Dipole-Moment-Driven Cooperative Supramolecular Polymerization

Abstract

While the mechanism of self-assembly of π-conjugated molecules has been well studied to gain control over structure and functionality of supramolecular polymers, the intermolecular interactions underpinning it are poorly understood. Here, we study the mechanism of self-assembly of perylene bisimide derivatives possessing dipolar carbonate groups as linkers. It was observed that the combination of carbonate linkers and cholesterol/dihydrocholesterol self-assembling moieties led to a cooperative mechanism of self-assembly. Atomistic molecular dynamics simulations of an assembly in explicit solvent strongly suggest that the dipole-dipole interaction between the carbonate groups impart a macrodipolar character to the assembly. This is confirmed experimentally through the observation of a significant polarization in the bulk phase for molecules following a cooperative mechanism. The cooperativity is attributed to the presence of dipole-dipole interaction in the assembly. Thus, anisotropic long-range intermolecular interactions such as for instance, dipole-dipole interaction can serve as a way to obtain cooperative self-assembly and aid to rationalize/predict the mechanisms in various synthetic supramolecular polymers.