Self-assembly molecular architectures incorporating fluorene- and carbazole-based bichromic oligopyridines. Novel photoactive materials

Citation
Krj. Thomas et al., Self-assembly molecular architectures incorporating fluorene- and carbazole-based bichromic oligopyridines. Novel photoactive materials, ORGANOMETAL, 20(11), 2001, pp. 2262-2269
Citations number
47
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANOMETALLICS
ISSN journal
02767333 → ACNP
Volume
20
Issue
11
Year of publication
2001
Pages
2262 - 2269
Database
ISI
SICI code
0276-7333(20010528)20:11<2262:SMAIFA>2.0.ZU;2-5
Abstract
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.