Reaction of solids of pure D 2 d and D 2 C 84, as well as mixtures of these isomers, with an excess of potassium produces the cubic phases K 8+ x C 84, with multiple occupancy of the octahedral site by potassium. Analysis of X-ray powder diffraction data reveals that the anions adopt well-defined orientations in the solid, driven by the anion−cation contacts. Electron paramagnetic resonance measurements on the solid fullerides indicate that the electronic properties depend on the particular isomer of C 84 used as host.
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Allen et al. (1998) studied this question.
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