Sequence-defined chiral polyimides comprising identical asymmetric diamine monomers arranged in different directions along the main chain were designed and prepared. These new sequence-defined polymers exhibit sequence-dependent self-assembly behaviors and responses to ibuprofen enantiomers, as revealed by their chiroptical spectra and gelation properties. For the first time, the self-assembly of polymers and their interactions with guest molecules have been successfully controlled by means of the directional arrangement of the monomers in their polymer backbones.
Keywords: chiral polyimide; circular dichroism; molecular recognition; self-assembly; sequence-defined polymer.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.