Isosteric Substitutions of Urea to Thiourea and Selenourea in Aliphatic Oligourea Foldamers: Site-Specific Perturbation of the Helix Geometry

Nearly isosteric oxo to thioxo substitution was employed to interrogate the structure of foldamers with a urea backbone and explore the relationship between helical folding and hydrogen‐bonding interactions. A series of oligomers with urea bonds substituted by thiourea bonds at discrete or all positions in the sequence have been prepared and their folding propensity was studied by using a combination of spectroscopic methods and X‐ray diffraction. The outcome of oxo to thioxo replacements on the helical folding was found to depend on whether central or terminal ureas were modified. The canonical helix geometry was not affected upon insertion of thioureas close to the negative end of the helix dipole, whereas thioureas close to the positive pole were found to increase the terminal flexibility and cause helix fraying. Perturbation was amplified when a selenourea was incorporated instead, leading to a structure that is only partly folded. Positional thiourea scan was used to examine the relationship between hydrogen‐bonding interactions and helical folding in aliphatic N,N′‐linked oligourea foldamers. The influence of the oxo to thioxo replacement was found to be minimal at the negative end of the helix dipole but more pronounced at positions, in which intramolecular CS⋅⋅⋅HN bonds can be formed. A partially unfolded state predominates when a selenourea linkage is introduced instead (see figure).