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Octameric near-IR dye nanoclusters are produced by complexation of potassium cations with a phthalocyanine–guanosine conjugate. The combination of hydrogen-bonding, K+ coordination, π–π stacking and steric interactions between the chiral side groups is responsible for defining a specific helical chromophore arrangement in the clusters, which display high stability and maintain their supramolecular identity onto substrates.

Graphical abstract: Well-defined, persistent, chiral phthalocyanine nanoclusters via G-quadruplex assembly

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