Anion-assisted supramolecular polymerization of luminescent organic p-conjugated chromophores in a moderately polar solvent: tunable nanostructures and their corresponding effects on electronic properties

Supramolecular polymers of & pi;-conjugated organic chromophores have emerged as promising candidates in organic electronics because of their dynamic and highly ordered molecular organization. Herein, we demonstrate the formation of luminescent, highly conducting supramolecular polymers of a functionalized naphthalimide & pi;-chromophore-based organic semiconductor in a moderately polar organic solvent (tetrahydrofuran) by overcoming solute-solvent H-bonding via assistance from fluoride anions. The polymerization is exclusively guided by the synergistic effects of cascade H-bonding (F-MIDLINE HORIZONTAL ELLIPSISH-N- of primary amines, followed by -C00000000000000000000000000000000111111110000000011111111000000000000000000000000OMIDLINE HORIZONTAL ELLIPSISH-N- of amides), & pi;-& pi; stacking and hydrophobic interactions. An increasing molar equivalent of anions leads to a morphology transition from 1D nanowires to 2D nanosheets via nanotubes and nanorings, but above a particular threshold of the same anion, depolymerization-mediated disruption of long-range order and formation of non-luminescent spherical particles was observed. Such significant impacts of anions in supramolecular polymerization-depolymerization were utilized in modulating the electronic properties of this naphthalimide-based organic semiconductor. We presented anion assisted self-assembly of an organic semiconductor in a moderately polar solvent by overcoming solvent-solute H-bonding interactions. The morphology transition on the anion scale leads a pathway of tunable electrical conductivity.