AI Article Synopsis

  • A crystallographic study of host-guest complexes in cubic M L coordination cages revealed that some organic guests form unexpected 1:2 complexes instead of the expected 1:1 complexes.
  • Despite solution titrations suggesting 1:1 complex formation, further analysis indicated that certain guests can bind in pairs, showcasing complexities in how these interactions are understood.
  • This finding not only raises questions about the stoichiometry of supramolecular complexes but also suggests potential changes in the reactivity of the bound guests.

Article Abstract

A crystallographic investigation of a series of host-guest complexes in which small-molecule organic guests occupy the central cavity of an approximately cubic M L coordination cage has revealed some unexpected behaviour. Whilst some guests form 1:1 H⋅G complexes as we have seen before, an extensive family of bicyclic guests-including some substituted coumarins and various saturated analogues-form 1:2 H⋅G complexes in the solid state, despite the fact that solution titrations are consistent with 1:1 complex formation, and the combined volume of the pair of guests significantly exceeds the Rebek 55±9 % packing for optimal guest binding, with packing coefficients of up to 87 %. Re-examination of solution titration data for guest binding in two cases showed that, although conventional fluorescence titrations are consistent with 1:1 binding model, alternative forms of analysis-Job plot and an NMR titration-at higher concentrations do provide evidence for 1:2 H⋅G complex formation. The observation of guests binding in pairs in some cases opens new possibilities for altered reactivity of bound guests, and also highlights the recently articulated difficulties associated with determining stoichiometry of supramolecular complexes in solution.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079040PMC
http://dx.doi.org/10.1002/chem.201905499DOI Listing

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