Toluene → 2-Butylcyclopenta-1,3-diene;zirconium(4+);dichloride

HRID 1952392Notes

Reaction equation

HRID 1952392 reaction equation
C1(C)C=CC=CC=1.[Cl-:8].[Cl-].[CH2:10]([C:14]1([Zr+2:19]C2(CCCC)C=CC=C2)[CH:18]=[CH:17][CH:16]=[CH:15]1)[CH2:11][CH2:12][CH3:13].C=C>CO>[CH3:13][CH2:12][CH2:11][CH2:10][C:14]1[CH:15]=[CH:16][CH2:17][C-:18]=1.[CH3:13][CH2:12][CH2:11][CH2:10][C:14]1[CH:15]=[CH:16][CH2:17][C-:18]=1.[Cl-:8].[Cl-:8].[Zr+4:19]

Participants

5

Conditions

Temperature
40 °C

Procedure

To a 500 mL four-necked flask equipped with magnetic stirrer was charged 250 mL of toluene. The toluene was heated to 34° C. To this was added a toluene solution of 0.038 g (1.4 mmol) of polymethylaluminoxane composition based on aluminum atoms. Bis(n-butylcyclopentadienyl)zirconium dichloride ((nBu-Cp)2ZrCl2) was added to achieve an Al/Zr mole ratio of 5,000. While raising the temperature to 40° C., ethylene gas was blown in. After 10 minutes, the ethylene gas feed was halted and methanol was introduced to deactivate the catalyst. The polyethylene produced was filtered and dried. The polymerization activity was calculated to be 140×106 g-PE/mol-Zr·atm·hr. The polymer obtained was in the form of smooth microparticles that did not adhere to the reaction apparatus following polymerization.

Workup

  1. customTo a 500 mL four-necked flask equipped with magnetic stirrer

Sources & evidence

ORD record
ord-107d1674453d4a089b7ee3f31398fd1e
Source dataset
uspto-grants-2013_03
Patent number
US08404880B2

Reaction notes

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