Abstract
Slow co-crystallization of a solution of benzene-1,3,5-tricarboxylic acid with a large excess of 4-hydroxypyridine produces an interpenetrating, three-dimensional, hydrogen-bonded framework consisting of three 4-pyridone and one benzene-1,3,5-tricarboxylic acid molecules, C9H6O6·3C5H5NO. This structure represents an orthorhombic polymorph of the previously reported C-centered, monoclinic structure [Campos-Gaxiola et al. (2014). Acta Cryst. E70, o453-o454].
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Staun, S. L., & Oliver, A. G. (2015). Crystal structure of benzene-1,3,5-tricarboxylic acid-4-pyridone (1/3). Acta Crystallographica Section E: Crystallographic Communications, 71, 1283–1286. https://doi.org/10.1107/S2056989015017867
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