Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Stilbene | HCID 11502 | — |
| Edukt | Benzene, 1,3-bis(1-phenylethenyl)- | HCID 118622 | — |
| Edukt | 1,4-Bis(1-phenylethenyl)benzene | HCID 5242314 | — |
| Produkt | 1,1-Diphenylethylene | HCID 10740 | — |
Reaktionsschritte
For instance, in accordance with an embodiment of the present inveniton, a living macrocarbocation, e.g., living cationic polyisobutylene, is reacted with a double diphenylethylene, e.g., 1,3-bis(1-phenylethenyl)benzene (sometimes referred to as meta-double diphenylethylene) or 1,4-bis(1-phenylethenyl)benzene (sometimes referred to as para-double diphenylethylene), to produce a 1,1-diphenylethylene end-functionalized carbocationic polymer. The carbocation is then alkylated with a suitable alkylating agent, e.g., with an organometallic compound such as dimethylzinc, whereupon the resulting macromonomer is readily metallated with a suitable organometallic compound such as an alkyllithium compound, thereby providing a living anionic macroinitiator in near quantitative yield. A sterically hindered lithium compound, e.g., a 1,1-diphenylalkyllithium species, is used in certain embodiments to remove impurities that may be present alongside the 1,1-diphenylethylene end-functionalized polymer, thereby preventing premature termination of the living macroanion.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07056985B2 |
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| Quelldatensatz | uspto-grants-2006_06 |
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| ORD ID | ord-9fbca44ee16f4ba08f982fb4ed559920 |
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| Quellennotiz | uspto-grants-2006_06 |
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