Reports on crystal structures of calix[n]arenes, revealing diverse architectures and interactions, suggesting implications for molecular design.
This paper reports six crystal structures of five calix[ n ]arenes ( n = 4, 6, or 8), highlighting the remarkable ability of this molecular class to self-assemble into diverse architectures and conformations, and rationalizing which structural features predispose calixarenes to act as supramolecular hosts. The structures of p -sulfonatocalix[4]arene and 1,3-bis(carboxymethyl)calix[4]arene reveal open-crown conformations accessible to guest molecules, both in the calcium salt and DMSO solvate forms, respectively. Closed-crown conformations were identified in two conformational polymorphs of hexakis(carboxymethyl)calix[6]arene methyl ester and in a lower-rim n -butyl-functionalized p-tert -butylcalix[8]arene derivative, in which their first crystal structures are reported here. Meanwhile, the p-tert -butylcalix[8]arene without lower-rim functionalization crystallizes with two structurally similar pleated-loop conformers that display distinct packing motifs. Hirshfeld surface analyses and DFT help us also to understand the interactions patterns and conformerism, such as the finding of an atypical high-energy 1,2,3-alternate conformer in which the closed crown is kept by π···π interactions between phenyl rings in one of the two polymorphs of hexakis(carboxymethyl)calix[6]arene methyl ester.
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Luz et al. (2026) studied this question.
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