In
an attempt to design urea-based Janus nanocylinders through
a supramolecular approach, nonsymmetrical bis(urea)s and tris(urea)s
decorated by two incompatible polymer arms, namely, poly(styrene)
(PS) and poly(isobutylene) (PIB), were synthesized using rather straightforward
organic and polymer chemistry techniques. Light scattering experiments
revealed that these molecules self-assembled in cyclohexane by cooperative
hydrogen bonds. The extent of self-assembly was limited for the bis(urea)s.
On the contrary, reasonably anisotropic 1D structures (small nanocylinders)
could be obtained with the tris(urea)s (<i>N</i><sub>agg</sub> ∼ 50) which developed six cooperative hydrogen bonds per
molecule. <sup>1</sup>H transverse relaxation measurements and NOESY
NMR experiments in cyclohexane revealed that perfect Janus nanocylinders
with one face consisting of only PS and the other of PIB were not
obtained. Nevertheless, phase segregation between the PS and PIB chains
occurred to a large extent, resulting in patchy cylinders containing
well separated domains of PIB and PS chains. Reasons for this behavior
were proposed, paving the way to improve the proposed strategy toward
true urea-based supramolecular Janus nanocylinders