Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Catechol | HCID 289 | — |
| Edukt | Oxygen | HCID 977 | — |
| Edukt | 1,12-Dodecanediamine | HCID 17727 | — |
| Lösungsmittel | Trichloroethylene | HCID 6575 | — |
| Lösungsmittel | 1,2,3-Trichloropropane | HCID 7285 | — |
| Produkt | HCID 131719865 | HCID 131719865 | — |
Reaktionsschritte
About 14.54 g (0.0782 mol) 2-phenyl-hydrooquinone, about 0.2 g (0.0018 mol) catechol (chemical name 1,2-dihydroxybenzene) and about 16 g (0.08 mol) 1,12diaminododecane were dissolved in a solvent mixture comprising of about 30 mL of 1,2,3trichloropropane and 60 mL of trichloroethylene. Oxygen was then passed at a flow rate of about 50 cc/min through the solution for about one hour. About 0.2 g of cupric sulfate was then added to the reaction mixture. Oxygen flow was reinstated for about an additional two hours. At the end of the polymerization reaction most of the trichloroethylene was removed under high vacuum, without raising the temperature above 35° C. This solution of poly-(2-phenyl-benzoquinone-1,12-diaminododecane) polymer can be used directly for coating purposes.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05606010 |
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| Quelldatensatz | uspto-grants-1997_02 |
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| ORD ID | ord-abe3001167674f86ba1595956f75f223 |
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| Quellennotiz | uspto-grants-1997_02 |
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