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Long‐Lived Luminescent Dendrimers with a [Ru(dpp) 3 ] 2+ ‐Type Core: Synthesis and Photophysical Properties
Author(s) -
Hahn Uwe,
Vögtle Fritz,
De Paoli Gabriele,
Staffilani Mara,
De Cola Luisa
Publication year - 2009
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200900253
Subject(s) - chemistry , ruthenium , luminescence , dendrimer , acetonitrile , photochemistry , excited state , phenanthroline , conjugated system , crystallography , polymer chemistry , catalysis , organic chemistry , physics , optoelectronics , polymer , nuclear physics
Metallodendrimers built around a [Ru(dpp) 3 ] 2+ ‐type core (dpp = 4,7‐diphenyl‐1,10‐phenanthroline) were prepared containing peripheral phenyl moieties. The convergent synthesis of the ligands was accomplished by coupling dendritic branches with a focal amino function to the chelating phenanthroline precursor under the formation of sulfonamide linkages. Complexation of ruthenium ions afforded the corresponding metallodendrimers with up to 24 peripheral phenyl units in the case of the largest dendritic structure. The absorption spectra and luminescence properties of the four new dendrimers are reported. The dendritic effect is clearly visible, going from zero to second generation, as demonstrated by an elongation in the excited‐state lifetime in aerated acetonitrile and improved emission quantum yields relative to the reference complex containing a [Ru(dpp) 3 ] 2+ core. Interestingly, the use of rigid and conjugated ruthenium‐based cores results, for all dendritic structures, in luminescence lifetimes that are several microseconds long in deaerated solutions, even at room temperature.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)