2008
DOI: 10.1016/j.jlumin.2007.11.046
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Effect of ligands in two-photon excited luminescence of organometallic iridium complexes

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Cited by 7 publications
(7 citation statements)
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“…The output intensity of the two‐photon‐excited fluorescence was linearly dependent on the square of the input laser power (Figure S22 in the Supporting Information), thereby confirming nonlinear TPA. The TPA cross section of our probes is moderate compared with those of other iridium(III) complexes measured with a two‐photon laser‐induced phosphorescence method reported in the literature …”
Section: Resultsmentioning
confidence: 67%
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“…The output intensity of the two‐photon‐excited fluorescence was linearly dependent on the square of the input laser power (Figure S22 in the Supporting Information), thereby confirming nonlinear TPA. The TPA cross section of our probes is moderate compared with those of other iridium(III) complexes measured with a two‐photon laser‐induced phosphorescence method reported in the literature …”
Section: Resultsmentioning
confidence: 67%
“…complexes measured with at wo-photon laser-inducedp hosphorescence methodr eported in the literature. [37][38][39][40][41][42][43][44]…”
Section: Two-photon Absorption (Tpa) Cross Sectionsmentioning
confidence: 99%
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“…1 By contrast, far fewer metalbased chromophores have been investigated even though they possess attractive chemical and photophysical properties. [12][13][14][15][16] Second and third row transition metal oligopyridyl complexes lend themselves particularly well to non-linear processes. 17, 18 For instance, the rich photochemistry of the charge transfer excited triplet states of Ir (and Ru) complexes with an N 6 coordination sphere gives rise to long phosphorescent lifetimes in aerated fluid solution in the microsecond time domain.…”
Section: Introductionmentioning
confidence: 99%