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Acta Cryst. (2005). E61, o2001-o2002 [ doi:10.1107/S1600536805016442 ]
Abstract: In the complex between p-cumylcalix[4]arene and para-xylene [systematic name: 4-(2-phenylisopropyl)calix[4]arene-1,4-dimethylbenzene (1/1)], C64H64O4·C8H10, the macrocycle has a cone conformation, which is stabilized by intramolecular hydrogen bonds. The guest para-xylene molecule is situated inside the cavity, giving an endo-calix complex. The host and guest molecules both have twofold rotation symmetry.
Online 10 June 2005
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