“…The most prominent example is DNA, which is a polymer consisting of achiral bases linked to a chiral backbone containing deoxyribose, thus giving rise to a homohelical macrostructure . Inspired by this, many artificial homohelical polymers consisting of a wide variety of different parent monomer structures have been synthesized and studied, − includingbut not limited tophenylene ethynylenes, − thiophenes, − indolocarbazoles, aromatic amides, − porphyrins, synthetic peptides, , bi- , and terpyridines, terphenyls, , isocyanates, − isocyanides, − silanes, , and acetylenes. − The homohelicity in these foldamers was realized using different approaches. Apart from utilizing intrinsically chiral monomers to construct the main chain, − an excess in preferred screw sense can be attained by the introduction of a chiral guest molecule, ,,, the use of chiral solvents, using chiral terminal groups, ,,, asymmetric polymerization, , chiral resolution, ,, or the incorporation of chiral units into the main chain. ,, However, one of the most established methods is the addition of an element of chirality onto the peripheral side chain, which then promo...…”