Reaktionsgleichung
[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2.[Cl-].[Hf+4:13].[Cl-].[Cl-].[Cl-].[OH2:17].N1CCCCC1.[CH2:24]([OH:26])C>>[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:24]([O-:26])=[O:17])[CH:8]=[CH:7]2.[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:24]([O-:26])=[O:17])[CH:8]=[CH:7]2.[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:24]([O-:26])=[O:17])[CH:8]=[CH:7]2.[OH:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:24]([O-:26])=[O:17])[CH:8]=[CH:7]2.[Hf+4:13]Komponenten
6
Versuchsvorschrift
To a solution of 8-Hydroxyquinoline (5.44 g, 37.5 mmol) in ethanol (200 mL, 95%) was added hafnium (IV) chloride (3.0 g, 9.37 mmol) in ethanol (100 mL), followed by a further 300 mL water. The pH of the solution was increased by dropwise addition of piperidine until a yellow precipitate forms. The resulting yellow precipitate was collected and washed with ethanol (100 mL, 95%), water (200 mL) and finally ethanol (100 mL, 95%). The sample was dried under vacuum at 80° C. until no further weight loss was detected. Sublimation (400° C., 10−6 Torr) yielded an analytical sample (4.5 g, 64%), m.p. 398° C.
Aufarbeitung
- customThe resulting yellow precipitate was collected
- washwashed with ethanol (100 mL, 95%), water (200 mL) and finally ethanol (100 mL, 95%)
- customThe sample was dried under vacuum at 80° C. until no further weight loss
- customSublimation (400° C., 10−6 Torr) yielded an analytical sample (4.5 g, 64%), m.p. 398° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-644951c6206f42fa8b2a98e7ef1e0ec4
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09437828B2
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