Abstract
Two aromatic oligoamides, the 8-residue H8 and 16-residue H16, that adopt stable, cavity-containing helical conformations were examined for their complexation of a rodlike dicationic guest, octyl viologen (OV(2+)) and para-bis(trimethylammonium)benzene (TB(2+)). Studies based on 1D and 2D (1)H NMR, isothermal titration calorimetry (ITC), and X-ray crystallography demonstrated that H8 and H16 wraps around two OV(2+) ions as a double helix and a single helix, respectively, resulting in 2 : 2 and 1 : 2 complexes. Compared to H8, the longer H16 binds the OV(2+) ions with much higher binding affinity and with extraordinary negative cooperativity. In contrast to its 1 : 2 binding with OV(2+), the binding of helix H16 with the bulkier guest TB(2+) shows a 1 : 1 ratio. Host H16 also selectively binds OV(2+) in the presence of TB(2+). This novel host-guest system features pairwise placement of the otherwise strongly repulsive OV(2+) ions in the same cavity, strong negative cooperativity, and mutual adaptability of hosts and guests. The resultant complexes are highly stable [2]-, [3]-, and [4]pseudo-foldaxanes with few known precedents.