Reacción #992710
ord-40737224341b4cf78d7a4122166ebaa4
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Otroequipped with a reflux condenser
- 2Temperaturacooled to room temperature
- 3Otroa solution obtained
- 4workup.ADDITIONwas gradually added dropwise over a period of 30 minutes
- 5workup.ADDITIONAfter completion of the dropwise addition
- 6Temperaturathe temperature was raised to 110° C.
- 7Temperaturathe mixture was refluxed for 5 hours
- 8FiltraciónThe deposited powder was filtered
- 9Lavadowashed with cold methanol
- 10Secadowith cold diethyl ether, and then dried
- 11Otroto obtain 0.79 g of a gold-phenanthroline complex (
Procedimiento
0.5 g of 1,10-phenanthroline (made by Wako Pure Chemical Industries, Ltd.) and 80 ml of distilled water were put in a 300-ml glass-made reaction vessel equipped with a reflux condenser, and the mixture was heated at 60° C. to dissolve the phenanthroline and cooled to room temperature. While the solution was stirred, a solution obtained by dissolving 1 g of tetrachloroauric acid (III) tetrahydrate in 17.2 ml of distilled water was gradually added dropwise over a period of 30 minutes. After completion of the dropwise addition, the temperature was raised to 110° C., the mixture was refluxed for 5 hours, and, then, 150 g of ammonium chloride was added to the resulting reaction solution to deposit orange powder. The deposited powder was filtered, washed with cold methanol and then with cold diethyl ether, and then dried to obtain 0.79 g of a gold-phenanthroline complex (hereinafter abbreviated as [Au(phen)Cl2]+Cl—).