Visible light-harvesting cyclometalated Ir(III) complexes as triplet photosensitizers for triplet-triplet annihilation based upconversion

Visible light-harvesting cyclometalated Ir(III) complexes with 3-(2-benzothiazoly)-7-diethylaminocoumarin as the C^N cyclometalation ligands were prepared. The ancillary N^N ligand is either 6-piperidine naphthalimide-phenanthroline (Ir-1) or 9-aminophenanthroline (Ir-3). Ir(ppy)(2)(Phen) was prepar...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2012-09, Vol.41 (35), p.10680-10689
Hauptverfasser: Ma, Lihua, Guo, Huimin, Li, Qiuting, Guo, Song, Zhao, Jianzhang
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Sprache:eng
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Zusammenfassung:Visible light-harvesting cyclometalated Ir(III) complexes with 3-(2-benzothiazoly)-7-diethylaminocoumarin as the C^N cyclometalation ligands were prepared. The ancillary N^N ligand is either 6-piperidine naphthalimide-phenanthroline (Ir-1) or 9-aminophenanthroline (Ir-3). Ir(ppy)(2)(Phen) was prepared as model complex (Ir-2). Ir-1 and Ir-3 show strong absorption of visible light (ε = 109,000 M(-1) cm(-1) or 112,000 M(-1) cm(-1) at 486 or 484 nm, respectively). All the complexes show room temperature phosphorescence with drastically different phosphorescence quantum yields (Φ(P) = 4.3%, 44.3% and 46.0% for Ir-1, Ir-2 and Ir-3, respectively). With steady state and time-resolved spectra, as well as DFT calculations, the T(1) excited states of Ir-1 and Ir-3 were proposed to be the (3)IL state, whereas the (3)MLCT state was proposed for Ir-2. Long-lived emissive triplet excited states (7.6 μs and 54.5 μs) were observed for Ir-1 and Ir-3, compared to the short T(1) excited state lifetime of Ir-2 (1.2 μs). The complexes were used as triplet photosensitizers for triplet-triplet annihilation upconversion and upconversion quantum yields (Φ(UC)) of 19.3% and 12.7% were observed for Ir-1 and Ir-3, respectively. No upconversion was observed for Ir-2 under the same experimental conditions.
ISSN:1477-9226
1477-9234
DOI:10.1039/c2dt30955f