Abstract

Thermolysis of the diruthenium compound [(η6-cymene)RuCl2]2 (1) with ClRe(CO)5 (2) leads to the formation of the new confacial bioctahedral compound (η6-cymene)Ru(μ-Cl)3Re(CO)3 (3) in good yields; the same product has also been isolated when a mixture of 1 and 2 is irradiated with near UV–vis light for an extended period of time. Heating 1 and ClMn(CO)5 (4) does not furnish the corresponding manganese analogue of 3 but rather the trioctahedral halide-bridged product [fac-ClRu(CO)3]2(μ-Cl)4Mn(H2O)2 (5). 3 and 5 have been fully characterized in solution and their molecular structures established by X-ray crystallography. Thermolysis of [(η6-cymene)RuCl2]2 (1) with the respective pentacarbonyl ClM(CO)5 [where M = Re (2); Mn(4)] affords the halide-bridged compounds (η6-cymene)Ru(μ-Cl)3Re(CO)3 (3) and [fac-ClRu(CO)3]2(μ-Cl)4Mn(H2O)2 (5). 3 and 5 have been isolated and characterized spectroscopically in solution and their molecular structures established by X-ray crystallography.

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