Abstract
An expression is derived from first principles that indicates a 10<sup>4</sup> improvement in the detection limit for trace metal analyses by use of crystalline energy transfer instead of normal luminescence methods. These calculations were experimentally verified by examining a crystal comprised of tris-(2,2'-bipyridine) zinc (II) dichloride [Zn(bipyr)<sub>3</sub>Cl<sub>2</sub>] as the host and tris-(2,2'-bipyridine) ruthenium (II) dichloride [Ru(bipyr)<sub>3</sub>Cl<sub>2</sub>] as the emitting guest. With this system subnanogram levels of ruthenium could be measured. To verify the possibility of crystalline energy transfer quenching analysis a three component crystal was examined that had a fixed concentration of the ruthenium chelate and a varying amount of tris-(2,2'-bipyridine) iron (II) dichloride [Fe(bipyr)<sub>3</sub>Cl<sub>2</sub>] as the quenching agent. With this system nanogram levels of iron could be measured.
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