Abstract
A series of d-f heterodimetallic bisporphyrin complexes (YbZn, YbPd, and YbPt), in which a YbIII porphyrinate moiety is linked to a transition-metal porphyrinate moiety by a flexible three-carbon chain, were synthesized. They were fully characterized by high-resolution mass spectrometry, 1H and 31P NMR spectroscopy, electronic absorption, and fluorescence methods. Variable-temperature near-infrared photoluminescence studies showed that the transition-metal porphyrinate moiety would enhance the ytterbium(III) emission centered at about 998 nm and extend its emission lifetime. YbPd and YbPt showed large two-photon absorption cross-section values because of the interaction between the porphyrin units, which caused a loss of centrosymmetry. Optical limiting investigation demonstrated that [Yb(TPP)(L OMe)] and YbPt have comparable performance to C60 by virtue of their heavy-metal effect. Our results indicate that these bisporphyrin dimetallic complexes will find valuable applications in the field of nonlinear optics.
Original language | English |
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Pages (from-to) | 3365-3374 |
Number of pages | 10 |
Journal | European Journal of Inorganic Chemistry |
Issue number | 21 |
DOIs | |
Publication status | Published - 2007 |
Scopus Subject Areas
- Inorganic Chemistry
User-Defined Keywords
- Lanthanides
- Optical limiting
- Photoluminescence
- Porphyrins
- Transition metals