4.8 Article

Surprising solvent-induced structural rearrangements in large [N•••I+•••N] halogen-bonded supramolecular capsules: an ion mobility-mass spectrometry study

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CHEMICAL SCIENCE
卷 9, 期 44, 页码 8343-8351

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c8sc03040e

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  1. Deutsche Forschungsgemeinscha [CRC 765]

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Coordinative halogen bonds have recently gained interest for the assembly of supramolecular capsules. Ion mobility-mass spectrometry and theoretical calculations now reveal the well-defined gas-phase structures of dimeric and hexameric [NI+N] halogen-bonded capsules with counterions located inside their cavities as guests. The solution reactivity of the large hexameric capsule shows the intriguing solvent-dependent equilibrium between the hexamer and an unprecedented pentameric [NI+N] halogen-bonded capsule, when the solvent is changed from chloroform to dichloromethane. The intrinsic flexibility of the cavitands enables this novel structure to adopt a pseudo-trigonal bipyramidal geometry with nine [NI+N] bonds along the edges and two pyridine binding sites uncomplexed.

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