Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | Bicyclo(2.2.1)hept-5-en-2-ol | HCID 96066 | — |
| Catalyst | Bis(1,5-cyclooctadiene)nickel | HCID 6433264 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethylene 5-norbornen-2-ol | HCID 86594155 | 829% |
Reaction Steps
A glass reactor was loaded inside a glove box with L(iPr2)Ni(ηl-CH2Ph)(PMe3) (about 20 μmol; 2.00 g of 8.77 mM solution in toluene), Ni(COD)2 (about 50 μmol; 2.50 g of 17.6 mM solution in toluene), 5-norbornen-2-ol (about 1.99 mmol; 3.00 g of 0.578 M solution in toluene) and toluene (about 18.45 g) such that the total volume of the toluene solution was about 30 mL. The glass reactor was sealed inside the glove box and was attached to a vacuum/nitrogen line manifold. Ethylene was fed continuously into the reactor at about 100 psi and the pressurized reaction mixture was stirred at about 20° C. Ethylene was vented after about 20 minutes and acetone was added to quench the polymerization. The precipitated polymer was collected by filtration and dried under high vacuum overnight. The reaction produced about 1.14 g of ethylene/5-norbornen-2-ol co-polymer. The activity of the catalyst with respect to ethylene consumption was about 156 kg mol−1 h−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259214B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-39c8df0c99a043cfb2ad4d4034f3e3d9 |
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| Source note | uspto-grants-2007_08 |
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