関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Fluoranthene | HCID 9154 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | 3,8-Dibromofluoranthene | HCID 80783 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 3,8-Bis(biphen-4-yl)fluoranthene | HCID 57562109 | 14% |
反応手順
1 g of 3,8-dibromofluoranthene, prepared by dibromination of fluoranthene in chloroform with elemental bromine, was dissolved under protective gas in 100 ml of dried toluene and degassed repeatedly. 19.4 g of potassium carbonate dissolved in 47 ml of ethanol/water (1:1 parts by volume) and 1 g of 4-biphenylboronic acid were added and degassed again. Subsequently, 0.32 g of tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)4) was added under protective gas and the mixture was stirred at 80° C. for 16 hours. The reaction mixture was filtered and dried. Yield: 14% as a yellowish solid. λmax,em (toluene)=479 nm, quantum yield (toluene): 74%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07488856B2 |
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| 出典データセット | uspto-grants-2009_02 |
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| ORD ID | ord-d0c8c191593c4ec19f462db2062298cd |
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| 出典メモ | uspto-grants-2009_02 |
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