Abstract
Five X-ray structures of complexes of ethyl resorcinarene with aromatic nitrogen heterocycles (imidazole, 1,2,4-triazole, pyridine, pyrazine, 2-pyridylmethanol and quinoline) show that ethyl resorcinarene spontaneously forms molecular inclusion complexes with five- and six-membered aromatic nitrogen heterocycles via π ⃛π and CH ⃛π interactions. However, with 10-membered quinoline, no molecular inclusion complex is formed. Instead, quinoline manifests crystal lattice inclusion.
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