Abstract
The crystal structures of [N(CH3)4]2HgCl4 between 191 K and 350 K have been studied by single crystal X-ray diffraction. Below Tc1 = 277 K the structure is monoclinic P21/a with lattice parameters a = 12.320 (7), b = 9.034 (4), c = 15.402 (4) Å, and β = 89.64 (1)° at T = 191 K. Above Tc1 the structure is orthorhombic Pnma with lattice parameters 12.419 (7), b = 9.068 (4), and c = 15.684 (2) Å at room temperature, and with lattice parameters a = 12.421 (9), b = 9.125 (1), and c = 15.777(4) Å at T = 350 K. At room temperature each TMA cation disorderly occupies two orientations (TMA is tetramethylammonium). At low temperature the structure is fully ordered, with additional shifts and rotations of all ions, in accordance with the results of Asahi et al., J. Phys. Soc. Jpn. 60 (1991) 921. Refinements using restrictions of the non-crystallographic tetrahedral point group for the TMA cations and refinements without restrictions are used to show that TMA has tetrahedral symmetry at all temperatures. The HgCl4 anions are distorted, but the distortions are independent of the temperature. The phase transition at Tc1 is described as an order/disorder transition accompanied by major rotations and shifts of the ions. New evidence for a previously reported phase transition at Tc2 = 320 K (Zangar et al. Phase Transitions 12 (1988) 141) is obtained from NMR. This transition is shown to be a non symmetry breaking structural transition, that correspond to a gradual loss of the orientational order of the TMA cations.
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