Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2'-Bipyridine | HCID 1474 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Butyl Acrylate | HCID 8846 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21546549 | HCID 21546549 | — |
Reaction Steps
To 0.11 g (6.68×10−4 mole) 2,2′-bipyridine and 0.036 g (2.34×10−4 mole) CuBr at −30° C. in a glass tube, was added 1.75 mL (2×10−2 mole) isobutene, 0.5 mL (0.55×10−2 mole) butyl acrylate (BA) and 0.040 mL (2.34×10−4 mole) diethyl methyl bromomalonate under an argon atmosphere. The glass tube was sealed under vacuum and the reaction mixture warmed to 50° C. for 12 hours. The reaction mixture was then dissolved in THF and the conversion of BA as determined by GC was 100%. The polymer was then precipitated into methanol (three times), filtered, dried at 60° C. under vacuum for 48 h and weighted. Mn=3180, Mw/Mn=1.38 (Mth=3400). The content of isobutene in the copolymer was determined by integration of C(O)OCH2 from butyl acrylate and the gem-dimethyl region of the 1H-NMR spectrum was 49%. The Tg of product, as determined by DSC, was −48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06541580B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-6b28539b44a14cd4a9c4c0fc245c1c3b |
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| Source note | uspto-grants-2003_04 |
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