反応式
[Tb:1].[C:2]1([P:8](=[O:21])([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(O)C>[C:2]1([P:8](=[O:21])([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1.[Tb:1]参加物
4
実験手順
Terbium tris 2,2,6,6-tetramethylheptanedionate (1 g) and triphenylphosphine oxide (0.393 g) were added to anhydrous ethanol (3 ml). The mixture was warmed to dissolve the solid, and then raised to boiling for 10 minutes. The solution was cooled to room temperature and then to 0° C. to induce crystallisation of the product. The off-white solid was filtered off and recrystallised from anhydrous ethanol and dried in vacuo at 60° C. to yield tris 2,2,6,6-tetramethylheptanedionato terbium triphenylphosphine oxide adduct (0.9 g) as a white solid.
後処理
- temperatureThe mixture was warmed
- dissolutionto dissolve the solid
- temperatureraised
- customto 0° C.
- customcrystallisation of the product
- filtrationThe off-white solid was filtered off
- customrecrystallised from anhydrous ethanol
- customdried in vacuo at 60° C.
出典と根拠
- ORDレコード
- ord-b63e696d05774b3695b5d3a49898f859
- 出典データセット
- uspto-grants-2007_09
- 特許番号
- US07270770B2
関連ノート
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