Magnetically Driven Structural Phase Transition in Hexamethylbenzene

The methyl groups in hexamethylbenzene C6(CH3)6 become magnetically ordered at the molecular level below 118 K. This is also near the temperature at which the system structurally transitions from triclinic to a unique near-cubic phase. High-precision measurements of the near-static dielectric constant reveal that the structural phase transition actually comprises four successive transformations upon cooling at T 1 = 110.7 K, T 2 = 109.5 K, T 3 = 109.1 K, and T 4 = 107.8 K. In contrast to warming, only two transitions occur at T′4 = 119.2 K and T′1 = 120.9 K. The methyl groups in the near-cubic phase become slightly distorted according to existing neutron powder diffraction measurements. Analysis of the 26 = 64 possible spin orientation configurations of the methyl groups reveal a 20-fold ground state degeneracy presiding in each molecule rendering the system to become highly unstable. From such, it is interpreted that T 1 and T 2 are temperatures at which the molecules successively lower their symmetry to remove the energy degeneracy, which involve methyl group elongation and further out-of-plane tilting. This triggers the system to phase transition into the near-cubic phase, which involves a shearing of the molecular planes and partial rotation of the methyl groups at T 3 and T 4. We interpret the low temperature near-cubic phase to be a manifestation of Jahn–Teller distortions based on energy degeneracies of the orbital motion of protons in each molecule and suggest that the metastable nature of the phase transition originates from the methyl groups requiring a larger amount of energy to order than to disorder. Our findings help explain why many unusual structural phase transitions occur at low temperatures in other molecular crystals possessing periodic motion of protons.