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The packing density of various structures is important not only for understanding and the prediction of high-pressure phase transitions, but also because of its reported correlation with thermodynamic stability. Plotting the cube root of formula volume against the cation radii (R) for nine morphotropic series with isolated tetrahedral anions, A2MO4 (M = Si, Ge, S, Se, Cr, Mn, Mo, W) and A2BeF4, permits the comparison of packing densities for 13 structure types (about 80 individual compounds and several solid solutions) stable at (or near) ambient temperature. The spinel type is the densest. The next densest types are those of K2MoO4, Tl2CrO4, β-Ca2SiO4, β-K2SO4, Ag2CrO4 and Sr2GeO4. In three series (M = Ge, Mo, W) the densest type comes with somewhat intermediate values of R, and not the largest, in contrast to the classical homology rule. Another contradiction with traditional views is that some of the densest phases have abnormally low overall binding energies. The correlation between packing density and coordination number (CN) is better when CN of A counts entire MX4 groups rather than individual X atoms; many, but not all, A2MX4 structures have binary A2M analogues (of course, A and M are not necessarily the same in these structure types). The most frequent arrangement of A around M is of the Ni2In type: a (distorted) pentacapped trigonal prism.

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