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Evaporation of mixed solution of 2,4,6-tris(4-tert-butylphenyl)phenoxyl 1M and its phenol analogue 1OH yielded a solid solution (III), where 1OH : 1M = 0.70 : 0.30, which was isomorphic to crystal of 1OH (II). In contrast, slow evaporation of 1M concomitant with gradual decomposition giving 1OH yielded crystal-glass composite (IV) consisting of 1OH : 1M with a molar ratio of 0.40 : 0.60. The outer crystal region of IV was attributed to solid solution of 1OH and 1M, while the inner glassy region to amorphous consisting of 1M and its dimer 1D (I).

Preparation of solid solution and crystal-glass composite consisting of stable phenoxyl radical and its phenol analogue