Abstract
Co-intercalation of methylamine molecules into the cubic K3C60 lattice affords the fulleride (CH3NH2)K3C60, which was characterized by Raman and MAS 13C and 1H NMR spectroscopy. The high-resolution synchrotron X-ray powder diffraction technique was employed to determine its crystal structure at ambient temperature. We find that CH3NH2 bonds to K+ ions residing in the pseudo-octahedral interstices, thereby providing an efficient and facile route to hyperexpanded close-packed strongly anisotropic fulleride lattices, while retaining the electronic contact between the C603- anions. Preliminary evidence for the occurrence of a transition to an antiferromagnetic state at low temperature is also presented, consistent with the proximity of the present system to the metal-insulator boundary of the electronic phase diagram of C603- fullerides.
| Original language | English |
|---|---|
| Pages (from-to) | 14784-14785 |
| Number of pages | 2 |
| Journal | Journal of the American Chemical Society |
| Volume | 128 |
| Issue number | 46 |
| Early online date | 31 Oct 2006 |
| DOIs | |
| Publication status | Published - 1 Nov 2006 |
| Externally published | Yes |
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