Synthesis and Stacked Conformations of Symmetrical and Unsymmetrical Oligo-ureas of Metaphenylenediamine

The addition of substituted anilines to nitro-substituted isocyanates followed by reduction generates new
aniline-substituted ureas, which can be further extended in a one- or two-directional iterative manner to
form oligomeric ureas based on a m-phenylenediamine monomer. Oligo-ureas with up to eight urea linkages
are reported. Fully N-substituted oligo-ureas are crystalline, and the X-ray crystal structures display ring-stacked conformations. 1H NMR studies indicate that the stacked conformation persists in solution.