Hits:
Indexed by:期刊论文
Date of Publication:2012-08-21
Journal:JOURNAL OF MATERIALS CHEMISTRY
Included Journals:SCIE、EI、Scopus
Volume:22
Issue:31
Page Number:15757-15768
ISSN No.:0959-9428
Abstract:Fluorene-containing N boolean AND N Pt(II) bisacetylide complexes were prepared, in which the fluorene moieties were connected to the Pt(II) center via acetylide bonds (-C C-). Different aryl groups were attached to the fluorene moiety, such as phenylacetylide (Pt-4), naphthalimide-4-acetylide (Pt-1) and in Pt-2, the fluorene moiety was changed to carbozale moiety. We found that with the fluorene linker between the arylacetylide and the Pt(II) center, the absorption of complexes in the visible range were intensified. All the complexes show room temperature (RT) phosphorescence. Furthermore, Pt-1 shows much longer triplet excited state lifetime (tau = 138.1 mu s) than the analogue Pt-3 (tau = 47.4 mu s). For Pt-2, with changing the fluorene moiety to carbazole moiety, the T-1 state lifetime becomes much shorter (tau = 23.0 mu s). Thus the one-atom (N vs. C) difference is crucial for the photophysical properties. The triplet excited state of Pt-1 was proved to be the intraligand excited state ((IL)-I-3) by nanosecond time-resolved transient absorption spectroscopy, spin density analysis and emission at 77 K. The complexes were used as triplet sensitizers for triplet-triplet annihilation (TTA) upconversion. Upconversion quantum yield (Phi(UC)) up to 24.3% was observed for Pt-1. Under the same conditions the model complex Pt-4 shows no upconversion. The overall upconversion efficiency (eta) of the new complexes are improved compared to the model complexes, such as Pt-2, Pt-3 and Pt-4. The improved upconversion efficiency was attributed to either the prolonged T-1 excited state lifetime or the intensified absorption in the visible range. Our study on the fluorene-containing N boolean AND N Pt(II) bisacetylide complexes will be useful for designing new phosphorescent Pt(II) complexes and for their applications.
Pre One:Visible light-harvesting cyclometalated Ir(III) complexes as triplet photosensitizers for triplet-triplet annihilation based upconversion
Next One:Excited state intramolecular proton transfer (ESIPT): from principal photophysics to the development of new chromophores and applications in fluorescent molecular probes and luminescent materials