Reaktion #992710

ord-40737224341b4cf78d7a4122166ebaa4

Reaktionsgleichung

[Cl-].[NH4+]
ammonium chloride
c1cnc2c(c1)ccc1cccnc12
phenanthroline
[Cl][Au-]([Cl])([Cl])[Cl].[H+]
tetrachloroauric acid
c1cnc2c(c1)ccc1cccnc12
1,10-phenanthroline
[Au].c1cnc2c(c1)ccc1cccnc12
Gold Phenanthroline

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeequipped with a reflux condenser
  2. 2
    Temperaturcooled to room temperature
  3. 3
    Sonstigea solution obtained
  4. 4
    workup.ADDITIONwas gradually added dropwise over a period of 30 minutes
  5. 5
    workup.ADDITIONAfter completion of the dropwise addition
  6. 6
    Temperaturthe temperature was raised to 110° C.
  7. 7
    Temperaturthe mixture was refluxed for 5 hours
  8. 8
    FiltrationThe deposited powder was filtered
  9. 9
    Waschenwashed with cold methanol
  10. 10
    Trocknenwith cold diethyl ether, and then dried
  11. 11
    Sonstigeto obtain 0.79 g of a gold-phenanthroline complex (

Vorschrift

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—).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08012628B2uspto-grants-2011_09