Chirality delivers substantial value
to the field of supramolecular
polymers, not only serving as a probe to monitor the dynamic assembly
process but providing access to chiroptical materials. The current
study demonstrates that, for supramolecular donor–acceptor
copolymers, their comonomer organization modes can be greatly influenced
by stereocommunication at the molecular level. The enantiopure N-[(1R or 1S)-phenylethyl]benzamides
are incorporated into two structurally similar comonomers, locating
between the π-aromatic diethynylacene core and the alkyl chain
peripheries. Parallel arrangement of the stereogenic methyl units
brings steric hindrance between the homochiral comonomers, which is
relieved for the heterochiral comonomers due to the adoption of staggered
arrangement. It consequently steers randomly mixed organization for
the homochiral supramolecular copolymers within the nanofibers. In
comparison, the heterochiral counterparts form nanoparticles in an
alternate donor–acceptor organization manner. The variation
of comonomer arrangement modes gives rise to distinct energy transfer
efficiency at the supramolecular level. Overall, the elaborate manipulation
of stereogenic centers in the comonomer structures exerts significant
impacts on the characteristics of supramolecular copolymers, which
could be useful for chiral sensing, recognition, and optoelectronic
applications.