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Interesting Electronic Properties Generated by Metal-Ion Linked C60 Chains

Published online by Cambridge University Press:  25 February 2011

D. J. Singh
Affiliation:
Department of Chemistry, Temple University, Philadelphia, PA
Y. C. Fann
Affiliation:
Department of Chemistry, Temple University, Philadelphia, PA
S. A. Jansen
Affiliation:
Department of Chemistry, Temple University, Philadelphia, PA
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Abstract

Recently it has been shown that buckminsterfullerene can be made to crystallize in a fee lattice when doped with various alkali metals eg. K, Rb, etc. Preliminary studies have shown the high propensity of C60 to be reduced without loss of stability. This may lead to interesting conductive pathways if a suitable dopant can be found which would act as an electronic “bridge” between adjacent “buckyballs” Out theoretical analyses have been geared towards a greater understanding of the reductive tendencies of C60, to discover how hypothetical metal-ion/C60, complexes differ from their corresponding simple, well characterized organometallic analogs. We demonstrate that the “metallocenium” link perturbs the electronic states of the C6 moiety including the frontier molecular Orbitals. Consequently, the metal ion plays an important role in establishing the electronic characteristics of metal-ion linked C60, chains and can be used to achieve desired properties.

Type
Research Article
Copyright
Copyright © Materials Research Society 1992

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References

REFERENCES

1. Stephens, P.W., Mihaly, L., Wiley, J.B., Huang, S-M., Kaner, R.B., Diederich, F., Whetten, R.L. and Holczer, K., submitted to Phvs. Rev. B Rapid Commun.Google Scholar
Kratschmer, W., Lamb, L.D., Fostiropoulos, R.D., Huffman, R.D., Nature 347, 354(1990).Google Scholar
2. see for example Krusic, P.J., Wasserman, E., Keizer, P.N., Morton, J.R. and Preston, K.F., Science, 254, 1183(1991).Google Scholar
Fowler, P.W., Lazzeretti, P. and Zanasi, R., Chem. Phvs. Lett, 165(1). 79(1990).Google Scholar
Ciolowski, J., J. Amer. Chem. Soc. 113, 4139(1991).Google Scholar
3. Iqbal, Z., Baughman, R.H., Ramakrishna, B.L., Khare, S., Sanjeeva Murthy, N., Bornemann, H.J. and Morris, D.E., Science. 254, 826(1991).Google Scholar
Kelly, S.P., Chen, C. and Lieber, M., Nature 352, 223(1991).Google Scholar
4. Stephens, P.W., Mihaly, L., Lee, P.L., Whetten, R.L., Huang, S-M., Kaner, R., Diederich, F. and Holczer, K., Nature. 351, 632(1991).Google Scholar
Hawkins, J.M., Meyer, A., Lewis, T.A., Loren, S. and Hollander, F.J., Science. 113, 3190(1991).Google Scholar
5. Hoffman, R., J. Chem Phvs, 39, 1397(1963).Google Scholar
Hoffman, R. and Lipscomb, W.M., J. Chem Phvs, 36, 3179(1962).Google Scholar
6. for a discussion of the η-2 and η-5 link, see Albright, T.A., Burdett, J.K. and Whangbo, M-H., Orbital Interactions in Chemistry; John Wiley & Sons: New York, 1985; Chapters 17 & 19.Google Scholar