Hostname: page-component-848d4c4894-4rdrl Total loading time: 0 Render date: 2024-06-25T20:15:16.865Z Has data issue: false hasContentIssue false

Trivalent Europium Complexes Using Dendritic â-Diketone Ligands

Published online by Cambridge University Press:  15 February 2011

Patrick J. Case
Affiliation:
Loker Hydrocarbon Research Institute, Department of Chemistry, University of Southern California, Los Angeles, CA 90089-1661.
Aaron W. Harper
Affiliation:
Loker Hydrocarbon Research Institute, Department of Chemistry, University of Southern California, Los Angeles, CA 90089-1661.
Get access

Abstract

A series of photon harvesting lanthanide complexes have been synthesized by chelating dendritic â-diketone ligands to Eu+3. The ligands are modified benzoyltrifluoroacetone units (BTFA) with poly(aryl ether) dendron attachments. These ligands impose a very large asymmetric nature to the first coordination sphere of europium compared to previous dendritic compounds. These complexes exhibit europium emission with no residual emission from the ligands as the dendritic subunits increase from G-0 to G-3. This is due to both antenna and site isolation effects. These complexes mimic light harvesting organisms seen in Nature. When these intensities are compared throughout the series, an increase in intensity is seen where [(G2)BTFA]3Eu is the brightest, with [(G3)BTFA]3Eu being less intense than the G-2 complex. However, the lifetime data indicates that the G-3 complex is the longest lived species.

Type
Research Article
Copyright
Copyright © Materials Research Society 2003

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Parker, D. and Williams, J. A., J. Chem. Soc., Dalton Trans. 18, 36133628 (1996).Google Scholar
2. Kuriki, K., Koike, Y., and Okamoto, Y., Chem. Rev. 102, 23472356 (2002).Google Scholar
3. Kido, J. and Okamoto, Y., Chem. Rev. 102, 23572368 (2002).Google Scholar
4. Sabbatini, N., Guardigli, M., and Lehn, J. M., Coordin Chem. Rev. 123, 201228 (1993).Google Scholar
5. Fréchet, J. M. J., Science 263, 1710 (1994).Google Scholar
6. Hawker, C. J. and Fréchet, J. M. J., J. Am. Chem. Soc. 112, 7638 (1991).Google Scholar
7. Okada, K., Wang, Y., Chen, T., Kitamura, M., Nakaya, T., and Inoue, H., J. Mater. Chem. 9, 30233026 (1999).Google Scholar
8. Uekawa, M., Ikeda, Y. Miyamoto, Kaifu, K., and Nakaya, T., Synthetic Metals 91, 259262 (1997).Google Scholar
9. Melby, L. R., Rose, N. J., Abramson, F., and Caris, J. C., J. Am. Chem. Soc. 86, 5117 (1964).Google Scholar
10. Ferreira, L. F. V., Costa, S. N. B., and Perereira, E. J., J. Photochem. Photobiol. A. 55, 361376 (1991).Google Scholar
11. Kawa, M. and Fréchet, J.M. J., Chem. Mater. 10, 286 (1998).Google Scholar
12. Wooley, K. L., Klug, C. A., Tasaki, K., and Schaefer, J., J. Am. Chem. Soc. 119, 5358 (1997).Google Scholar