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Two basic heterocyclic imino structures display a planar backbone with similar features, but differ in the heterocyclic atoms located in the five-membered rings, i.e. N and S. In the pyrrole, centrosymmetric imino­pyrrole dimers are assembled by means of two inverted N—H...N hydrogen bonds and two inverted C—H...π inter­actions. In the thio­phene, however, mol­ecules are linked by nonclassical C—H...N hydrogen bonds in which the mol­ecules play the roles of both hydrogen-bond donors and acceptors, resulting in one-dimensional supra­molecular chains.
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