Solvent control of the photolabilization pathways from the ligand field excitation of [Rh(NH3)5Cl]2+
Abstract
It is demonstrated that the identity of the ligand labilized from the ligand field excited states of [Rh(NH3)5Cl]2+ is a function of the solvent medium, with Cl– substitution predominating in water and formamide solutions but NH3 substitution predominating in dimethylformamide, methanol, and dimethyl sulphoxide solutions.
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