EP0485823B1
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EP
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2-Substituted bisindenyl-metallocenes, process for their preparation and their use as catalysts for the polymerization of olefins
Assignee: Novolen Technology Holdings CV
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Filing: 1991-11-01
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Granted: 1995-03-08
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Expires: 2011-11-01
Abstract
No abstract record available.
Inventors
- 👤 Andreas Dr. Winter
- 👤 Martin Dr. Antberg
- 👤 Walter Dr. Spaleck
- 👤 Jürgen Dr. Rohrmann
- 👤 Volker Dr. Dolle
Bibliographic Details
Application Number
—
Jurisdiction
EP
Data Source
google_patents
Last Synchronized
2026-10-29 09:56
CPC Classifications
C; C08; C08F; C08F110/00; C08F110/04; C08F110/06; C07; C07F; C07F17/00; C07F7/00; C07F7/02; C07F7/08; C07F7/0803; C07F7/0805; C08F10/00; C08F4/00; C08F4/42; C08F4/44; C08F4/60; C08F4/62; C08F4/639; C08F4/63912; C08F4/6392; C08F4/63922; C08F4/63927; Y; Y10; Y10S; Y10S526/00; Y10S526/943
Claims Analysis
Total Claims: 4
Claim 1
Independent Claim
350 words
A process for the preparation of a compound of the formula I in which M¹ is a metal from group IVb, Vb or VIb of the Periodic Table, R¹ and R² are identical or different and are a hydrogen atom, a C₁-C₁₀-alkyl group, a C₁-C₁₀-alkoxy group, a C₆-C₁₀-aryl group, a C₆-C₁₀-aryloxy group, a C₂-C₁₀-alkenyl group, a C₇-C₄₀-arylalkyl group, a C₇-C₄₀-alkylaryl group, a C₈-C₄₀-aryl-alkenyl group or a halogen atom, R³ and R⁴ are identical or different and are a hydrogen atom, a halogen atom, a C₁-C₁₀-alkyl group, which may be halogenated, a C₆-C₁₀-aryl group, an -NR₂¹⁰, -SR¹⁰, -OSiR₃¹⁰, SiR₃¹⁰ or -PR₂¹⁰ radical in which R¹⁰ is a halogen atom, a C₁-C₁₀-alkyl group or a C₆-C₁₀-aryl group, R⁵ and R⁶ are identical or different and are as defined for R³ and R⁴, with the proviso that R⁵ and R⁶ are not hydrogen, R⁷ is =BR¹¹, =AlR¹¹, -Ge-, -Sn-, -O-, -S-, =SO, =SO₂, =NR¹¹, =CO, =PR¹¹ or =P(O)R¹¹, where R¹¹, R¹² and R¹³ are identical or different and are a hydrogen atom, a halogen atom, a C₁-C₁₀-alkyl group, C₁-C₁₀-fluoroalkyl group, a C₆-C₁₀-aryl group, a C₆-C₁₀-fluoroaryl group, a C₁-C₁₀-alkoxy group, a C₂-C₁₀-alkenyl group, a C₇-C₄₀-arylalkyl group, a C₈-C₄₀-arylalkenyl group or a C₇-C₄₀-alkylaryl group, or R¹¹ and R¹² or R¹¹ and R¹³, in each case with the atoms connecting them, form a ring, M² is silicon, germanium or tin, R⁸ and R⁹ are identical or different and are as defined for R¹¹, and m and n are identical or different and are zero, 1 or 2, m plus n being zero, 1 or 2, which comprises reacting a compound of the formula II where R³-R⁹, m and n are as described in the formula I, and M³ is an alkali metal, preferably lithium, a) with a compound of the formula III M¹X₄ (III) in which M¹ is as defined in the formula I, and X is a halogen atom, preferably chlorine, or b) with a compound of the formula IIIa M¹X₄L₂ (IIIa) in which M¹ and X are as defined above, and L is a donor ligand, and, if desired, derivatizing the resultant reaction product.
Claim 2
Dependent Claim
59 words
The process as claimed in claim 1, wherein, in the formula I, M¹ is Zr or Hf, R¹ and R² are identical or different and are methyl or chlorine, R³ and R⁴ are hydrogen, R⁵ and R⁶ are identical or different and are methyl, ethyl or trifluoromethyl, R⁷ is a radical, and n plus m is zero or 1.
Claim 3
Dependent Claim
37 words
The process as claimed in claim 1 or 2, wherein the compound of the formula I is rac-dimethylsilyl(2-methyl-1-indenyl)₂zirconium dichloride, rac-ethylene(2-methyl-1-indenyl)₂zirconium dichloride, rac-dimethylsilyl(2-methyl-1-indenyl)₂dimethylzirconium, rac-ethylene(2-methyl-1-indenyl)₂dimethylzirconium, rac-phenyl(methyl)silyl(2-methyl-1-indenyl)₂zirconium dichloride, rac-diphenylsilyl(2-methyl-1-indenyl)₂zirconium dichloride, rac-methylethylene(2-methyl-1-indenyl)₂zirconium dichloride, rac-dimethylsilyl(2-ethyl-1-indenyl)₂zirconium dichloride, rac-ethylene(2-ethyl-1-indenyl)₂zirconium dichloride, rac-isopropylidene(2-methyl-1-indenyl)₂zirconium dichloride or rac-phenyl(methyl)silyl(2-methyl-1-indenyl)₂methylzirconium.
Claim 4
Dependent Claim
28 words
The use of a compound of the formula I as claimed in one or more of claims 1 to 3 as a catalyst in the polymerization of olefins.
References Cited (Backward Citations)
No citation records indexed.
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