Studies of Ruthenium Complexes. IV. The Solvent Effect on the Isotopic Ligand-exchange Reaction of the cis- Dibromotetraammineruthenium(III) Complex

• Published in: Bulletin of the Chemical Society of Japan Vol. 46; no. 7; pp. 2133 - 2136
• Main Authors: Ohyoshi, Akira, Shinohara, Tetsuo, Hosoyamada, Yoshihiro, Yamada, Takato, Hiroshima, Yutaka
• Format: Journal Article
• Language: English
• Published: Tokyo The Chemical Society of Japan 01.07.1973; Chemical Society of Japan
• ISSN: 0009-2673; 1348-0634
• DOI: 10.1246/bcsj.46.2133

The isotopic ligand-exchange reactions of cis-dibromotetraammineruthenium(III) were studied in aqueous and methanol-water solutions in order to distinguish them from those in the case of the monobromocomplex and in order to ascertain the role of the water molecule with respect to the reaction mechanism. In an aqueous solution, the reaction proceeds through the rate-determining aquation step with the SN2 mechanism: Ru(NH3)4Br2++H2O→Ru(NH3)4(H2O)Br2++Br−, Ru(NH3)4(H2O)Br2++*Br−→Ru(NH3)4Br*Br++H2O. This result is similar to that for the monobromocomplex. In the methanol solution (H2O∼1.5%), the exchange reaction proceeds through the SN1 mechanism: Ru(NH3)4Br2+→Ru(NH3)4Br2++Br−, Ru(NH3)4Br2++*Br−→Ru(NH3)4Br*Br+. When the concentration of water becomes very low, the number of solvated water molecules decreases; therefore, the coordinated bromide ion may easily be liberated. When the concentration of water is higher than 10%, the rate constant increases with the increase in the water concentration. Since the electronic spectra did not change during the exchange reaction, it would seem that the water molecule attacks a cis-position as a nucleophile. These results can be interpreted by postulating a hydrogen-bond between the proton of the water molecule and the coordinated bromide ion.