Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Azobisisobutyronitrile | HCID 6547 | — |
| Edukt | tert-Butyl acrylate | HCID 15458 | — |
| Edukt | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Edukt | 3-Hydroxy-1-methacryloyloxyadamantane | HCID 11856523 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Hydroxystyrene | HCID 138202 | — |
Reaktionsschritte
To a round bottom flask equipped with condenser, thermometer, an argon (Ar) inlet, and a magnetic stirrer bar, the following were added: 4-acetoxystyrene monomer (2.43 grams (g), 0.015 mole), t-butyl acrylate monomer (1.6 g, 0.0125 mole), 3-hydroxy-1-adamantyl methacrylate monomer (5.319 g, 0.0225 mole), 2,2′-azobis(2-methylpropionitrile) (AIBN)(0.328 g, 4% of total moles of monomers), and approximately 40 g of tetrahydrofuran (THF). The reaction mixture was stirred at room temperature and bubbled with Ar flow for 45 minutes before it was heated. The reaction was carried out overnight at 72° C. under an inert Ar atmosphere. The rest of the synthetic procedures are the same as Example 1, except approximately 5 g of concentrated NH4OH was used in deprotecting the acetoxy groups from acetoxystyrene repeat units to form hydroxyl styrene repeat units of the terpolymer.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08557501B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-faa677eb57fb4c8691417a68a05654cf |
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| Quellennotiz | uspto-grants-2013_10 |
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