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    Reversible Transformation of a One-Handed Helical Foldamer Utilizing a Planarity-Switchable Spacer and <i>C</i><sub>2</sub>‑Chiral Spirobifluorene Units

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    Polymeric quaterthiophenes containing optically active <i>C</i><sub>2</sub>-chiral spirobifluorene skeletons were synthesized as a new type of helical foldamers, and their higher-order structures were investigated. Oxidization of quaterthiophene moieties caused the spacer units to be in planar structure, leading the conformation of the polymer to be a coil-shaped, rigid helix. This transformation was reversibly performed
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