Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
27582 | Journal of Photochemistry and Photobiology A: Chemistry | 2011 | 6 Pages |
A new bis-quinolylimine ligand containing an azadiene moiety, 1,4-bis(2-quinolyl)-2,3-diaza-1,3-buthadiene (1), was synthesized by one-step facile condensation. This simple ligand, when dissolved in acetonitrile, shows a Cu2+-selective fluorescence enhancement. Coordination of 1 with Cu2+ produces two kinds of complexes with 1:1 and 1:2 stoichiometries. The 1:2 complex shows a strong fluorescence (ΦF = 0.37), while the 1:1 complex does not (ΦF < 0.01). Ab initio molecular orbital calculation reveals that the 1:1 complex has a distorted structure, while the 1:2 complex has a planar structure. The planar configuration of the 1:2 complex, therefore, allows an extended π-conjugation over the entire molecule and, hence, results in fluorescence enhancement.
Graphical abstractA bis-quinolylimine ligand, 1, shows a Cu2+-selective fluorescence enhancement by a formation of 1–Cu2+ 1:2 complex with a planar configuration, leading to an extended π-conjugation over the entire molecule.Figure optionsDownload full-size imageDownload as PowerPoint slide