Multiple charge-transfer emissions from different metal-ligand pairs in ruthenium diimines.

Ruthenium diimines are unique in their emissivity. Optical excitation with light of less than 500 nm leads to a strong emission in the 600-700 nm range. All emissive ruthenium complexes appear to undergo intersystem crossing from the absorptive singlet metal-to-ligand charge-transfer (MLCT) state to an emissive triplet MLCT state localized on the lowest-energy metal-ligand pair.

Optical memory and multistep luminescence thermochromism in single crystals of K2Na[Ag(CN)2]3.

Single crystals of the layered compound K2Na[Ag(CN)2]3 exhibit a dual emission with high-energy (HE) and low-energy (LE) phosphorescence bands at 313 and 402 nm, respectively. Remarkably, the crystals exhibit "optical memory", in which a new emission band with intermediate energy (IE) at 380 nm is generated upon laser irradiation (lambda ex = 266 nm) at cryogenic temperatures. The irradiated crystals reinstate their original luminescence spectrum upon heating to room temperature and then recooling.

Tunable photoluminescence of closed-shell heterobimetallic Au-Ag dicyanide layered systems.

The excited-state properties of the layered La[Ag(CN)(2)](3) and La[Au(CN)(2)](3) systems have been examined and compared with mixed-metal systems of varying metal ratios such as La[Ag(0.78)Au(0.22)(CN)(2)](3), La[Ag(0.

Metallophilic interactions in closed-shell d10 metal-metal dicyanide bonded luminescent systems Eu[Ag(x)Au(1-x)(CN)2]3 and their tunability for excited state energy transfer.

We report on the heterobimetallic system, Eu[Ag(x)Au(1-x)(CN)(2)](3) (x = 0-1) in which sensitization of europium luminescence occurs by energy transfer from [Ag(x)Au(1-x)(CN)(2)](-) donor excited states. The donor states have energies which are tunable and dependent on the Ag/Au stoichiometric ratio. These layered systems exhibit interesting properties, one of which is their emission energy tunability when excited at different excitation wavelengths.

Structural studies of lanthanide ion complexes of pure gold, pure silver and mixed metal (gold-silver) dicyanides.

Crystal structures of four lanthanide complexes of La[Au(CN)2](3).3H2O, La[Ag(CN)2](3).3H2O, La[Ag(0.