Abstract
According to our solution reactivity studies, the reactant [H(dmso)2]2[IrCl6] undergoes slow spontaneous reduction of Ir(IV) to Ir(III) in all solvents under study, including water, hydrochloric acid, and acetone. A concurrent reaction is realized in acetone solutions, which effectively gives rise to the incorporation of DMSO into the iridium coordination sphere to afford trans-[IrIIICl4(dmso)2]â. The chemical evolution of [H(dmso)2]2[IrCl6] extends beyond the iridium-centered complex anion.
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