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US5591879A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for preparing cyclopentadienyl-type ligands

Assignee: Phillips Petroleum Co
•
Filing: 1995-06-23
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Granted: 1997-01-07
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Expires: 2015-06-23
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Abstract

Abstract In accordance with the present invention there is provided a cyclopentadienyl-type ligand represented by the formula ZA, wherein Z is a cyclopentadienyl-type group, wherein A is --YPR 2 , --YNR 2 , or --NR 2 , wherein Y is an alkylene group containing 1 to 24 carbon atoms, wherein each R is individually selected from alkyl groups containing 1 to 20 carbon atoms. Another aspect of the invention is to provide a metallocene represented by the formula ZAMX 3 , wherein Z and A are as described above, M is a Group IVB or VB transition metal, and X is a halide. Other aspects of the present invention include catalyst systems comprising the metallocenes and an organoaluminoxane, processes for preparing the above defined ligands, metallocenes and catalyst systems, and polymerization processes employing the catalyst systems.

Inventors

  • 👤 Krisztina Frey
  • 👤 Gabriele von Massow
  • 👤 Helmut G. Alt
  • 👤 M. Bruce Welch

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 01:49
CPC Classifications
C; C08; C08F; C08F10/00; C07; C07F; C07F17/00; C07F9/00; C07F9/02; C07F9/28; C07F9/50; C07F9/5018; C08F110/00; C08F110/02; C08F210/00; C08F210/16; C08F4/00; C08F4/42; C08F4/44; C08F4/60; C08F4/62; C08F4/639; C08F4/63912; C08F4/63916; C08F4/6392; C08F4/64; C08F4/659; C08F4/65912; C08F4/6592; Y; Y10; Y10S; Y10S526/00; Y10S526/943

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 234 words
A process for preparing a cyclopentadienyl-type ligand comprising: (1) reacting a halosilane with an alkali metal salt of a cyclopentadienyl-type compound to form a silylcyclopentadienyl-type compound, wherein said halosilane compound containing a cyclopentadienyl-type group is represented by the formula X"Si(R 1 ) 3 , wherein X" is a halide and wherein each R 1 is individually an alkyl group containing 1 to 20 carbon atoms or hydrogen, wherein said cyclopentadienyl-type group is an unsubstituted cyclopentadienyl, substituted cyclopentadienyl, unsubstituted indenyl, substituted indenyl, unsubstituted fluorenyl, or substituted fluorenyl group, wherein the substituents on said cyclopentadienyl-type group are hydrocarbyl groups containing 1 to 12 carbon atoms, alkoxy groups containing 1 to 12 carbon atoms, trialkylsilyl groups where each alkyl group contains 1 to 12 carbon atoms, alkyl halide groups where the alkyl group contains 1 to 12 carbon atoms, or halide; (2) reacting said silylcyclopentadienyl-type compound with an alkali metal alkyl containing 1 to 8 carbon atoms and methylene chloride, to produce a chloromethylated silylcyclopentadienyl-type compound; and then (3) reacting said chloromethylated silylcyclopentadienyl-type compound with a nucleophile to produce said cyclopentadienyl-type ligand, wherein said nucleophile is represented by the formula JA, wherein J is an alkali metal, wherein A is --YPR 2 , --YNR 2 , or --NR 2 , wherein Y is an alkylene group containing 1 to 24 carbon atoms, wherein each R is individually selected from alkyl groups containing 1 to 20 carbon atoms.
Claim 2
Dependent Claim 234 words
A process for preparing a cyclopentadienyl-type ligand comprising: (1) reacting a halosilane with an alkali metal salt of a cyclopentadienyl-type compound to form a silylcyclopentadienyl-type compound, wherein said halosilane compound containing a cyclopentadienyl-type group is represented by the formula X"Si(R 1 ) 3 , wherein X" is a halide and wherein each R 1 is individually an alkyl group containing 1 to 20 carbon atoms or hydrogen, wherein said cyclopentadienyl-type group is an unsubstituted cyclopentadienyl, substituted cyclopentadienyl, unsubstituted indenyl, substituted indenyl, unsubstituted fluorenyl, or substituted fluorenyl group, wherein the substituents on said cyclopentadienyl-type group are hydrocarbyl groups containing 1 to 12 carbon atoms, alkoxy groups containing 1 to 12 carbon atoms, trialkylsilyl groups where each alkyl group contains 1 to 12 carbon atoms, alkyl halide groups where the alkyl group contains 1 to 12 carbon atoms, or halide; (2) reacting said silylcyclopentadienyl-type compound with an alkali metal alkyl containing 1 to 8 carbon atoms and methylene chloride, to produce a chloromethylated silylcyclopentadienyl-type compound; and then (3) reacting said chloromethylated silylcyclopentadienyl-type compound with a nucleophile to produce said cyclopentadienyl-type ligand, wherein said nucleophile is represented by the formula JA, wherein J is an alkali metal, wherein A is --YPR 2 , --YNR 2 , or --NR 2 , wherein Y is an alkylene group containing 1 to 24 carbon atoms, wherein each R is individually selected from alkyl groups containing 1 to 20 carbon atoms.
Claim 3
Dependent Claim 16 words
A process according to claim 1 wherein said halosilane is chlorotrimethylsilane and wherein J is lithium.
Claim 4
Dependent Claim 18 words
A process according to claim 1 wherein said cyclopentadienyl-type group is an unsubstituted fluorenyl or substituted fluorenyl group.
Claim 5
Dependent Claim 24 words
A process according to claim 3 wherein Y contains 1 to 20 carbon atoms and wherein each R contains 1 to 10 carbon atoms.
Claim 6
Dependent Claim 24 words
A process according to claim 4 wherein Y contains 1 to 16 carbon atoms and wherein each R contains 1 to 5 carbon atoms.
Claim 7
Dependent Claim 23 words
A process according to claim 5 wherein Y is an unsubstituted or substituted methylene or ethylene group and wherein each R is methyl.
Claim 8
Dependent Claim 22 words
A process according to claim 6 wherein the substituents on said cyclopentadienyl-type group are alkyl groups containing 1 to 10 carbon atoms.
Claim 9
Dependent Claim 18 words
A process according to claim 7 wherein the substituents are alkyl groups containing 1 to 6 carbon atoms.
Claim 10
Dependent Claim 16 words
A process according to claim 8 wherein A is --CH 2 P(CH 3 ) 2 .

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