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  • A new combination to form a solid solution: a solid solution consisting of a stabilized phenoxyl radical and its methoxy analogue.
  • https://doi.org/10.1107/s2053229625011441Copy DOI Icon

A new combination to form a solid solution: a solid solution consisting of a stabilized phenoxyl radical and its methoxy analogue.

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Abstract

A new combination of molecules that form a solid solution is reported. The 2,4,6-tris(4-tert-butylphenyl)phenoxyl radical, C36H41O (1M), formed two solid solutions (α and β) with its methoxy analogue 1,3,5-tris(4-tert-butylphenyl)-2-methoxybenzene, C37H44O (1OMe). According to single-crystal X-ray analysis, the crystal structure of each solid solution is thought to be dominated by the characters of the main components. The β crystal (1M:1OMe = 0.002:0.998) is isomorphic to the crystal composed solely of 1OMe and the molecules in the β crystal adopt the most preferred conformation for 1OMe. In contrast, in the α crystal (1M:1OMe = 0.80:0.20), the molecules adopt the most preferred conformation for 1M. However, since a crystal composed solely of 1M has not been obtained (1M always precipitates as a σ-dimer formed by a covalent C-O bond between the phenoxyl O atom of one molecule and the para-C atom of the central phenyl ring of another molecule), it is unclear whether it is isomorphic with the α crystal.

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