Abstract

The luminescence dynamics of a polypyridyl ruthenium II [Ru(phen)2(ip)]2+ and 5,10,15,20-tetraphenylporphyrin (H2TPP) dyad have been measured by using time-resolved fluorescence spectroscopy. The transient luminescent spectra of the dyad show an ultrafast energy transfer within 300 ps after photoexcitation of the [Ru(phen)2(ip)]2+ at 453 nm. However, no energy transfer has been observed as the excitation wavelength is 400 nm, corresponding to the absorption peak of H2TPP. The origin of the energy transfer from [Ru(phen)2(ip)]2+ to H2TPP has been analyzed according to the Forster energy-transfer theory.

© 2009 Chinese Optics Letters

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