Reaction #992710
ord-40737224341b4cf78d7a4122166ebaa4
Reaction equation
Reagents
Conditions
Workup
- 1Otherequipped with a reflux condenser
- 2Temperaturecooled to room temperature
- 3Othera solution obtained
- 4workup.ADDITIONwas gradually added dropwise over a period of 30 minutes
- 5workup.ADDITIONAfter completion of the dropwise addition
- 6Temperaturethe temperature was raised to 110° C.
- 7Temperaturethe mixture was refluxed for 5 hours
- 8FiltrationThe deposited powder was filtered
- 9Washwashed with cold methanol
- 10Dryingwith cold diethyl ether, and then dried
- 11Otherto obtain 0.79 g of a gold-phenanthroline complex (
Procedure
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—).