Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylene | HCID 8252 | — |
| Reactant | 1-Hexene | HCID 11597 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 22386386 | HCID 22386386 | — |
Reaction Steps
A reaction vessel equipped with a mechanical stirrer, reflux condenser, and temperature control was dried and filled with nitrogen. The vessel was charged with 400 g of 1-hexene (from Ethyl Corp.), the temperature was adjusted to 25° C., and hydrogen (Oxygen Services ultra high purity) bubbled in at a rate of about 60 mL/min. 2.2 nL of a 1.8M solution of diethylaluminum chloride (from Aldrich Chemical Co.) was added followed by the addition of 0.4 g AATiCl3 and immediately propylene was bubbled into the reaction mixture at about 60 mL/min for 30 minutes. Methanol (20 mL) was added to terminate the polymerization and the polymer precipitated in excess methanol to extract the catalyst residues. A tacky amorphous polymer was obtained in 72% conversion having an inherent viscosity of 5.7 dL/g in n-hexane and a Tg of -32° C. 3C NMR analysis indicated that the polymer contained 87 mole percent of 1-hexene and 13 mole percent of propylene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859088 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-fefb83c532d34ebf8baa8b98eee21627 |
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| Source note | uspto-grants-1999_01 |
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