Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | 1-Dodecanethiol | HCID 8195 | — |
| Reactant | Butyl Acrylate | HCID 8846 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21092714 | HCID 21092714 | 75.5% |
Reaction Steps
Into a 1 l four-necked flask, 8.0 g of acrylic acid, 13.5 g of n-butyl acrylate, 28.5 g of methyl methacrylate, 10.0 g of 2,2'-azobisisobutylonitrile (AIBN), 5.0 g of n-dodecylmercaptan and 500 ml of dioxane were charged, dissolved and stirred. Then, stirring was continued under a nitrogen stream at 70° C. for 6 hours. The reaction solution was put into n-hexane to precipitate the resin. Purification with tetrahydrofuran/n-hexane was repeated, followed by vacuum drying at 40° C. to obtain a resin powder. The obtained amount was 43.0 g. The weight average molecular weight as measured by GPC was 15,000 as calculated as polystyrene; the glass transition temperature (Tg) was 53° C.; and the acid value calculated after titration by means of a potentiometer was 60. 25 g of a methacrylic acid/n-butyl acrylate/methyl methacrylate copolymer thus obtained, 4.5 g of a melamine-type heat-curing agent (hexamethoxymethylolmelamine, CYMEL (trademark) 303, manufactured by Mitsui Cyanamid) and 75 g of diethylene glycol dimethyl ether were mixed and dissolved, followed by filtration with a 0.2 μm filter to obtain a planarizing material solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677380 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-ed5158bd86d94fba8fbe483e9e63e21d |
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| Source note | uspto-grants-1997_10 |
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