London dispersion driven compaction of coordination cages in the gas-phase - a combined ion mobility and theoretical...

Large self-assembled systems (such as metallosupramolecular rings and cages) can be difficult to structurally characterize, in particular when they show a highly dynamic behavior. In the gas-phase, Ion Mobility Spectrometry (IMS), in tandem with Electrospray Ionization Mass Spectrometry (ESI MS), can yield valuable insights into the size, shape and dynamics of such supramolecular assemblies. However, the detailed relationship between experimental IMS data and the actual gas-phase structure is still poorly understood for soft and flexible self-assemblies. In this study, we combine high resolution Trapped Ion Mobility Spectrometry (TIMS), yielding collisional cross section data (CCS), with computational modeling and theoretical CCS calculations to obtain and interpret gas-phase structural data for a series of palladium-based coordination cages. We focus on derivatives of a homoleptic lantern-shaped [Pd₂L₄]⁴⁺ cage and its interpenetrated dimer ([3X@Pd₄L₈]⁵⁺, X = Cl, Br) to study the influence of flexible side chains of different lengths, counter anions and π-stacking tendencies between the ligands in the absence of solvent. The gained insights as well as the presented CCS calculation and evaluation workflow establish a basis for the systematic gas-phase characterization of a wider range of flexible, chain-decorated and guest-modulated assemblies.