Hexanuclear Ln6L6 Complex Formation by using an Unsymmetric Ligand

Daniel j. Bell, Tongtong Zhang, Niklas Geue, Ciarán j. Rogers, Perdita e. Barran, Alice m. Bowen, Louise s. Natrajan, Imogen a Riddell

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Multinuclear, self-assembled lanthanide complexes present clear opportunities as sensors and imaging agents. Despite the widely acknowledged potential of this class of supramolecule, synthetic and characterization challenges continue to limit systematic studies into their self-assembly restricting the number and variety of lanthanide architectures reported relative to their transition metal counterparts. Here we present the first study evaluating the effect of ligand backbone symmetry on multinuclear lanthanide complex self-assembly. Replacement of a symmetric ethylene linker with an unsymmetric amide at the centre of a homoditopic ligand governs formation of an unusual Ln6L6 complex with coordinatively unsaturated metal centres. The choice of triflate as a counterion, and the effect of ionic radii are shown to be critical for formation of the Ln6L6 complex. The atypical Ln6L6 architecture is characterized using a combination of mass spectrometry, luminescence, DOSY NMR and EPR spectroscopy measurements. Luminescence experiments support clear differences between comparable Eu6L6 and Eu2L3 complexes, with relatively short luminescent lifetimes and low quantum yields observed for the Eu6L6 structure indicative of non-radiative decay processes. Synthesis of the Gd6L6analogue allows three distinct Gd···Gd distance measurements to be extracted using homo-RIDME EPR experiments.
Original languageEnglish
Article numbere202302497
JournalChemistry – A European Journal
Early online date21 Sept 2023
Publication statusE-pub ahead of print - 21 Sept 2023


  • Self-assembly
  • lanthanide
  • polynuclear
  • unsymmetric ligand
  • luminescence


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