Hierarchical self-assembly driven by non-covalent interactions is a prevalent strategy employed by nature to construct sophisticated biomacromolecules, such as proteins. However, the construction of protein-like superstructures that rely on weaker dispersion forces-driven hierarchical assembly remains largely unexplored. Here, we report the first example of dispersion forces driving the high-order assembly of the lanthanide trinuclear circular helicate [HNEt₃]₃[Eu₃(L)₆] (ΔΔΔ-1) into a protein-like lanthanide octamer ((ΔΔΔ-1)₈-2).
View Article and Find Full Text PDFUndoubtably, it is challenging to simultaneously determine the identity, enantiomeric excess (ee), and total concentration of an enantiomer by just one optical measurement. Herein, we design a chiral tetrahedron Eu() with circularly polarized luminescence (CPL), which presents highly selective/stereoselective, rapid, and "turn-on" CPL response to chiral diamines, rather than the monoamino compounds, such as monoamines or amino alcohols. By recording the left- and right-CPL intensities of the Eu ion at 591 nm, the enantiomeric composition and concentration of chiral diamines can be simultaneously determined by monitoring the value and total emission intensity ( + ), respectively.
View Article and Find Full Text PDFChiral supramolecular lanthanide-helicates are regarded as promising chiroptical materials due to their combination of ground and excited state chirality and special luminescence properties from Ln, named circularly polarized luminescence (CPL). However, the sophisticated and costly asymmetric syntheses decelerate their research progress. Herein, a chiral induction strategy is employed to break the racemic equilibrium of lanthanide helicate by the formation of a compact ion pair.
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