Hostname: page-component-7479d7b7d-pfhbr Total loading time: 0 Render date: 2024-07-11T18:11:54.786Z Has data issue: false hasContentIssue false

On the Suitability of Lanthanides as Actinide Analogs

Published online by Cambridge University Press:  01 February 2011

Kenneth Raymond
Affiliation:
raymond@socrates.berkeley.edu, University of California, Chemistry, 531 Latimer Hall, Berkeley, CA, 94720-1460, United States
Geza Szigethy
Affiliation:
szigethy@berkeley.edu, University of California, Chemistry Department, Berkeley, CA, 94720-1460, United States
Get access

Abstract

With the current level of actinide materials used in civilian power generation and the need for safe and efficient methods for the chemical separation of these species from their daughter products and for long-term storage requirements, a detailed understanding of actinide chemistry is of great importance. Due to the unique bonding properties of the f-elements, the lanthanides are commonly used as structural and chemical models for the actinides, but differences in the bonding between these 4f and 5f elements has become a question of immediate applicability to separations technology. This brief overview of actinide coordination chemistry in the Raymond group at UC Berkeley/LBNL examines the validity of using lanthanide analogs as structural models for the actinides, with particular attention paid to single crystal X-ray diffraction structures. Although lanthanides are commonly accepted as reasonable analogs for the actinides, these comparisons suggest the careful study of actinide materials independent of their lanthanide analogs to be of utmost importance to present and future efforts in nuclear industries.

Type
Research Article
Copyright
Copyright © Materials Research Society 2008

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 Finch, Warren I., Geological, U.S. Survey Bulletin 2179-A (2003).Google Scholar
2 Bodvarsson, G. S., Boyle, W. Patterson, R. et al. , Journal of Contaminant Hydrology 38, 3 (1999).Google Scholar
3 Paiva, A. P. and Malik, P. J. Rad. Nuc. Chem. 261 (2), 485 (2004).Google Scholar
4 Gorden, A. E. V. Xu, J. and Raymond, K.N. Chem. Rev. 103, 4207 (2003).10.1021/cr990114xGoogle Scholar
5 Greenwood, N.N. and Earnshaw, A. Chemistry of the Elements. (Pergamon Press, New York, 1997).Google Scholar
6 Schreckenback, G. Hay, P. J., and Martin, R. L., J. Comp. Chem. 20, 70 (1999).Google Scholar
7 Gaunt, A. J., Reilly, S. D., Enriquiez, A. E. et al. , Inorg. Chem. 47, 29 (2008); M., Roger L. Belkhiri, T. Arliguie et al., Organometallics 27, 33 (2008).Google Scholar
8 Kepert, D.L. Inorganic Stereochemistry. (Springer-Verlag, New York, 1982).Google Scholar
9 Gorden, A. E. V. Shuh, D. K., Tiedemann, B. E. F. et al. , Chem. Eur. J. 11, 2842 (2005), 13, 378 (2007); A. E. V., Gorden, J., Xu G. Szigethy et al., J. Am. Chem. Soc. 129 (21), 6674 (2007); G., Szigethy, J., Xu, A. E. V., Gorden, et al., Eur. J. Inorg. Chem. Published online 28 Mar (2008).10.1002/chem.200401193Google Scholar
10 Xu, J. Radkov, E. Ziegler, M. et al. , Inorg. Chem. 39, 4156 (2000).Google Scholar
11 Looker, J. H., Prokop, R. J., Serbousek, W. E. et al. , J. Org. Chem. 44 (19), 3408 (1979).10.1021/jo01333a031Google Scholar
12 Hay, B. P., Uddin, J. and Firman, T. K., Polyhedron 23, 145 (2004).Google Scholar