Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9776480 | Synthetic Metals | 2005 | 4 Pages |
Abstract
We report the structures and physical properties of new βâ²-(BEDT-TTF)4[Fe(oxalate)3]·G salts where A = H3O+, G = PhCl; A = Rb+ G = Pyridine. The structure of the PhCl salt is isomorphous with βâ²-(BEDT-TTF)4[(H3O)M(oxalate)3] with other guest molecules. PhCl is ordered in die hexagonal pockets formed by the [(H3O)Fe(oxalate)3] layer. The electrical conductivity is metallic down to 100 K, below which the resistivity increases with decreasing temperature. The specific conductivity at room temperature is about 10 S/cm. We also report the salt βâ²-(BEDT-TTF)4[RbFe(oxalate)3]·Pyridine where Rb+ replaces H3O. The electrical resistivity shows metallic behavior down to 100 K. and turns up gradually to a maximum at 65 K below which the system re-enters the metallic state down to liquid helium temperature. Neither salt shows superconductivity down to 2 K. In addition, other new βâ²-(BEDT-TTF)4[(H3O)M(oxalate)3]·salts with M = Cr, Ga, Fe; G = CH2Cl2, CH2ClBr, CH2Br2 are also reported.
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Authors
A. Akutsu-Sato, A. Kobayashi, T. Mori, H. Akutsu, J. Yamada, S. Nakatsuji, S.S. Turner, P. Day, D.A. Tocher, M.E. Light, M.B. Hurstho,