Hamad, S.

Hortal, A.R.

Hurtado, P.

Martínez-Haya, B.

Oomens, J.

Steill, J.D.

Crown ethers provide a valuable benchmark for the comprehension of molecular recognition mediated by inclusion complexes. One of the most relevant crown ethers, 18-crown-6 (18c6), features a flexible six-oxygen cyclic backbone that is well-known for its selective cation binding. This study employs infrared spectroscopy and quantum mechanical calculations to elucidate the structure of the gas-phase complexes formed by the 18c6 ether with the alkali metal cations. It is shown that symmetric and chiral arrangements play a dominant role in the conformational landscape of the 18c6−alkali system. Most stable 18c6−M+ conformers are found to have symmetries C3v and C2 for Cs+, D3d for K+, C1 and D3d for Na+, and D2 for Li+. Remarkably, whereas the bare 18c6 ether is achiral, chirality emerges in the C2 and D2 18c6−M+ conformations, both of which involve pairs of stable atropoisomers capable of acting as enantiomeric selective substrates

Emergence of symmetry and chirality in crown ether complexes with alkali metal cations

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