Abstract

The lifetimes of Cr(NH 3) 6 3+ and the Cr(cyclam)(NH 3) 2 + complexes, both protiated and deuterated, have been recorded in aqueous polyalcoholic and DMSO solutions in the temperature range that includes the change from a rigid glass to a fluid. A small but distinct lifetime reduction is associated with increased solvent mobility in the protiated species but not in the deuterated complex. This is interpreted to indicate that increasing anharmonicity in accepting modes enhances the nonradiative rates.

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