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论文类型：期刊论文

发表时间：2011-06-14

发表刊物：DALTON TRANSACTIONS

收录刊物：PubMed、SCIE、EI

卷号：40

期号：22

页面范围：5953-5963

ISSN号：1477-9226

摘要：We studied four cyclometallated Pt(II) complexes, in which the thiazo-coumarin ligands (Pt-2, Pt-3 and Pt-4) or the phenylthiazo ligand (Pt-1) were directly cycloplatinated. Pt-2 shows intense absorption in visible region but other complexes show blue-shifted absorption. Room temperature phosphorescence was observed for all the complexes, and the emission wavelength is dependent on the size of the pi-conjugation, not the intramolecular charge transfer (ICT) feature of the (CN)-N-boolean AND ligands. Pt-2 shows longer phosphorescence lifetime (tau = 20.3 mu s) than other complexes (below 2.0 mu s). Furthermore, Pt-2 shows phosphorescence quantum yield Phi = 0.37, whereas Pt-3 and Pt-4 show much smaller Phi values (0.03 and 0.01, respectively). DFT/TDDFT calculations indicate (IL)-I-3 triplet excited states for the complexes. The complexes were used as for luminescence O-2 sensing and triplet-triplet-annihilation (TTA) based upconversion. Stern-Volmer quenching constant K-SV = 0.026 Torr(-1) was observed for Pt-2, ca. 89-fold of that of Pt-3. TTA upconversion is achieved with Pt-2 (lambda(em) = 400 nm with lambda(ex) = 473 nm, anti-Stokes shift is 0.47 eV, excitation power density is at 70 mW cm(-2)). The upconversion quantum yield with Pt-2 as triplet sensitizer is up to 15.4%. The TTET efficiency (K-SV = 1.33 x 10(5) M-1, k(q) = 6.57 x 10(9) M-1 s(-1). DPA as quencher) of Pt-2 is 34-fold of the model complex [Ru(dmb)(3)][PF6](2). Our results show that the (IL)-I-3 state can be readily accessed by direct cyclometallation of organic fluorophores and this approach will be useful for preparation and applications of transition metal complexes that show intense absorption in visible region and the long-lived emissive (IL)-I-3 excited states.