Journal
RSC ADVANCES
Volume 2, Issue 3, Pages 1061-1067Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ra00434d
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Funding
- NSFC [20972024, 21073028]
- Fundamental Research Funds for the Central Universities [DUT10ZD212, DUT11LK19]
- Ministry of Education [SRFDP-200801410004, NCET-08-0077]
- Royal Society (UK)
- NSFC (China-UK Cost-Share Science Networks) [21011130154]
- Education Department of Liaoning Province [2009T015]
- Dalian University of Technology
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Difluoroboron (BF2) bound phenylacetylide was attached to the Pt(II) center of (NN)-N-boolean AND Pt(II) bisacetylide complex (Pt-1). Enhanced absorption in the visible region (epsilon = 1.37 x 10(4) M-1 cm(-1) at 434 nm) and emissive (IL)-I-3 excited state (tau = 0.92 mu s, Phi = 3.3%) were observed for Pt-1, compared to the model complex dbbpy Pt(II) bisphenylacetylide (Pt-2, tau = 0.90 ms, Phi = 40.0%. dbbpy = 4,4'-di-tertbutyl- 2,2'-bipyridine). Pt-1 was used as the triplet sensitizer for triplet-triplet annihilation (TTA) based upconversion and an upconversion quantum yield (Phi(UC)) of 8.9% was observed with 9,10-diphenylanthracence (DPA) as the triplet acceptor. In comparison, no upconversion was observed for the model complex Pt-2.
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