Abstract

Coordination-driven self-assembly is a powerful approach for the construction of metallosupramolecules, but designing coordination moieties that can drive the self-assembly with high selectivity and specificity remains a challenge. Here we report two ortho-modified terpyridine ligands that form head-to-tail coordination complexes with Zn(II). Both complexes show narcissistic self-sorting behaviour. In addition, starting from these ligands, we obtain two sterically congested multitopic ligands and use them to construct more complex metallo-supramolecules hexagons. Because of the non-coaxial structural restrictions in the rotation of terpyridine moieties, these hexagonal macrocycles can hierarchically self-assemble into giant cyclic nanostructures via edge-to-edge stacking, rather than face-to-face stacking. Our design of dissymmetrical coordination moieties from congested coordination pairs show remarkable self-assembly selectivity and specificity.

Highlights

  • Coordination-driven self-assembly is a powerful approach for the construction of metallosupramolecules, but designing coordination moieties that can drive the self-assembly with high selectivity and specificity remains a challenge

  • The full characterization of Nuclear magnetic resonance (NMR), Electrospray ionization (ESI)-MS, and traveling wave ion mobility-mass spectrometry (TWIM-MS) confirmed that the two types of tpy moieties in ligands LA and LB could precisely self-assemble into hexagonal macrocycles through the narcissistic self-recognition mechanism

  • In summary, we have designed and synthesized a series of multitopic tpy ligands with designed coordination selectivity by ortho-modification

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Summary

Introduction

Coordination-driven self-assembly is a powerful approach for the construction of metallosupramolecules, but designing coordination moieties that can drive the self-assembly with high selectivity and specificity remains a challenge. We combined these moieties with tpy to form sterically congested multitopic ligands (LA and LB) for precise self-assembly of hexagonal macrocycles Zn9(LA)[6] and Zn12(LB)[6] (Fig. 1c). In ESI-MS (Supplementary Fig. 15A), one prominent set of peaks with charge states from 2+ to 4+ was observed (due to the loss of different numbers of PF6−).

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