Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | tert-Butyl methacrylate | HCID 11448 | — |
| Reactant | 3-(Trimethoxysilyl)propyl methacrylate | HCID 17318 | — |
| Reactant | Methyl bicyclo[2.2.1]hept-5-ene-2-carboxylate | HCID 250075 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131726005 | HCID 131726005 | — |
Reaction Steps
To 25 ml of tetrahydrofuran in 100 ml of a round-shaped flask were added 5 g of 3-(trimethoxysilyl)propyl methacrylate, 4 g of t-butyl methacrylate, 3 g of methyl 5-norbornene-2-carboxylate and 1 g of methacrylic acid. Then, 0.13 g of AIBN (azobisisobutyronitrile) as a polymerization initiator was added to the resulting mixture, and reacted at 67° C. under a nitrogen atmosphere for 24 hours. Next, the resulting mixture was cooled at room temperature, and poured into a beaker including 500 ml of ethyl ether to precipitate the resulting mixture. Thereafter, the precipitate was filtered and dehydrated at room temperature, thereby obtaining poly(3-(trimethyoxysilyl)propyl methacrylate/t-butyl methacrylate/methyl 5-norbornene-2-carboxylate/methacrylic acid) having a molecular weight of 1,900 represented by Formula 1a (yield: 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129023B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-2e285d7c2c734e08b2f501b7b0d4f07d |
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| Source note | uspto-grants-2006_10 |
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