Heterobimetallic complexes [Cu(N.ident.C-Cy-C.ident.N)2][Au(C6F5)2]·0.5 Toluene (1) and [Cu(N.ident.C-Cy-C.ident.N)2][Au(C6F5)2]·CH2Cl2 (2) and [AuCu(C6F5)2(N.ident.C-Cy-C.ident.N)2]·CH2Cl2 (3) (with the same stoichiometry but different structure) have been synthesized and the crystal structure of complex 2·CH2Cl2 has been characterized through X-ray diffraction studies. The structure shows a cationic [Cu(N.ident.C-Cy-C.ident.N)2]+ polymer that runs parallel to the crystallog. y axis, which is formed by the copper centers and the nitrile bridging ligands, and [Au(C6F5)2]- anions that link the polymeric chain via non-classical C-H···Au hydrogen bonds. Complexes 1, 2 and 3 only differ in the solvents and the time used for their synthesis but this greatly affects their photophys. properties. Complexes 1, 2 and 3 are brightly luminescent in solid state at room temp. with lifetimes in the microseconds range. Complexes 1 and 2 display emissions arising from IL transitions while for complex 3 an emission arising from a MLCT is proposed. [on SciFinder(R)]
CITATION STYLE
Fernandez, E. J., Laguna, A., Lopez-de-Luzuriaga, J. M., Monge, M., Montiel, M., Olmos, M. E., & Rodriguez-Castillo, M. (2008). Solvent Induced Luminescence in Supramolecular Heterobimetallic Gold(I)-Copper(I) Complexes with a Bidentate Nitrile Ligand. The Open Inorganic Chemistry Journal, 2(1), 73–79. https://doi.org/10.2174/1874098700802010073
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