Tuning the emission properties of cyclometalated platinum(II) complexes by intramolecular electron-sink/arylethynylated ligands and its application for enhanced luminescent oxygen sensing

We have synthesized five novel cyclometalated Pt(II) complexes (aryl-ppy)Pt(acac) (ppy = 2-phenyl pyridine, aryl = N-butyl naphthalimide (NI) ethynylene for Pt-1, N-butyl naphthalimide (NI)-CH sub(2)-CO-for Pt-2,4-cyanophenyl-CH sub(2)-CO-for Pt-3, naphthal ethynylene for Pt-4 and naphthal-diketo fo...

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Veröffentlicht in:Journal of materials chemistry 2010-11, Vol.20 (43), p.9775-9786
Hauptverfasser: Wu, W, Ji, S, Guo, H, Song, P, Han, K, Chi, L, Shao, J, Zhao, J
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Sprache:eng
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Zusammenfassung:We have synthesized five novel cyclometalated Pt(II) complexes (aryl-ppy)Pt(acac) (ppy = 2-phenyl pyridine, aryl = N-butyl naphthalimide (NI) ethynylene for Pt-1, N-butyl naphthalimide (NI)-CH sub(2)-CO-for Pt-2,4-cyanophenyl-CH sub(2)-CO-for Pt-3, naphthal ethynylene for Pt-4 and naphthal-diketo for Pt-5). For the first time, pi -conjugation of the ppy ligands was extended via the CsC bond. Deep red/near IR emission (638 nm-700 nm) was observed for the complex containing naphthalimide ethynylene subunit (Pt-1), whereas the close analogue Pt-2 (in which the linker between the NI and the ppy subunit is a -CH sub(2)CO- group) shows a relatively blue-shifted emission (540 nm-570 nm) but much longer luminescent lifetime ( tau = 25.5 mu s) than Pt-1 ( tau = 6.6 mu s). Simultaneous fluorescence/phosphorescence emissions were observed for Pt-1 and Pt-2, but other complexes show sole phosphorescent emission. The red-shifted phosphorescence of the complexes compared to the model complex ppyPt(acac) (486 nm) was attributed to either the significant electron-sink effect of the NI fragment (Pt-1) (for which the electron withdrawing effect is stronger than the previously reported fluoren-9-one), or the extended pi -conjugation of the ppy ligand (via C=C bond) (e.g. Pt-4). The substantial tuning of the emission color and the luminescent lifetimes (0.86 mu s-25.5 mu s) of the complexes were rationalized by theoretical calculations (DFT/TDDFT), i.e. the emissive triplet excited states were assigned as the normal super(3)MLCT state (give smaller tau values) or the novel ligand-localized super(3)IL emissive state (give larger tau values). With tuning the luminescent lifetimes, the luminescent O sub(2) sensitivity of the complexes was improved by 117-fold (Stern-Volmer quenching constants K sub(sv) = 0.234 Torr super(-1) for Pt-2 vs. K sub(sv) = 0.002 Torr super(-1) for Pt-5).
ISSN:0959-9428
1364-5501
DOI:10.1039/c0jm01794a