene compound of claim 1 , wherein the compound of Chemical Formula 2b is any one of the following structural formulae:
10. A method of preparing an ethylene copolymer using the metallocene compound of claim 9 .
11. The metallocene compound of claim 1 , wherein the compound of Chemical Formula 2c is any one of the following structural formulae:
12. A method of preparing an ethylene copolymer using the metallocene compound of claim 11 .
13. The metallocene compound of claim 1 , wherein the compound of Chemical Formula 2d is any one of the following structural formulae:
14. A method of preparing an ethylene copolymer using the metallocene compound of claim 13 .
15. The metallocene compound of claim 1 , wherein the compound of Chemical Formula 2e is any one of the following structural formulae:
16. A method of preparing an ethylene copolymer using the metallocene compound of claim 15 .Cited by (0)
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