HCID 178461830, compound → HCID 178461830, compound
Reaction equation
[Cl-:1].[Cl-].[CH:3]([Zr+2:6]([CH:12]1[C:24]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[C:18]2[C:13]1=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:7]1[CH:11]=[CH:10][CH:9]=[CH:8]1)([CH3:5])[CH3:4]>C1(C)C=CC=CC=1>[Zr:6].[Cl-:1].[Cl-:1].[CH:3]([Zr+2:6]([CH:12]1[C:24]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[C:18]2[C:13]1=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:7]1[CH:11]=[CH:10][CH:9]=[CH:8]1)([CH3:5])[CH3:4]Participants
4
Reactant 1
Product 2
Reagents, catalysts & solvents 1
Procedure
The preparation of the supported catalyst is repeated analogously to Example 1 with the difference that 65 mg (0.15 mmol) of isopropyl (9-fluorenyl)cyclopentadienyl-zirconium dichloride are dissolved in 40 ml of toluene and added dropwise to the suspension of 3.9 g of "MAO on SiO2, type B" in 60 ml of toluene. Analysis of the pale-red filtrate gives a zirconium content of 0.9 mg (corresponding to 4.3 mg of isopropyl-(9-fluorenyl)cyclopentadienylzirconium dichloride). 3 g of free-flowing, violet, supported catalyst containing 20 mg of zirconocene per gram of catalyst are obtained.
Workup
- customThe preparation of the supported catalyst
Sources & evidence
- ORD record
- ord-81e666e92aa24b8aa7b0f4b9f6427319
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05719095
Reaction notes
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