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Enantiopure J-Aggregate of Quaterrylene Bisimides for Strong Chiroptical NIR-Response

<p>Data to report&nbsp;https://doi.org/10.1021/jacs.3c03367:<br> Chiral polycyclic aromatic hydrocarbons can be tailored for next-generation photonic materials by carefully designing their molecular as well as supramolecular architectures. Hence, excitonic coupling can boost the chiroptical response in extended aggregates but is still challenging to achieve by pure self-assembly. Whereas most reports on these potential materials cover the UV and visible spectral range, systems in the near infrared are underdeveloped. We report a new quaterrylene bisimide derivative with a conformationally stable twisted &pi;-backbone enabled by the sterical congestion of a fourfold <em>bay</em>-arylation. Rendering the &pi;-subplanes accessible by small imide substituents allows for a slip-stacked chiral arrangement by kinetic self-assembly in low polarity solvents. The well dispersed solid-state aggregate reveals a sharp optical signature of strong J-type excitonic coupling in both, absorption (897 nm) as well as emission (912 nm) far in the NIR region and reaches absorption dissymmetry factors up to1.1&times;10^&minus;2. The structural elucidation was achieved by AFM and single-crystal X-ray analysis which we combined to derive a structural model of a fourfold stranded enantiopure superhelix. We could deduce the role of phenyl substituents not only granting stable axial chirality but also guiding the chromophore into a chiral supramolecular arrangement needed for strong excitonic chirality.</p>