Fluorene- and carl;azole-bridged dipyridyl ligands potentially useful for t
he construction of supramolecules by self-assembly processes have been synt
hesized by palladium-catalyzed cross-coupling reactions. They undergo facil
e ring closure reactions with Re(CO)(5)X (X = Cl, Br) to form molecular geo
metries of varied dimensions. Fluorene-bridged ditopic ligands facilitate t
he formation of trimetallic triangles, while the angular carbazole-bridged
ligands led to the formation of cyclic dimers. The ligands are strongly emi
tting in the blue region, and the:supramolecules display emission of differ
ent origins triggered by the bridging aromatic segment. Carbazole-containin
g cyclic dimers emit green light that probably originates from a ligand-loc
alized excited state. However, in the fluorene-based triangles emission was
observed only at low temperature, and it displayed (3)pi-pi* and (MLCT)-M-
3-based emissions with prolonged lifetimes.