Noncovalent macromolecular architectures of oligo(p-phenylenevinylene)s (OPVs): Role of end functional groups on the gelation of organic solvents

Abstract

Self-assembly of a few OPV derivatives having different end functional groups to aggregates, fibrous networks and organogels are discussed. OPV1 and OPV2 functionalized with ester moieties form gels in nonpolar hydrocarbon solvents whereas OPV3 with carboxylic acid groups form gel from THF and dichloromethane. OPV4 with dicyano moieties form aggregates but could not gelate solvents. AFM and TEM studies revealed considerable difference in the morphology of the self-assembled structures of OPVi-4. From the optical, morphological and gelation data it is concluded that the nature of the end functional groups strongly influences upon the self-assembly and gelation properties of OPVs.