The
optoelectronic properties of conjugated polymers are dictated
by their chain conformations, which depend on the interplay of delocalization
of electrons along the π-conjugated backbone and the intrachain
interactions of pendant side chains. Here, we leverage small-angle
neutron scattering to measure the chain shapes of several classes
of commonly used, high mobility donor–acceptor conjugated polymers
in dilute solution. We find that these model conjugated polymers are
semiflexible with persistence lengths ranging from several to hundreds
of nanometers, dependent on the molecular structure of the polymer,
indicating the importance of repeat unit geometry, particularly side-chain
size and branching, on the overall chain conformations. The measured
persistence lengths show good agreement with those calculated according
to dihedral distributions predicted from density functional theory.
Larger persistence lengths are shown to correlate with increased charge-carrier
mobility, signifying the importance of rational molecular design to
obtain high persistence length organic semiconductors and thus advantageous
optoelectronic properties.