Reaktion #80957

ord-7462102bc6c743e9b4de7098568f19de

Reaktionsgleichung

[Cl-].[Cl-].[Cl-].[Cl-].[Zr+4]
zirconium tetrachloride
C=CCCC(C)(C1C=CC=C1)C1c2ccccc2-c2ccccc21
5-cyclopentadienyl-5-(9-fluorenyl)-1-hexene
[Zr+2].c1cc[cH-]c1.c1cc[cH-]c1
zirconocene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was then evaporated in a vacuum
  2. 2
    SonstigeA white solid was recovered which
  3. 3
    Sonstigedried

Vorschrift

Then 1.61 g of the bridged ligand having a vinyl terminated branch, i.e. 5-cyclopentadienyl-5-(9-fluorenyl)-1-hexene, was dissolved in 10 mL of chlorodimethylsilane at room temperature. Then approximately 1 mL of hexachloroplatinic acid was added and a reaction mixture stirred overnight at room temperature. The solvent was then evaporated in a vacuum. A white solid was recovered which was concluded to be 1-chlorodimethyl-silyl-5-cyclopentadienyl-5-(9-fluorenyl)-hexane. A portion of this material was then contacted with silica gel (Merck No. 7734) the process involved contacting 2 g of the silica gel dried as explained in Example IV and 1.56 g of the 1-chlorodimethyl-silyl-5-cyclopentadienyl-5-(9-fluorenyl)-hexane in a manner analogous to that used in the analogous step in Example IV. Then a supported zirconocene was prepared by reacting 1.74 g of that solid with 0.8 g of zirconium tetrachloride using a technique of the general type disclosed in Example IV. The resulting supported metallocene will be referred to herein as catalyst 34A.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05616752uspto-grants-1997_04